AU2013200389A1 - Kinase antagonists - Google Patents

Abstract

The present invention provides novel compounds that are antagonists of P13 kinase, P13 kinase and tryosine kinase, PDKinase and mTOR, or PI3Kinase, mTOR and tryosine kinase. WO 2007/114926 PCT/US2007/008395 Ap P1(Bx= L-53 noe 1-O oe 0 PIK-39 x-ray K-593 x-ray P1K-10a model 2.2A A 3.1 A3.A PI-103

Description

AUSTRALIA Regulation 3.2 Patents Act 1990 Complete Specification Standard Patent Divisional APPLICANT: The Regents of the University of California Invention Title: KINASE ANTAGONISTS The following statement is a full description of this invention, including the best method of performing it known to me: WO 2007/114926 PCT/US2007/008395 KINASE ANTAGONISTS CROSS-REFERENCES TO RELATED APPLICATIONS 10001] This application claims the benefit of U.S. Provisional Patent Application No. 60/744,269, filed April 4,2006, and U.S. Provisional Patent Application No. 60/744,270, 5 filed April 4, 2006, both of which are incorporated herein by reference in their entirety for all purposes. STATEMENT AS TO RIGHTS TO INVENTIONS MADE UNDER FEDERALLY SPONSORED RESEARCH AND DEVELOPMENT [00021 The present invention was supported by a grant from the National Institutes of 0 Health (AI44009). The Government has certain rights to the invention. BACKGROUND OF THE INVENTION [0003] Phosphoinositide 3-kinases (P13-Ks) catalyze the synthesis of the phosphatidylinositol (PI) second messengers PI(3)P, PI(3,4)P2, and PI(3,4,5)P3 (PIP3) (Fruman et al., 1998). In the appropriate cellular context, these three lipids control diverse 5 physiological processes including cell growth, survival, differentiation and chemotaxis (Katso et al., 2001). The P13-K family comprises 15 kinases with distinct substrate specificities, expression patterns, and modes of regulation (Katso et al., 2001). The class I P13-Ks (p1 10a, p1 10p, p1 108, and p1 10y) are activated by tyrosine kinases or G-protein coupled receptors to generate PIP3, which engages downstream effectors such as the L0 Akt/PDK1 pathway, the Tec family kinases, and the Rho family GTPases. The class II and III P13-Ks play a key role in intracellular trafficking through the synthesis of PI(3)P and PI(3,4)P2. The PIKKs are protein kinases that control cell growth (mTORCl) or monitor genomic integrity (ATM, ATR, DNA-PK, and hSmg-1). [00041 The importance of these enzymes in diverse pathophysiology has made the P13-K 25 family the focus of intense interest as a new class of drug targets (Ward et al., 2003). This interest has been fueled by the recent discovery that p1Oa is frequently mutated in primary tumors (Samuels et al., 2004) and evidence that the lipid phosphatase PTEN, an inhibitor of P13-K signaling, is a commonly inactivated tumor suppressor (Cantley and Neel, 1999). Efforts are underway to develop small molecule P13-K inhibitors for the treatment of 30 inflammation and autoimmune disease (p1 10S, p1 10y, and mTOR), thrombosis (p110p), viral infection (the PIKKs) and cancer (p11 Oa, mTOR, and others). Recently, the first selective 1 WO 2007/114926 PCT/US2007/008395 inhibitors of these enzymes have been reported (Camps et al., 2005; Condliffe et al., 2005; Jackson et al., 2005; Knight et al., 2004; Lau et al., 2005; Sadhu et al., 2003). [0005] Protein tyrosine kinases, protein serine/threonine kinases, and lipid kinases are distinct classes of proteins that play critical roles in regulation and proliferation of cellular 5 activity. Small molecules that inhibit these protein classes have the potential to disrupt dysfunctiona/pathological pathways at two distinct points. For example, signaling through tyrosine kinase receptors is known to be disregulated in several types of cancer. This signaling pathway involves downstream proteins such as P13 Kinase. Signaling through the serine/threonine protein kinase mTOR (also known as the mammalian target of rapamycin) is 0 known to regulate cell growth, cell proliferation, cell motility, cell survival, protein synthesis, and transcription. Disruption of the mTOR pathway is implicated as a contributing factor to various human disease processes, especially various types of cancer. An inhibitor that blocks activity of protein tyrosine kinase and P13 Kinase, mTOR and PI3Kinase, or mTOR, protein tyrosine kinase and P13 Kinase, has the potential to stop the aberrant signaling at two or three 5 different levels. Double or triple inhibition by a small molecule may magnify drug potency, increasing the compound's therapeutic potential. [00061 The present invention meets these and other needs in the art by providing a new class of P13 kinase antagonists, P13 kinase and tryosine kinase antagonists, PI3Kinase and mTOR antagonists, and PI3Kinase, mTOR and tryosine kinase antagonists. 0 BRIEF SUMMARY OF THE INVENTION [00071 It has been discovered that certain compounds described herein are potent antagonists of P13 kinase, PI3 kinase and tryosine kinase, PI3Kinase and mTOR, or PI3Kinase, mTOR and tryosine kinase. [0008] In one aspect, the present invention provides novel kinase antagonists that are P13 25 Kinase affinity pocket binding antagonists (e.g. a P13-Kinase affinity pocket binding pyrazolopyrimidine antagonist or a P13-Kinase affinity pocket binding pyrrolopyrimidine antagonist). The P13-Kinase affinity pocket binding antagonist is a compound containing a P13-Kinase affinity pocket binding moiety. The P13-Kinase affinity pocket binding pyrazolopyrimidine antagonists of the present invention are substituted pyrazolopyrimidine W compounds containing a P13-Kinase affinity pocket binding moiety. Likewise, the P13 Kinase affinity pocket binding pyrrolopyrimidine antagonists of the present invention are 2 WO 2007/114926 PCT/US2007/008395 substituted pyrrolopyrimidine compounds containing a P13-Kinase affinity pocket binding moiety. [00091 In another aspect, the present invention provides the novel kinase antagonists of Formula (I), defined below. 5 [00101 In another aspect, the present invention provides methods of decreasing the catalytic activity of a P13 Kinase (e.g. a p110 kinase). The method includes the step of contacting said P13 kinase with an activity decreasing amount of a compound of the present invention (i.e. a P13-Kinase affinity pocket binding antagonists, or an antagonist of Formula I). [00111 In another aspect, the present invention provides a method of treating a condition 0 mediated by P13 kinase activity, PI3 Kinase activity and tyrosine Kinase Activity, P13 Kinase activity and mTOR activity, or P13 Kinase activity, tyrosine kinase activity, and mTOR activity in a subject in need of such treatment. The method includes administering to the subject a therapeutically effective amount of a compound of the present invention (i.e. a P13 Kinase affinity pocket binding antagonists, or an antagonist of Formula I). 5. BRIEF DESCRIPTION OF THE DRAWINGS [00121 Figure 1 illustrates structures of representative compounds from eleven chemotypes of P13-K inhibitors. [0013] Figure 2 illstrates structures of isoform-selective P13-K inhibitors. A. Structure of ATP in the active site of p1 10y, highlighting different regions of the ATP binding pocket. B. 20 An alignment of all reported P13-K inhibitor co-crystal structures. Met 804 adopts an up conformation in all structures except PIK-39. C. Structures or models of isoform-selective P13-K inhibitors bound to p110y. D. Structures or models of multi-targeted PI3-K inhibitors bound to p110y. [0014] Figure 3 illustrates the probing of selectivity and an the PI3-Kinase affinity pocket. 25 A. The structure of PIK-39 bound to p11 Oy suggests a model for the binding of IC87114. PIK-293 and PIK-294 are pyrazolopyrimidine analogs of IC87114. PIK-294 projects am phenol into the affinity pocket, and this compound is more potent against the class I P13-Ks. B. (Left) Ratio of IC50 values between mutant and wild-type for p1108 inhibitors and p11 Oc/multi-targeted inhibitors. (Center) Dose response curves for binding of two p1103 30 inhibitors to wild-type, M752I, and M752V p1108 (Right) Models suggesting the impact of 3 WO 2007/114926 PCT/US2007/008395 the M7521 and M752V mutations in p1 108 on the binding of the different classes of inhibitors. 100151 Figure 4. Structures of additional P13-K inhibitors and inactive analogs. [0016] Figure 5. IC50 values (pM) for selected P13-K inhibitors against lipid kinases. 5 [00171 Figure 6. Inhibition of protein kinases by P13-K inhibitors. Values represent % activity remaining in the presence of 10 pM inhibitor. Values are average of triplicate measurements. IC50 values are in parenthesis where appropriate (pM). [0018] Figure 7 sets forth the sequence of a human p110S kinase. [0019] Figure 8 sets forth the sequence of a human p11 Oy kinase. ) [0020] Figure 9 sets forth the sequence of a human p11O(x kinase. [0021] Figure 10 sets forth the sequence of a human p1 10p kinase. DETAILED DESCRIPTION OF THE INVENTION I. Definitions [0022] Abbreviations used herein have their conventional meaning within the chemical and i biological arts. [0023] Where substituent groups are specified by their conventional chemical formulae, written from left to' right, they equally encompass the chemically identical substituents that would result from writing the structure from right to left, e.g., -CH 2 0- is equivalent to

-OCH

2

-

0 [00241 The term "alkyl," by itself or as part of another substituent, means, unless otherwise stated, a straight (i.e. unbranched) or branched chain, or cyclic hydrocarbon radical, or combination thereof, which may be fully saturated, mono- or polyunsaturated and can include di- and multivalent radicals, having the number of carbon atoms designated (i.e. C 1

-C

10 means one to ten carbons). Examples of saturated hydrocarbon radicals include, but are not 5 limited to, groups such as methyl, ethyl, n-propyl, isopropyl, n-butyl, t-butyl, isobutyl, sec butyl, cyclohexyl, (cyclohexyl)methyl, cyclopropylmethyl, homologs and isomers of, for example, n-pentyl, n-hexyl, n-heptyl, n-octyl, and the like. An unsaturated alkyl group is one having one or more double bonds or triple bonds. Examples of unsaturated alkyl groups 4 WO 2007/114926 PCT/US2007/008395 include, but are not limited to, vinyl, 2-propenyl, crotyl, 2-isopentenyl, 2-(butadienyl), 2,4 pentadienyl, 3-(1,4-pentadienyl), ethynyl, 1- and 3-propynyl, 3-butynyl, and the higher homologs and isomers. [0025] The term "alkylene" by itself or as part of another substituent means a divalent 5 radical derived from an alkyl, as exemplified, but not limited, by -CH 2

CH

2

CH

2

CH

2 -,

-CH

2

CH=CHCH

2 -, -CH 2

C=CCH

2 -, -CH 2

CH

2

CH(CH

2

CH

2

CH

3

)CH

2 -. Typically, an alkyl (or alkylene) group will have from 1 to 24 carbon atoms, with those groups having 10 or fewer carbon atoms being preferred in the present invention. A "lower alkyl" or "lower alkylene" is a shorter chain alkyl or alkylene group, generally having eight or fewer carbon atoms. 0 [00261 The term "heteroalkyl," by itself or in combination with another term, means, unless otherwise stated, a stable straight or branched chain, or cyclic hydrocarbon radical, or combinations thereof, consisting of at least one carbon atoms and at least one heteroatom selected from the group consisting of 0, N, P, Si and S, and wherein the nitrogen, phosphorus, and sulfur atoms may optionally be oxidized and the nitrogen heteroatom may 5 optionally be quaternized. The heteroatom(s) 0, N, P and S and Si may be placed at any interior position of the heteroalkyl group or at the position at which alkyl group is attached to the remainder of the molecule. Examples include, but are not limited to, -CH 2

-CH

2 -0-CH 3 ,

-CH

2

-CH

2

-NH-CH

3 , -CH 2

-CH

2

-N(CH

3

)-CH

3 , -CH 2

-S-CH

2

-CH

3 , -CH 2

-CH

2

,-S(O)-CH

3 ,

-CH

2

-CH

2 -S(0) 2

-CH

3 , -CH=CH-0-CH 3 , -Si(CH 3

)

3 , -CH 2

-CH=N-OCH

3 , -CH=CH-N(CH 3

)

0 CH 3 , 0-CH 3 , -O-CH 2

-CH

3 , and -CN. Up to two or three heteroatoms may be consecutive, such as, for example, -CH 2

-NH-OCH

3 and -CH 2 -0-Si(CH 3

)

3 . Similarly, the term - "heteroalkylene" by itself or as part of another substituent means a divalent radical derived from heteroalkyl, as exemplified, but not limited by, -CH 2

-CH

2

-S-CH

2

-CH

2 - and -CH 2

-S

CH

2

-CH

2

-NH-CH

2 -. For heteroalkylene groups, heteroatoms can also occupy either or both 25 of the chain termini (e.g., alkyleneoxo, alkylenedioxo, alkyleneamino, alkylenediamino, and the like). Still further, for alkylene and heteroalkylene linking groups, no orientation of the linking group is implied by the direction in which the formula of the linking group is written. For example, the formula -C(O)OR'- represents both -C(O)OR'- and -R'OC(O)-. As described above, heteroalkyl groups, as used herein, include those groups that are attached to 30 the remainder of the molecule through a heteroatom, such as -C(O)R', -C(O)NR', -NR'R7, OR', -SR', and/or -S0 2 R'. Where "heteroalkyl" is recited, followed by recitations of specific heteroalkyl groups, such as -NR'R" or the like, it will be understood that the terms heteroalkyl 5 WO 2007/114926 PCT/US2007/008395 and -NR'R" are not redundant or mutually exclusive. Rather, the specific heteroalkyl groups are recited to add clarity. Thus, the term "heteroalkyl" should not be interpreted herein as excluding specific heteroalkyl groups, such as -NR'R" or the like. [0027] The terms "cycloalkyl" and "heterocycloalkyl", by themselves or in combination 5 with other terms, represent, unless otherwise stated, cyclic versions of alkyll" and "heteroalkyl", respectively. Additionally, for heterocycloalkyl, a heteroatom can occupy the position at which the heterocycle is attached to the remainder of the molecule. Examples of cycloalkyl include, but are not limited to, cyclopentyl, cyclohexyl, 1-cyclohexenyl, 3 cyclohexenyl, cycloheptyl, and the like. Examples of heterocycloalkyl include, but are not 0 limited to, 1 -(1,2,5,6-tetrahydropyridyl), 1-piperidinyl, 2-piperidinyl, 3-piperidinyl, 4 morpholinyl, 3-morpholinyl, tetrahydrofuran-2-yl, tetrahydrofuran-3-yl, tetrahydrothien-2-yl, tetrahydrothien-3-yl, 1 -piperazinyl, 2-piperazinyl, and the like. The terms "cycloalkylene" and "heterocycloalkylene" refer to the divalent derivatives of cycloalkyl and heterocycloalkyl, respectively. 5 [0028] The terms "halo" or "halogen," by themselves or as part of another substituent, mean, unless otherwise stated, a fluorine, chlorine, bromine, or iodine atom. Additionally, terms such as "haloalkyl," are meant to include monohaloalkyl and polyhaloalkyl. For example, the term "halo(C1-C 4 )alkyl" is mean to include, but not be limited to, trifluoromethyl, 2,2,2-trifluoroethyl, 4-chlorobutyl, 3-bromopropyl, and the like. 0 [0029] The term "aryl" means, unless otherwise stated, a polyunsaturated, aromatic, hydrocarbon substituent which can be a single ring or multiple rings (preferably from 1 to 3 rings) which are fused together (e.g. naphthyl) or linked covalently. The term "heteroaryl" refers to aryl groups (or rings) that contain from one to four heteroatoms (in each separate ring in the case of multiple rings) selected from N, 0, and S, wherein the nitrogen and sulfur .5 atoms are optionally oxidized, and the nitrogen atom(s) are optionally quaternized. A heteroaryl group can be attached to the remainder of the molecule through a carbon or heteroatom. Non-limiting examples of aryl and heteroaryl groups include phenyl, 1-naphthyl, 2-naphthyl, 4-biphenyl, 1-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl, 3-pyrazolyl, 2-imidazolyl, 4 imidazolyl, pyrazinyl, 2-oxazolyl, 4-oxazolyl, 2-phenyl-4-oxazolyl, 5-oxazolyl, 3-isoxazolyl, 0 4-isoxazolyl, 5-isoxazolyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 2-furyl, 3-furyl, 2-thienyl, 3 thienyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, 2-pyrimidyl, 4-pyrimidyl, 5-benzothiazolyl, purinyl, 2-benzimidazolyl, 5-indolyl, 1-isoquinolyl, 6-isoquinolyl, 2-quinoxalinyl, 5-quinoxalinyl, 3 6 WO 2007/114926 PCT/US2007/008395 quinolyl, and 6-quinolyl. Thus, the term "heteroaryl" include fused ring structures in which at least one ring includes at least two double bonds. Substituents for each of above noted aryl and heteroaryl ring systems are selected from the group of acceptable substituents described below. The terms "arylene" and "heteroarylene" refer to the divalent radicals of aryl and 5 heteroaryl, respectively. [0030] For brevity, the term "aryl" when used in combination with other terms (e.g., aryloxo, arylthioxo, arylalkyl) includes both aryl and heteroaryl rings as defined above. Thus, the term "arylalkyl" is meant to include those radicals in which an aryl group is attached to an alkyl group (e.g., benzyl, phenethyl, pyridyhnethyl and the like) including 0 those alkyl groups in which a carbon atom (e.g., a methylene group) has been replaced by, for example, an oxygen atom (e.g., phenoxymethyl, 2-pyridyloxymethyl, 3-(1 naphthyloxy)propyl, and the like). However, the term "haloaryl," as used herein is meant to cover only aryls substituted with one or more halogens. [0031] Where a heteroalkyl, heterocycloalkyl, or heteroaryl includes a specific number of 5 members (e.g. "3 to 7 membered"), the term "member" referrers to a carbon or heteroatom. [00321 The term "oxo" as used herein means an oxygen that is double bonded to a carbon atom. [0033] Each of above terms (e.g., "alkyl," "heteroalkyl," "cycloalkyl, and "heterocycloalkyl", "aryl," "heteroaryl" as well as their divalent radical derivatives) are 3 meant to include both substituted and unsubstituted forms of the indicated radical. Preferred substituents for each type of radical are provided below. [0034] Substituents for alkyl, heteroalkyl, cycloalkyl, heterocycloalkyl monovalent and divalent derivative radicals (including those groups often referred to as alkylene, alkenyl, heteroalkylene, heteroalkenyl, alkynyl, cycloalkyl, heterocycloalkyl, cycloalkenyl, and 5 heterocycloalkenyl) can be one or more of a variety of groups selected from, but not limited to: -OR', =0, =NR', =N-OR', -NR'R", -SR', -halogen, -SiR'R"R"', -OC(O)R', -C(O)R', -CO2R',-C(O)NR', -OC(O)NR!', -NR"'C(O)R', -NR'-C(O)NR"'I, -NR"'C(O)OR', -NR-C(NR'R")=NR", -S(O)R', -S(O) 2 R', -S(O) 2 NR'R", -NRSO 2 R', -CN and -NO 2 in a number ranging from zero to (2m'+1), where m' is the total number of carbon atoms in such 0 radical. R', R", R"' and R"" each preferably independently refer to hydrogen, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted 7 WO 2007/114926 PCT/US2007/008395 'heterocycloalkyl, substituted or unsubstituted aryl (e.g., aryl substituted with 1-3 halogens), substituted or unsubstituted alkyl, alkoxy or thioalkoxy groups, or arylalkyl groups. As used herein, an "alkoxy" group is an alkyl attached to the remainder of the molecule through a divalent oxygen radical. When a compound of the invention includes more than one R group, 5 for example, each of the R groups is independently selected as are each R', R", R'" and R"" groups when more than one of these groups is present. When R' and R" are attached to the same nitrogen atom, they can be combined with the nitrogen atom to form a 4-, 5-, 6-, or 7 membered ring. For example, -NR'R" is meant to include, but not be limited to, 1 pyrrolidinyl and 4-morpholinyl. From the above discussion of substituents, one of skill in the 0 art will understand that the term alkyll" is meant to include groups including carbon atoms bound to groups other than hydrogen groups, such as haloalkyl (e.g., -CF 3 and -CH 2

CF

3 ) and acyl (e.g., -C(O)CH 3 , -C(O)CF 3 , -C(O)CH 2

OCH

3 , and the like). [0035] Similar to the substituents described for alkyl radicals above, exemplary substituents for aryl and heteroaryl groups ( as well as their divalent derivatives) are varied and are 5 selected from, for example: halogen, -OR', -NR'R", -SR', -halogen, -SiR'R"R"', -OC(O)R', -C(O)R', -CO 2 R', -C(O)NR'R", -OC(O)NR'R", -NR"C(O)R', -NR'-C(O)NR"R"', -NR"'C(O)OR', -NR-C(NR'R"')=NR"", -NR-C(NRR)=NR'"., -S(O)R', -S(O)2R',

-S(O)

2 NR'R", -NRSO 2 R', -CN and -NO 2 , -R', -N 3 , -CH(Ph)2, fluoro(C-C 4 )alkoxo, and fluoro(C-C4)alkyl, in a number ranging from zero to the total number of open valences on 0 aromatic ring system; and where R', R", R!" and R"" are preferably independently selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl and substituted or unsubstituted heteroaryl. When a compound of the invention includes more than one R group, for example, each of the R 25 groups is independently selected as are each R', R", R'" and R"" groups when more than one of these groups is present. [0036] Two of the substituents on adjacent atoms of aryl or heteroaryl ring may optionally form a ring of the formula -T-C(O)-(CRR')-U-, wherein T and U are independently -NR-, -0-, -CRR'- or a single bond, and q is an integer of from 0 to 3. Alternatively, two of the 30 substituents on adjacent atoms of aryl or heteroaryl ring may optionally be replaced with a substituent of the formula -A-(CH 2 )r-B-, wherein A and B are independently -CRR'-, -0-, -NR-, -S-, -S(O)-, -S(O) 2 -, -S(O) 2 NR'- or a single bond, and r is an integer of from 1 to 4. 8 WO 2007/114926 PCT/US2007/008395 One of the single bonds of the new ring so formed may optionally be replaced with a double bond. Alternatively, two of the substituents on adjacent atoms of aryl or heteroaryl ring may optionally be replaced with a substituent of the formula -(CRR')-X'-(C"R'")d-, where s and d are independently integers of from 0 to 3, and X' is -0-, -NR'-, -S-, -S(O)-, -S(0)2-, or 5 -S(O) 2 NR'-. The substituents R, R', R" and R"' are preferably independently selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, and substituted or unsubstituted heteroaryl. 100371 As used herein, the term "heteroatom" or "ring heteroatom" is meant to include 0 oxygen (0), nitrogen (N), sulfur (S), phosphorus (P), and silicon (Si). [00381 An "aminoalkyl" as used herein refers to an amino group covalently bound to an alkylene linker. The amino group is -NR'R", wherein R' and R" are typically selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, 5 substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl. [0039] A "substituent group," as used herein, means a group selected from the following moieties: [0040] (A) -OH, -NH 2 , -SH, -CN, -CF 3 , -NO 2 , oxo, halogen, unsubstituted alkyl, unsubstituted heteroalkyl, unsubstituted cycloalkyl, unsubstituted heterocycloalkyl, 0 unsubstituted aryl, unsubstituted heteroaryl, and [0041] (B) alkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl, substituted with at least one substituent selected from: [0042] (i) oxo, -OH, -NH 2 , -SH, -CN, -CF 3 , -NO 2 , halogen, unsubstituted alkyl, unsubstituted heteroalkyl, unsubstituted cycloalkyl, unsubstituted heterocycloalkyl, 5 unsubstituted aryl, unsubstituted heteroaryl, and [0043] (ii) alkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl, substituted with at least one substituent selected from: [0044] (a) oxo, -OH, -NH 2 , -SH, -CN, -CF 3 , -NO 2 , halogen, unsubstituted alkyl, unsubstituted heteroalkyl, unsubstituted cycloalkyl, unsubstituted heterocycloalkyl, 0 unsubstituted aryl, unsubstituted heteroaryl, and 9 WO 2007/114926 PCT/US2007/008395 [0045] (b) alkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl, substituted with at least one substituent selected from oxo, -OH, -NH 2 , -SH, -CN, -CF 3 , -NO 2 , halogen, unsubstituted alkyl, unsubstituted heteroalkyl, unsubstituted cycloalkyl, unsubstituted heterocycloalkyl, unsubstituted aryl, and unsubstituted heteroaryl. 5 [00461 A "size-limited substituent" or " size-limited substituent group," as used herein means a group selected from all of the substituents described above for a "substituent group," wherein each substituted or unsubstituted alkyl is a substituted or unsubstituted C-C 2 0 alkyl, each substituted or unsubstituted heteroalkyl is a substituted or unsubstituted 2 to 20 membered heteroalkyl, each substituted or unsubstituted cycloalkyl is a substituted or 0 unsubstituted C 4

-C

8 cycloalkyl, and each substituted or unsubstituted heterocycloalkyl is a substituted or unsubstituted 4 to 8 membered heterocycloalkyl. [0047] A "lower substituent" or " lower substituent group," as used herein means a group selected from all of the substituents described above for a "substituent group," wherein each substituted or unsubstituted alkyl is a substituted or unsubstituted CI-Cs alkyl, each 5 substituted or unsubstituted heteroalkyl is a substituted or unsubstituted 2 to 8 membered heteroalkyl, each substituted or unsubstituted cycloalkyl is a substituted or unsubstituted C 5 C 7 cycloalkyl, and each substituted or unsubstituted heterocycloalkyl is a substituted or unsubstituted 5 to 7 membered heterocycloalkyl. [00481 The compounds of the present invention may exist as salts. The present invention 0 includes such salts. Examples of applicable salt forms include hydrochlorides, hydrobromides, sulfates, methanesulfonates, nitrates, maleates, acetates, citrates, fumarates, tartrates (eg (+)-tartrates, (-)-tartrates or mixtures thereof including racemic mixtures, succinates, benzoates and salts with amino acids such as glutamic acid. These salts may be prepared by methods known to those skilled in art. Also included are base addition salts such 25 as sodium, potassium, calcium, ammonium, organic amino, or magnesium salt, or a similar salt. When compounds of the present invention contain relatively basic functionalities, acid addition salts can be obtained by contacting the neutral form of such compounds with a sufficient amount of the desired acid, either neat or in a suitable inert solvent. Examples of acceptable acid addition salts include those derived from inorganic acids like hydrochloric, 10 hydrobromic, nitric, carbonic, monohydrogencarbonic, phosphoric, monohydrogenphosphoric, dihydrogenphosphoric, sulfuric, monohydrogensulfuric, hydriodic, or phosphorous acids and the like, as well as the salts derived organic acids like 10 WO 2007/114926 PCT/US2007/008395 acetic, propionic, isobutyric, maleic, malonic, benzoic, succinic, suberic, fumaric, lactic, mandelic, phthalic, benzenesulfonic, p-tolylsulfonic, citric, tartaric, methanesulfonic, and the like. Also included are salts of amino acids such as arginate and the like, and salts of organic acids like glucuronic or galactunoric acids and the like. Certain specific compounds of the 5 present invention contain both basic and acidic functionalities that allow the compounds to be converted into either base or acid addition salts. [0049] The neutral forms of the compounds are preferably regenerated by contacting the salt with a base or acid and isolating the parent compound in the conventional manner. The parent form of the compound differs from the various salt forms in certain physical 0 properties, such as solubility in polar solvents. [00501 Certain compounds of the present invention can exist in unsolvated forms as well as solvated forms, including hydrated forms. In general, the solvated forms are equivalent to unsolvated forms and are encompassed within the scope of the present invention. Certain compounds of the present invention may exist in multiple crystalline or amorphous forms. In 5 general, all physical forms are equivalent for the uses contemplated by the present invention and are intended to be within the scope of the present invention. [00511 Certain compounds of the present invention possess asymmetric carbon atoms (optical or chiral centers) or double bonds; the enantiomers, racemates, diastereomers, tautomers, geometric isomers, stereoisometric forms that may be defined, in terms of absolute o stereochemistry, as (R)-or (S)- or, as (D)- or (L)- for amino acids, and individual isomers are encompassed within the scope of the present invention. The compounds of the present invention do not include those which are known in art to be too unstable to synthesize and/or isolate. The present invention is meant to include compounds in racemic and optically pure forms. Optically active (R)- and (S)-, or (D)- and (L)-isbmers may be prepared using chiral 25 synthons or chiral reagents, or resolved using conventional techniques. When the compounds described herein contain olefinic bonds or other centers of geometric asymmetry, and unless specified otherwise, it is intended that the compounds include both E and Z geometric isomers. [00521 The term "tautomer," as used herein, refers to one of two or more structural isomers 30 which exist in equilibrium and which are readily converted from one isomeric form to another. 11 WO 2007/114926 PCT/US2007/008395 [00531 It will be apparent to one skilled in the art that certain compounds of this invention may exist in tautomeric forms, all such tautomeric forms of the compounds being within the scope of the invention. [0054] Unless otherwise stated, structures depicted herein are also meant to include all 5 stereochemical forms of the structure; i.e., the R and S configurations for each asymmetric center. Therefore, single stereochemical isomers as well as enantiomeric and diastereomeric mixtures of the present compounds are within the scope of the invention. [0055] Unless otherwise stated, structures depicted herein are also meant to include compounds which differ only in the presence of one or more isotopically enriched atoms. For 0 example, compounds having the present structures except for the replacement of a hydrogen by a deuterium or tritium, or the replacement of a carbon by I 3 C- or 4 C-enriched carbon are within the scope of this invention. [0056] The compounds of the present invention may also contain unnatural proportions of atomic isotopes at one or more of atoms that constitute such compounds. For example, the 5 compounds may be radiolabeled with radioactive isotopes, such as for example tritium (H), iodine-125 (125I) or carbon-14 ( 14 C). All isotopic variations of the compounds of the present invention, whether radioactive or not, are encompassed within the scope of the present invention. [0057] The term "pharmaceutically acceptable salts" is meant to include salts of active 3 compounds which are prepared with relatively nontoxic acids or bases, depending on the particular substituent moieties found on the compounds described herein. When compounds of the present invention contain relatively acidic functionalities, base addition salts can be obtained by contacting the neutral form of such compounds with a sufficient amount of the desired base, either neat or in a suitable inert solvent. Examples of pharmaceutically 5 acceptable base addition salts include sodium, potassium, calcium, ammonium, organic amino, or magnesium salt, or a similar salt. When compounds of the present invention contain relatively basic functionalities, acid addition salts can be obtained by contacting the neutral form of such compounds with a sufficient amount of the desired acid, either neat or in a suitable inert solvent. Examples of pharmaceutically acceptable acid addition salts include 0 those derived from inorganic acids like hydrochloric, hydrobromic, nitric, carbonic, monohydrogencarbonic, phosphoric, monohydrogenphosphoric, dihydrogenphosphoric, sulfuric, monohydrogensulfuric, hydriodic, or phosphorous acids and the like, as well as the 12 WO 2007/114926 PCT/US2007/008395 salts derived from relatively nontoxic organic acids like acetic, propionic, isobutyric, maleic, malonic, benzoic, succinic, suberic, fumaric, lactic, mandelic, phthalic, benzenesulfonic, p tolylsulfonic, citric, tartaric, methanesulfonic, and the like. Also included are salts of amino acids such as arginate and the like, and salts of organic acids like glucuronic or galactunoric 5 acids and the like (see, for example, Berge et al., "Pharmaceutical Salts", Journal of Pharmaceutical Science, 1977, 66, 1-19). Certain specific compounds of the present invention contain both basic and acidic functionalities that allow the compounds to be converted into either base or acid addition salts. [00581 In addition to salt forms, the present invention provides compounds, which are in a 0 prodrug form. Prodrugs of the compounds described herein are those compounds that readily undergo chemical changes under physiological conditions to provide the compounds of the present invention. Additionally, prodrugs can be converted to the compounds of the present invention by chemical or biochemical methods in an ex vivo environment. For example, prodrugs can be slowly converted to the compounds of the present invention when placed in a 5 transdermal patch reservoir with a suitable enzyme or chemical reagent. [00591 The terms "a,""an," or "a(n)", when used in reference to a group of substituents herein, mean at least one. For example, where a compound is substituted with "an" alkyl or aryl, the compound is optionally substituted with at least one alkyl and/or at least one aryl. Moreover, where a moiety is substituted with an R substituent, the group may be referred to .0 as "R-substituted." Where a moiety is R-substituted, the moiety is substituted with at least one R substituent and each R substituent is optionally different. [00601 Description of compounds of the present invention are limited by principles of chemical bonding known to those skilled in the art. Accordingly, where a group may be substituted by one or more of a number of substituents, such substitutions are selected so as 25 to comply with principles of chemical bonding and to give compounds which are not inherently unstable and/or would be known to one of ordinary skill in the art as likely to be unstable under ambient conditions, such as aqueous, neutral, and several known physiological conditions. For example, a heterocycloalkyl or heteroaryl is attached to the remainder of the molecule via a ring heteroatom in compliance with principles of chemical bonding known to 30 those skilled in the art thereby avoiding inherently unstable compounds. [00611 The terms "treating" or "treatment" refers to any indicia of success in the treatment or amelioration of an injury, pathology or condition, including any objective or subjective 13 WO 2007/114926 PCT/US2007/008395 parameter such as abatement; remission; diminishing of symptoms or making the injury, pathology or condition more tolerable to the patient; slowing in the rate of degeneration or decline; making the final point of degeneration less debilitating; improving a patient's physical or mental well-being. The treatment or amelioration of symptoms can be based on 5 objective or subjective parameters; including the results of a physical examination, neuropsychiatric exams, and/or a psychiatric evaluation. For example, the certain methods presented herein successfully treat cancer by decreasing the incidence of cancer and or causing remission of cancer. [00621 An "effective amount" is an amount sufficient to contribute to the treatment, 0 prevention, or reduction of a symptom or symptoms of a disease. An "effective amount" may also be referred to as a "therapeutically effective amount." A "reduction" of a symptom or symptoms (and grammatical equivalents of this phrase) means decreasing of the severity or frequency of the symptom(s), or elimination of the symptom(s). A "prophylactically effective amount" of a drug is an amount of a drug that, when administered to a subject, will 5 have the intended prophylactic effect, e.g., preventing or delaying the onset (or reoccurrence) a disease, or reducing the likelihood of the onset (or reoccurrence) of a disease or its symptoms. The full prophylactic effect does not necessarily occur by administration of one dose, and may occur only after administration of a series of doses. Thus, a prophylactically effective amount may be administered in one or more administrations. An "activity 0 decreasing amount," as used herein, refers to an amount of antagonist required to decrease the activity of an enzymne relateive'to the absence of the antagonist. A "function disrupting amount," as used herein, refers to the amount of antagonist required to disrupt the function of an osteoclast or leukocyte relative to the absence of the antagonist. [00631 As used herein, the "antagonist" or "the compound of the present invention" refers 25 to a compound of Formula (I), or a P13-Kinase affinity pocket binding antagonist (e.g. a P13 Kinase affinity pocket binding pyrazolopyrimidine antagonists, or a P13-Kinase affinity pocket binding pyrrolopyrimidine antagonist). A "compound of Formula (I)" includes the compounds of Formulae (I)-(X) as described below. II. Kinase Antagonists 30 [00641 In one aspect, the present invention provides novel kinase antagonists. The kinase antagonists may be a P13-Kinase affinity pocket binding antagonist (e.g. a P13-Kinase affinity 14 WO 2007/114926 PCT/US2007/008395 pocket binding pyrazolopyrimidine antagonist, or P13-Kinase affinity pocket binding pyrrolopyrimidine antagonist) or a compound of Formula (I). The P13-Kinase affinity pocket binding antagonists of the present invention are compounds containing a P13-Kinase affinity pocket binding moiety. The PI3-Kinase affinity pocket binding pyrazolopyrimidine 5 antagonists of the present invention are substituted pyrazolopyrimidine compounds containing a PI3-Kinase affinity pocket binding moiety. Likewise, the P13-Kinase affinity pocket binding pyrrolopyrimidine antagonists of the present invention are substituted pyrrolopyrimidine compounds containing a P13-Kinase affinity pocket binding moiety. [0065] The P13-Kinase affinity pocket binding moiety is a substituent which, upon D contacting a p11 Oc, p110P, p1 Oy, or p1108 kinase, fills space within the corresponding P13 Kinase affinity pocket. In some embodiments, the P13-Kinase affinity pocket binding moiety displaces at least one water molecule within the P13-Kinase affinity pocket. The P13-Kinase affinity pocket binding moiety may also interact with one or more amino acids that from part of the P13-Kinase affinity pocket. A description of the P13-Kinase affinity pocket and 5 methods of determining whether a substituent fills space within the P13-Kinase affinity pocket are set forth below. [0066] In some embodiments, the kinase antagonist of the present invention has the formula:

R

36

R

2 N~' N N Ri (I) 20 In Formula (I), R' is hydrogen, halogen, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.

R

2 is halogen, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, 25 substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl. X is =N- or =C(H)-. R36 is halogen, -NR R, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl. 15 WO 2007/114926 PCT/US2007/008395

R

37 and R 38 are independently hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl. In some embodiments, R 37 and R 3 8 are independently hydrogen, or unsubstituted alkyl. R 2 5 may be a P13-Kinase affinity pocket binding moiety. [00671 In some embodiments, R 36 is -NH2. Thus, the kinase antagonist may have the formula:

NH

2

R

2 NX N N RI (II). [0068] In some embodiments, R', R 2 , and X are as defined above in Formula (I). In certain 0 embodiments, X is =N-. [00691 In some embodiments. of Formulae (I) and (II), R 1 is hydrogen, R 3 -substituted or unsubstituted alkyl, R 3 -substituted or unsubstituted heteroalkyl, R 3 -substituted or unsubstituted cycloalkyl, R 3 -substituted or unsubstituted heterocycloalkyl, R 3 -substituted or unsubstituted aryl, or R 3 -substituted or unsubstituted heteroaryl. R 2 is halogen, R 4 -substituted 5 aryl, or substituted or unsubstituted heteroaryl; [00701 R 3 is halogen, -CN, -OR, -S(O),R 6 , -NRR 8 , -C(O)R 9 , =N-NH 2 , -NR 1 I-C(O)R",

-NR

2 -C(O)-ORD , -C(O)NR 1 4

RI

5 , -NR 16

S(O)

2 R', -S(O) 2

NR

1 ", R' 9 -substituted or unsubstituted alkyl, R' 9 -substituted or unsubstituted heteroalkyl, R' 9 -substituted or unsubstituted cycloalkyl, R 19 -substituted or unsubstituted heterocycloalkyl, R 19 -substituted or 0 unsubstituted aryl, or R' 9 -substituted or unsubstituted heteroaryl. Then symbol n is an integer from 0 to 2. [0071] R 4 is halogen, -CN, -OR 2 0 , -S(O)qR, -NR 2

R

23 , -C(O)R 2 4 , =N-NH 2 , -NR 2 5 _

C(O)R

26 , -NR 27

-C(O)-OR

2 8 , -C(O)NR 2 9

R

3 0 , -NR? 1

S(O)

2

R

32 , -S(O) 2 NRe, R 34 -substituted or unsubstituted alkyl, R 34 -substituted or unsubstituted heteroalkyl, R 34 -substituted or 5 unsubstituted cycloalkyl, R 34 -substituted or unsubstituted heterocycloalkyl, R 34 -substituted or unsubstituted aryl, or R 34 -substituted or unsubstituted heteroaryl. The symbol q represents an integer from 0 to 2. 16 WO 2007/114926 PCT/US2007/008395 [00721 R, R , R , R% R?, R O, R , R , R , R 14, R ", R 16 , R 17 , R 18 , R 2 0 , R, R 2 , R 3 , R 2 4 ,

R

25 , R, R, R8, R29, R 30 , R, R 2 , and R 3 are independently hydrogen, R 35 -substituted or unsubstituted alkyl, R3 5 -substituted or unsubstituted heteroalkyl, unsubstituted cycloalkyl,

R

3 5 -substituted or unsubstituted heterocycloalkyl, R 3 5 -substituted or unsubstituted aryl, or 5 R 5 -substituted or unsubstituted heteroaryl. R' 9 , R 34 and R 35 are independently hydrogen, halogen, unsubstituted alkyl, unsubstituted heteroalkyl, unsubstituted cycloalkyl, unsubstituted heterocycloalkyl, unsubstituted aryl, or unsubstituted heteroaryl. [00731 In some embodiments, R 5 , R 6 , R 7 , R, R 9 , R 10 , Ru, R"1, R, 1 3

R

1 4 , R 15 , R 1 6 , R 17 , R1 8 , R20, R 21 , R , R 2 3 , R 24 , Rs, R26, R, Rs, R9, R 30 , R, R 2 , and R 3 are independently 0 hydrogen, unsubstituted alkyl, unsubstituted heteroalkyl, unsubstituted cycloalkyl, unsubstituted heterocycloalkyl, unsubstituted aryl, or unsubstituted heteroaryl. R 2 , R, R, RM, R24, R , R26, R2, R s, R29, R 30 , R 1 , R 2 , and R? 3 may independently be hydrogen, unsubstituted alkyl, or unsubstituted heteroalkyl. [00741 R' may be R 3 -substituted or unsubstituted alkyl, R-substituted or unsubstituted 5 cycloalkyl, or R 3 -substituted or unsubstituted aryl. R' may also be R 3 -substituted or unsubstituted alkyl, or R 3 -substituted or unsubstituted cycloalkyl. In some embodiments, R' is R-substituted or unsubstituted C1-C 4 alkyl, or Ra-substituted or unsubstituted C 3

-C

6 cycloalkyl. In other embodiments, R 1 is R-substituted or unsubstituted C 1

-C

4 alkyl, or R3_ substituted or unsubstituted cyclopentyl. R 1 may also be methyl or unsubstituted C 3

-C

6 0 branched alkyl (e.g. isopropyl, isobutyl, etc.). [0075] In certain embodiments, R 3 is R1 9 -substituted or unsubstituted alkyl, R' 9 -substituted or unsubstituted cycloalkyl, or R 19 -substituted or unsubstituted aryl. R 3 may also be R1 9 substituted or unsubstituted alkyl, R1 9 -substituted or unsubstituted cycloalkyl, or R19 substituted or unsubstituted aryl. In some embodiments, R 3 is R 19 -substituted or .5 unsubstituted alkyl, or R1 9 -substituted or unsubstituted cycloalkyl. 100761 R 19 may be unsubstituted alkyl or unsubstituted cycloalkyl. In come embodiments, R1 9 is unsubstituted C-C 4 alkyl or unsubstituted cyclopentyl. [00771 In some embodiments, R 2 is R 4 -substituted aryl, or R 4 -substituted or unsubstituted heteroaryl. R 2 may be R 4 -substituted phenyl, R 4 -substituted or unsubstituted naphthyl, R 4 0 substituted or unsubstituted pyridinyl, R 4 -substituted or unsubstituted pyrimidinyl, R 4 substituted or unsubstituted thiophenyl, R 4 -substituted or unsubstituted furanyl, R 4 17 WO 2007/114926 PCT/US2007/008395 substituted or unsubstituted indolyl, R 4 -substituted or unsubstituted benzoxadiazolyl, R 4 substituted or unsubstituted benzodioxolyl, R 4 -substituted or unsubstituted benzodioxanyl,

R

4 -substituted or unsubstituted thianaphthanyl, R 4 -substituted or unsubstituted pyrrolopyridinyl, R 4 -substituted or unsubstituted indazolyl, R 4 -substituted or unsubstituted 5 tetrahydronaphthalenyl, R 4 -substituted or unsubstituted quinolinyl, R 4 -substituted or unsubstituted quinoxalinyl, R 4 -substituted or unsubstituted pyridopyrazinyl, R 4 -substituted or unsubstituted quinazolinonyl, R 4 -substituted or unsubstituted chromenonyl, R 4 -substituted or unsubstituted benzoisoxazolyl, R 4 -substituted or unsubstituted imidazopyridinyl, R 4 substituted or unsubstituted benzofuranyl, R 4 -substituted or unsubstituted dihydro 0 benzofuranyl, R 4 -substituted or unsubstituted dihydro-benzodioxinyl, R 4 -substituted or unsubstituted benzoimidazolonyl, or RI-substituted or unsubstituted benzothiophenyl. [0078] In certain embodiments, R 2 is R 4 -substituted phenyl, R 4 -substituted or unsubstituted pyrrolepyridinyl, R 4 -substituted or unsubstituted quinolinyl, R 4 -substituted or unsubstituted indazolyl, R 4 -substituted or unsubstituted quinolinyl indolyl, or R 4 -substituted or 5 unsubstituted naphthyl. R 4 may be halogen, -CN, -OR 20 , or -NR 2

R

3 . R 4 may also simply be halogen, or -OR 2 0 . [0079] In certain embodiments, R2 is has the formula: W1 ( 4 In Formula (III), WI, W 2 , W 3 , and W 4 are independently =CH-, =CR 4 -, or =N-. Each R 4 is as 20 defined above in the description of Formulae (I) and (II). Ring A is a substituted or unsubstituted heteroaryl or substituted or unsubstituted heterocycloalkyl. In some embodiments, ring A is a 6 to 7 membered heterocycloalkyl or 6 to 7 membered heteroaryl. Thus, in some embodiments, ring A is partially or fully unsaturated 6- or 7- membered ring. [00801 R 20 may be hydrogen or unsubstituted C 1

-C

10 alkyl. In some embodiments, R 2 0 is 25 hydrogen or unsubstituted C 1

-C

4 alkyl. R 2 0 may also simply be hydrogen or methyl. [00811 In some embodiments, R 2 has the formula: 18 WO 2007/114926 PCT/US2007/008395 OH OH \/OH (IV), R 4 (V), or R 4 (VI). In Formulae (IV), (V) and (VI), R is absent, halogen, unsubstituted C -C 4 alkyl, or -OR 2 0 . The halogen may be F, Cl, or Br. In some embodiments, the halogen is F or Cl. In other embodiments, the halogen is F. R 2 0 may be hydrogen or unsubstituted C-C 4 alkyl. 5 [0082] In some embodiments, R 2 is 6-hydroxynaphthyl, unsubstituted 7-azaindole, unsubstituted indolyl, unsubstituted indazolyl, or unsubstituted quinolinyl. [00831 In some embodiments, R 2 has the formula: 0OR2) z OR0) (VII) or Z (VIWil) In Formulae (VII) and (VIII), R 2 0 is as defined above. It is noted that, in accordance with the 0 description of R 2 0 above, each R 20 is optionally different. The symbol z is an integer from 1 to 5 (e.g. 1 or 2). In some embodiments, R 20 is hydrogen or unsubstituted C-CIO alkyl (e.g.

C,-C

5 alkyl such as methyl or ethyl). [00841 In some embodiments, R 2 has the formula: ORz OR 2 0 (IX), or (X). 15 In Formulae (IX) and (X), above, R 2 0 is as defined above, for example, in the description of Formulae (I), (II), (VI), and (VII) above. [00851 In some embodiments, each substituted group described above for the compounds of the present invention is substituted with at least one substituent group. More specifically, in some embodiments, each substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, 20 substituted heterocycloalkyl, substituted aryl, substituted heteroaryl, aryl(C-C 6 )alkyl, and heteroaryl(CI-C 6 )alkyl described above is substituted with at least one substituent group. In other embodiments, at least one or all of these groups are substituted with at least one size limited substituent group. Alternatively, at least one or all of these groups are substituted with at least one lower substituent group. 19 WO 2007/114926 PCT/US2007/008395 [00861 In other embodiments of the compounds described above, each substituted or unsubstituted alkyl is a substituted or unsubstituted C 1

-C

20 alkyl, each substituted or unsubstituted heteroalkyl is a substituted or unsubstituted 2 to 20 membered heteroalkyl, each substituted or unsubstituted cycloalkyl is a substituted or unsubstituted C 4

-C

8 cycloalkyl, each 5 substituted or unsubstituted heterocycloalkyl is a substituted or unsubstituted 4 to 8 membered heterocycloalkyl. [0087] Alternatively, each substituted or unsubstituted alkyl is a substituted or unsubstituted Ci-C 8 alkyl, each substituted or unsubstituted heteroalkyl is a substituted or unsubstituted 2 to 8 membered heteroalkyl, each substituted or unsubstituted cycloalkyl is a 0 substituted or unsubstituted C 5 -C7 cycloalkyl, and each substituted or unsubstituted heterocycloalkyl is a substituted or unsubstituted 5 to 7 membered heterocycloalkyl. [0088] In another embodiment, the compounds of Formula (I) include any or all of the compounds listed in Table 1 below. III. The P13-Kinase Affinity Pocket 5 [0089] The term "P13-Kinase affinity pocket," as used herein, refers to a cavity within p11 Oct, p1 100, p1 Oy, and p1108 corresponding to the lightly shaded region shown in Figures 2A, 2C, and 2D labeled "Affinity Pocket." Figures 2A, 2C, and 2D illustrate a computer model of the p110y crystal structure. In p1 10y, the surface of the P13-Kinase affinity pocket is bound, at least in part, by the side chain of K833, D964, 1879, and D841 (p1 10y 20 numbering, see Figure 8). The surface of the corresponding cavity in p1108 is bound, at least in part, by the side chain of K779, D911, 1825, and D787 (p1108 numbering, see Figure 7). The corresponding cavity within p110Iia is bound, at least in part, by the side chains of K802, D933, 1848, and D810 (p11 Oct numbering, see Figure 9). The corresponding cavity within p110p is bound, at least in part, by the side chains of K805, D937, 1851, and D813 (p110p 25 numbering, see Figure 10). The PI3-Kinase affinity pocket is not accessed by ATP. [00901 The P13-Kinase affinity pocket of p1108 may be referred to herein as the p1106 affinity pocket. Likewise, the PI3-Kinase affinity pocket of p1l 0 y may be referred to herein as the p1 lOy affinity pocket. The P13-Kinase affinity pocket includes lysine 779, which, according to computer models, forms a hydrogen bond with the pyridine nitrogen of PIK-90 30 and the phenol oxygen of PI 103 (Figure 2D), both of which are inhibitors of p 1108. Based 20 WO 2007/114926 PCT/US2007/008395 on these computer modeling results, a novel antagonist was designed based on the chemical structure of PIK-39 and IC87114, as detailed below. [00911 As shown in Figure 2C, PIK-39 does not contain a P13-Kinase binding pocket moiety. And as shown in Figure 3A, IC87114 maintains contacts to E880 and V882 in the 5 ATP binding region of p1108, but is also missing a PI3-Kinase binding pocket moiety. By inserting m-phenol (a P13-Kinase binding pocket moiety) at the C3 of the pyrazolopyrimidine . of IC87114, the P13-Kinase affinity pocket is accessed (FIG. 3A) resulting in a 60-fold increase in p1108 inhibition potency. [00921 As described above, a PI3-Kinase binding pocket moiety is a substituent which, 0 upon contacting upon contacting pl10a, p11OP, p1 10y, or p1108, fills space within the corresponding P13-Kinase binding pocket. For example, a P13-Kinase affinity pocket binding moiety is a substituent which, upon contacting upon contacting p1105, fills space within the . p110c affinity pocket. Likewise, a p110o affinity pocket binding moiety is a substituent which, upon contacting upon contacting p11 Oa, fills space within the p11Oa affinity pocket. 5 [0093] In some embodiments, the P13-Kinase binding pocket moiety additionally interacts (e.g. bonds) with an amino acid that forms part of the P13-Kinase binding pocket. In some related embodiments, the interaction is a hydrogen bond, van der Waals interaction, ionic bond, covalent bond (e.g. disulfide bond) or hydrophobic interaction. IV. Determining Space Filling Within the P13-Kinase Affinity Pocket 20 [00941 To determine whether the PI3-Kinase affinity pocket binding moiety fills space within the P13-Kinase affinity pocket, computer modeling techniques are employed. A query PI3-Kinase affinity pocket binding antagonist (i.e. a test compound) is fit into a computer image ofpll0y. The p110y computer image is derived from the solved co-crystal structure of human p1lOy bound to PIK-39. The PyMOL Molecular Graphics System may be employed 25 to generate the image. An example is presented in Figure 3A, wherein IC87114 and PIK-294 are built into the computer image of p 11Oy kinase, derived from the p 11 Oy - PIK-39 co crystal. See Knight, et al., Cell 125: 733-745 (2006). [00951 The computer models are typically analyzed to prevent any gross steric clashes and to satisfy key hydrogen bonds between the query PI3-Kinase affinity pocket binding 30 antagonist and the p1 1 0 y protein (e.g. V882 and M804). In some embodiments, energy 21 WO 2007/114926 PCT/US2007/008395 minimization calculations are performed to optimize binding energy. Using these techniques, one skilled in the art can easily determine whether a query P13-Kinase affinity pocket binding antagonist includes a P13-Kinase affinity pocket binding moiety that fills space within the PI3-Kinase affinity pocket. 5 [00961 In some embodiments, the query P13-Kinase affinity pocket binding antagonist is analyzed to determine whether at least one bond (e.g. a hydrogen bond) is formed between the query P13-Kinase affinity pocket binding antagonist and an amino acid that form part of the P13-Kinase affinity pocket. Using a computer modeling technique as described above, the distance between one or more amino acids that form part of the P13-Kinase affinity D pocket and a potential contact point on the P13-Kinase affinity pocket binding moiety is determined. Based on this distance, one skilled in the art may determine whether at least one bond is formed between one or more amino acids that form part of the P13-Kinase affinity pocket and a P13-Kinase affinity pocket binding moiety. V. General Syntheses 5 [0097] The compounds of the invention are synthesized by an appropriate combination of generally well known synthetic methods. Techniques useful in synthesizing the compounds of the invention are both readily apparent and accessible to those of skill in the relevant art. The discussion below is offered to illustrate certain of the diverse methods available for use in assembling the compounds of the invention. However, the'discussion is not intended to D define the scope of reactions or reaction sequences that are useful in preparing the compounds of the present invention. Scheme I R2

NH

2

NH

2 I NH 2 I - 'H NH 2

R

2 X -- N Br-R B(H)N N N. N_ N 2LL N N N N H H N [00981 In Scheme I above, iodination of the pyrazolo- or pyrrolo-pyrimidine is 5 accomplished using an appropriate iodinatioi reagent, such as n-iodo-succinamide. Elaboration of the 1-position may be accomplished via halogen displacement of a brominated substituent (e.g. a substituted or unsubstituted alkylbromide). Palladium-catalyzed cross coupling between organoboronic acid and the iodo halide (i.e. Suzuki coupling), is then used 22 WO 2007/114926 PCT/US2007/008395 to elaborate the 3-position. Recent catalyst and method developments have broadened the possible Suzuki coupling applications enormously, so that the scope of the reaction partners is not restricted to aryls. Potassium trifluoroborates and organoboranes or boronate esters may be used in place of boronic acids. Some pseudohalides (for example triflates) may also 5 be used as coupling partners. Further information regarding Suzuki coupling may be found, for example in Kudo et al., Angew. Chem. Int. Ed. 45: 1282-1284 (2006); Kirchhoffet al., J. Am. Chem. Soc., 124: 13662-13663 (2002); Wu et al., J. Org. Chem., 68: 670-673 (2003); and Molander et al., J. Org. Chem., 67: 8424-8429 (2002). VI. Methods 0 [0099] In another aspect, the present invention provides methods of decreasing the catalytic activity of a P13 Kinase (e.g. ap1 10c kinase). The method includes the step of contacting the P13 kinase with an activity decreasing amount of a compound of the present invention (i.e. a P13-Kinase affinity pocket binding antagonist or the compound of Formula (I)). In some embodiments, the antagonist is capable of decreasing the catalytic activity of a tyrosine 5 kinase. In some embodiments, the antagonist is a P13-Kinase affinity pocket binding pyrazolopyrimidine antagonists, or P13-Kinase affinity pocket binding pyrrolopyrimidine antagonists. [01001 In some embodiments, the antagonist is specific to plOcx relative to the antagonist action against p1105, p1 10p, and/or p1 10y. In some embodiments, the IC50 for pl10a is at .0 least 1.5, 2.0, 3.0, 4.0, 5.0, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 200, 500, or 1000 fold lower than the IC50 against p1108, p 1 1 lp, and/or p1 10y. In other embodiments, the IC50 of the antagonist against the p11Oot is less than 100 pM, 50 pM, 40 PM, 30 pM, 20 PM, 10 pM, 5 pM, 1 pM, 0.5 pM, 0.1 pM, 50 nM, 10 nM, 1 nM. 0.5 nM, 0.1 nM, 50 pM, 10 pM, or I pM. 25 [0101] In some embodiments, the antagonist is specific to p1lOa relative to the antagonist action against insulin receptor tyrosine kinase. In some embodiments, the IC50 for plOa is at least 1.5, 2.0, 3.0, 4.0, 5.0, 10, 20, 30,40, 50, 60, 70, 80, 90, 100, 200, 500, or 1000 fold lower than the IC50 against insulin receptor tyrosine kinase. In other embodiments, the IC50 of the antagonist against the p110a is less than 100 pM, 50 pM, 40 pM, 30 PM, 20 pM, 10 30 pM, 5 pM, 1 pM, 0.5 pM, 0.1 pM, 50 nM, lOnM, 1 nM. 0.5 nM, 0.1 nM, 50 pM, 10pM, or 1 pM. 23 WO 2007/114926 PCT/US2007/008395 [01021 In some embodiments, the antagonist decreases, or is capable of decreasing, the catalytic activity of a tyrosine kinase. In some embodiments, the IC50 of the antagonist against the tyrosine kinase is less than 100 pM, 50 pM, 40 pM, 30 p.M, 20 pM, 10 pM, 5 pM, 1 pM, 0.5 pM, 0.1 p.M, 50 nM, 10 nM, 1 nM. 0.5 nM, 0.1 nM, 50 pM, 10 pM, or I pM. 5 Some tyrosine kinases include, for example, DNA-dependent protein kinase DNA-dependent protein kinase (pubmed protein accession number (PPAN) AAA79184), Abl tyrosine kinase (CAA52387), Bcr-Abl, hemopoietic cell kinase (PPAN CAI19695), Src (PPAN CAA24495), vascular endothelial growth factor receptor 2 (PPAN ABB82619), vascular endothelial growth factor receptor-2 (PPAN ABB82619), epidermal growth factor receptor (PPAN 0 AG43241), EPH receptor B4 (PPAN EAL23820), stem cell factor receptor (PPAN AAF22141), Tyrosine-protein kinase receptor TIE-2 (PPAN Q02858), fins-related tyrosine kinase 3 (PPAN NP_004110), platelet-derived growth factor receptor alpha (PPAN NP_990080), RET (PPAN CAA73131), and functional mutants thereof. In some embodiments, the tyrosine kinase is Abl, Bcr-Abl, EGFR, or Flt-3. 5 [01031 In some embodiments, the antagonist decreases, or is capable of decreasing, the catalytic activity of mTOR (PPAN AA117167). In some embodiments, the IC50 of the antagonist against mTOR is less than 100 [tM, 50 jiM, 40 PM, 30 piM, 20 pM, 10 pM, 5 pM, 1 pM, 0.5 pM, 0.1 pM, 50 nM, 10 nM, 1 nM. 0.5 nM, 0.1 nM, 50 pM, 10 pM, or 1 pM. [0104] In some embodiments, the antagonist decreases, or is capable of decreasing, the 0 catalytic activity of mTOR and p1 10c at an IC50 of less than 100 pM, 50 pM, 40 pM, 30 p.M, 20 pM, 10 pM, 5 pM, 1 pM, 0.5 pM, 0.1 pM, 50 rM, 10 riM, 1 nM. 0.5 nM, 0.1 nM, 50 pM, 10 pM, or 1 pM. In other embodiments, the antagonist decreases, or is capable of decreasing, the catalytic activity of a tyrosine kinase and p110ax at an IC50 of less than 100 pM, 50 pM, 40 ttM, 30 pM, 20 pM, 10 pM, 5 pM, 1 pM, 0.5 pM, 0.1 pM, 50 nM, 10 nM, 1 Z5 nM. 0.5 nM, 0.1 nM, 50 pM, 10 pM, or 1 pM. In other embodiments, the antagonist decreases, or is capable of decreasing, the catalytic activity of a tyrosine kinase, mTOR, and p110 c at an IC50 of less than 100 pM, 50 pM, 40 pM, 30 pM, 20 pM, 10 pM, 5 pM, 1 jiM, 0.5 pM, 0.1 M, 50 nM, 10 nM, 1 nM. 0.5 nM, 0.1 nM, 50 pM, 10 pM, or 1 pM. [0105] In another aspect, the present invention provides a method of treating a disease or 0 condition mediated by P13 kinase activity, PI3 Kinase activity and Tyrosine Kinase Activity, P13 Kinase activity and mTOR Activity, or PI3 Kinase activity, mTOR activity, and Tyrosine 24 WO 2007/114926 PCT/US2007/008395 Kinase Activity in a subject in need of such treatment. The method includes administering to the subject a therapeutically effective amount of an antagonist. The antagonist is a P13 Kinase affinity pocket binding antagonist or the compound of Formula (I). In some embodiments the antagonist is a P13-Kinase affinity pocket binding pyrazolopyrimidine 5 antagonists, or P13-Kinase affinity pocket binding pyrrolopyrimidine antagonists. [0106] The disease may also be a bone-resorption disorder, chronic myelogenous leukemia, abnormal inflammation, autoimmune disease, thrombosis, or asthma. The disease may also be a type of cancer or cancer metastasis, including, for example, leukemia, carcinomas and sarcomas, such as cancer of the brain, breast, cervix, colon, head & neck, liver, kidney, lung, 0 non-small cell lung, melanoma, mesothelioma, ovary, sarcoma, stomach, uterus and Medulloblastoma. Additional examples include, Hodgkin's Disease, Non-Hodgkin's Lymphoma, multiple myeloma, neuroblastoma, ovarian cancer, rhabdomyosarcoma, primary thrombocytosis, primary macroglobulinemia, primary brain tumors, cancer, malignant pancreatic insulanoma, malignant carcinoid, urinary bladder cancer, premalignant skin 5 lesions, testicular cancer, lymphomas, thyroid cancer, neuroblastoma, esophageal cancer, genitourinary tract cancer, malignant hypercalcemia, endometrial cancer, adrenal cortical cancer, neoplasms of the endocrine and exocrine pancreas, and prostate cancer. In some embodiments, the disease is selected from disease is liver cancer, colon cancer, breast cancer, melanoma, acute myelogenous leukemia, chronic myelogenous leukemia, or nonsmall-cell O lung cancer. [01071 In another aspect, the present invention provides methods of disrupting the function of a leukocyte or disrupting a function of an osteoclast. The method includes contacting the leukocyte or the osteoclast with a function disrupting amount of the antagonist. The antagonist is a PI3-Kinase affinity pocket binding antagonist or the compound of Formula (I). 25 In some embodiments the antagonist is a PI3-Kinase affinity pocket binding pyrazolopyrimidine antagonist, or P13-Kinase affinity pocket binding pyrrolopyrimidine antagonist. VI. Pharmaceutical Formulations [0108] In another aspect, the present invention provides a pharmaceutical composition 30 including an antagonist in admixture with a pharmaceutically acceptable excipient. One of skill in the art will recognize that the pharmaceutical compositions include the 25 WO 2007/114926 PCT/US2007/008395 pharmaceutically acceptable salts of the P13-Kinase antagonists of the present invention described above. [0109] In therapeutic and/or diagnostic applications, the compounds of the invention can be formulated for a variety of modes of administration, including systemic and topical or 5 localized administration. Techniques and formulations generally may be found in Remington: The Science and Practice of Pharmacy (20* ed.) Lippincott, Williams & Wilkins (2000). [0110] The compounds according to the invention are effective over a wide dosage range. For example, in the treatment of adult humans, dosages from 0.01 to 1000 mg, from 0.5 to 0 100 mg, from 1 to 50 mg per day, and from 5 to 40 mg per day are examples of dosages that may be used. A most preferable dosage is 10 to 30 mg per day. The exact dosage will depend upon the route of administration, the form in which the compound is administered, the subject to be treated, the body weight of the subject to be treated, and the preference and experience of the attending physician. 5 [0111] Pharmaceutically acceptable salts are generally well known to those of ordinary skill in the art, and may include, by way of example but not limitation, acetate, benzenesulfonate, besylate, benzoate, bicarbonate, bitartrate, bromide, calcium edetate, carnsylate, carbonate, citrate, edetate, edisylate, estolate, esylate, fumarate, gluceptate, gluconate, glutamate, glycollylarsanilate, hexylresorcinate, hydrabamine, hydrobromide, O hydrochloride, hydroxynaphthoate, iodide, isethionate, lactate, lactobionate, malate, maleate, mandelate, mesylate, mucate, napsylate, nitrate, pamoate (embonate), pantothenate, phosphate/diphosphate, polygalacturonate, salicylate, stearate, subacetate, succinate, sulfate, tannate, tartrate, or teoclate. Other pharmaceutically acceptable salts may be found in, for example, Remington: The Science and Practice of Pharmacy ( 2 0th ed.) Lippincott, Williams 25 & Wilkins (2000). Preferred pharmaceutically acceptable salts include, for example, acetate, benzoate, bromide, carbonate, citrate, gluconate, hydrobromide, hydrochloride, maleate, mesylate, napsylate, pamoate (embonate), phosphate, salicylate, succinate, sulfate, or tartrate. [01121 Depending on the specific conditions being treated, such agents maybe formulated into liquid or solid dosage forms and administered systemically or locally. The agents may 30 be delivered, for example, in a timed- or sustained- low release form as is known to those skilled in the art. Techniques for formulation and administration may be found in Remington: The Science and Practice of Pharmacy ( 2 0th ed.) Lippincott, Williams & Wilkins (2000). 26 WO 2007/114926 PCT/US2007/008395 Suitable routes may include oral, buccal, by inhalation spray, sublingual, rectal, transdermal, vaginal, transmucosal, nasal or intestinal administration; parenteral delivery, including intramuscular, subcutaneous, intramedullary injections, as well as intrathecal, direct intraventricular, intravenous, intra-articullar, intra -sternal, intra-synovial, intra-hepatic, 5 intralesional, intracranial, intraperitoneal, intranasal, or intraocular injections or other modes of delivery. [01131 For injection, the agents of the invention may be formulated and diluted in aqueous solutions, such as in physiologically compatible buffers such as Hank's solution, Ringer's solution, or physiological saline buffer. For such transmucosal administration, penetrants 3 appropriate to the barrier to be permeated are used in the formulation. Such penetrants are generally known in the art. [01141 Use of pharmaceutically acceptable inert carriers to formulate the compounds herein disclosed for the practice of the invention into dosages suitable for systemic administration is within the scope of the invention. With proper choice of carrier and suitable manufacturing 5 practice, the compositions of the present invention, in particular, those formulated as solutions, may be administered parenterally, such as by intravenous injection. The compounds can be formulated readily using pharmaceutically acceptable carriers well known in the art into dosages suitable for oral administration. Such carriers enable the compounds of the invention to be formulated as tablets, pills, capsules, liquids, gels, syrups, slurries, 3 suspensions and the like, for oral ingestion by a subject (e.g. patient) to be treated. [0115] For nasal or inhalation delivery, the agents of the invention may also be formulated by methods known to those of skill in the art, and may include, for example, but not limited to, examples of solubilizing, diluting, or dispersing substances such as, saline, preservatives, such as benzyl alcohol, absorption promoters, and fluorocarbons. 5 [0116] Pharmaceutical compositions suitable for use in the present invention include compositions wherein the active ingredients are contained in an effective amount to achieve its intended purpose. Determination of the effective amounts is well within the capability of those skilled in the art, especially in light of the detailed disclosure provided herein. [01171 In addition to the active ingredients, these pharmaceutical compositions may contain o suitable pharmaceutically acceptable carriers comprising excipients and auxiliaries which facilitate processing of the active compounds into preparations which can be used 27 WO 2007/114926 PCT/US2007/008395 pharmaceutically. The preparations formulated for oral administration may be in the form of tablets, dragees, capsules, or solutions. [0118] Pharmaceutical preparations for oral use can be obtained by combining the active compounds with solid excipients, optionally grinding a resulting mixture, and processing the 5 mixture of granules, after adding suitable auxiliaries, if desired, to obtain tablets or dragee cores. Suitable excipients are, in particular, fillers such as sugars, including lactose, sucrose, mannitol, or sorbitol; cellulose preparations, for example, maize starch, wheat starch, rice starch, potato starch, gelatin, gum tragacanth, methyl cellulose, hydroxypropylmethyl cellulose, sodium carboxymethyl-cellulose (CMC), and/or polyvinylpyrrolidone (PVP: 0 povidone). If desired, disintegrating agents may be added, such as the cross- linked polyvinylpyrrolidone, agar, or alginic acid or a salt thereof such as sodium alginate. [0119] Dragee cores are provided with suitable coatings. For this purpose, concentrated sugar solutions may be used, which may optionally contain gum arabic, talc, polyvinylpyrrolidone, carbopol gel, polyethylene glycol (PEG), and/or titanium dioxide, 5 lacquer solutions, and suitable organic solvents or solvent mixtures. Dye-stuffs or pigments may be added to the tablets or dragee coatings for identification or to characterize different combinations of active compound doses. [0120] Pharmaceutical preparations that can be used orally include push-fit capsules made of gelatin, as well as soft, sealed capsules made of gelatin, and a plasticizer, such as glycerol 0 or sorbitol. The push-fit capsules can contain the active ingredients in admixture with filler such as lactose, binders such as starches, and/or lubricants such as talc or magnesium stearate and, optionally, stabilizers. In soft capsules, the active compounds may be dissolved or suspended in suitable liquids, such as fatty oils, liquid paraffin, or liquid polyethylene glycols (PEGs). In addition, stabilizers may be added. 25 [0121] Depending upon the particular condition, or disease state, to be treated or prevented, additional therapeutic agents, which are normally administered to treat or prevent that condition, may be administered together with the inhibitors of this invention. For example, chemotherapeutic agents or other anti-proliferative agents may be combined with the inhibitors of this invention to treat proliferative diseases and cancer. Examples of known 30 chemotherapeutic agents include, but are not limited to, adriamycin, dexamethasone, vincristine, cyclophosphamide, fluorouracil, topotecan, taxol, interferons, and platinum derivatives. 28 WO 2007/114926 PCT/US2007/008395 [0122] Other examples of agents the inhibitors of this invention may also be combined with include, without limitation, anti-inflammatory agents such as corticosteroids, TNF blockers, IL-1 RA, azathioprine, cyclophosphamide, and sulfasalazine; immunomodulatory and immunosuppressive agents such as cyclosporin, tacrolimus, rapamycin, mycophenolate 5 mofetil, interferons, corticosteroids, cyclophophamide, azathioprine, and sulfasalazine; neurotrophic factors such as acetylcholinesterase inhibitors, MAO inhibitors, interferons, anti-convulsants, ion channel blockers, riluzole, and anti-Parkinsonian agents; agents for treating cardiovascular disease such as beta-blockers, ACE inhibitors, diuretics, nitrates, calcium channel blockers, and statins; agents for treating liver disease such as corticosteroids, 0 cholestyramine, interferons, and anti-viral agents; agents for treating blood disorders such as corticosteroids, anti-leukemic agents, and growth factors; agents for treating diabetes such as insulin, insulin analogues, alpha glucosidase inhibitors, biguanides, and insulin sensitizers; and agents for treating immunodeficiency disorders such as gamma globulin. [0123] These additional agents may be administered separately, as part of a multiple dosage 5 regimen, from the composition. Alternatively, these agents may be part of a single dosage form, mixed together with the inhibitor in a single composition. [0124] The present invention is not to be limited in scope by the exemplified embodiments, which are intended as illustrations of single aspects of the invention. Indeed, various modifications of the invention in addition to those described herein will become apparent to 0 those having skill in the art from the foregoing description. Such modifications are intended to fall within the scope of the invention. Moreover, any one or more features of any embodiment of the invention may be combined with any one or more other features of any other embodiment of the invention, without departing from the scope of the invention. For example, the P13-Kinase antagonists of the present invention described above are equally 25 applicable to the methods of treatment and methods of inhibiting kinases described herein. References cited throughout this application are examples of the level of skill in the art and are hereby incorporated by reference herein in their entirety for all purposes, whether previously specifically incorporated or not. VII. Examples 30 [01251 The following examples are meant to illustrate certain embodiments of the invention, and not to limit the scope of the invention. 29 WO 2007/114926 PCT/US2007/008395 101261 General Methods. All chemicals, reagents and solvents used were purchased commercially and used as received. dH2O refers to deioinized water. Evaporation of solvents was carried out on a rotary evaporator under reduced pressure. Compounds were purified by High Pressure Liquid Chromatography (HPLC) eluting with dH 2 0-MeCN 5 trifluroacetic acid, 50:50:0.1, unless otherwise indicated. Analysis of products was carried out on a Liquid Chromatography Mass Spectrometer (LCMS) using MeCN-0.1% formic acid (varying ratios) as eluent. A. Selected Reaction Procedures. [0127] Synthesis of IH-pyrazolo[3,4-d]pyrimidin-4-amine (BA18). A solution of 250 mL 3 of formamide and 3-amino-4-pyrazolecarbonitrile (25 g, 0.231 mol) was heated to 180*C overnight under an argon atmosphere. Reaction was cooled and 400 mL of dH 2 0 were added. The resulting solid was filtered and rinsed with cold dH 2 0. White solid precipitate was collected and dried in vacuo overnight to yield BA18 (39g, 100% yield). ESI-MS (M+H)* m/z calcd 136.1, found 136.1. 5 [01281 Synthesis of 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine (BA19). A solution of 3H-pyrazolo[3,4-d]pyrimidin-4-amine (1Og, 0.074 mol) and n-iodo-succinamide (25 g, 0.111 mol) in DMF (80 mL) was heated to 80*C overnight under an argon atmosphere. The resulting solid was filtered and rinsed with cold EtOH. Product was dried in vacua overnight to yield BA19 (24g, 100% yield). ESI-MS (M+H)* m/z calcd 262.0, found 262.0 .0 [01291 Synthesis of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (BA12). A solution of 3-iodo-lH-pyrazolo[3,4-d]pyrimidin-4-amine (2 g, 0.0077 mol) and K 2 C0 3 (4.2g, 0.031 mol) in DMIF (50 mL) was brought to 80*C under an argon atmosphere. Isopropylbromide (1.0g, 0.0084 mol) was added with a syringe. Reaction was refluxed under argon atmosphere for 2 hours. Solid K 2 C0 3 was removed by filtration. Solvent was partially .5 removed in vacuo. Sodium citrate (50 mL) was added and reaction was extracted with EtOAc. Organic phases concentrated in vacuo and purified using silica gel column chromatography [MeOH--CH 2 Cl 2 , 5:95] yielding BA12 (1.68 g, 72% yield). ESI-MS (M+H)* m/z called 304.0, found 304.1. [0130] General Suzuki coupling. Preparation of final products (see Table 1 for final 30 product names and structures). 30 WO 2007/114926 PCT/US2007/008395 [0131] 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (40 mg, 0.13 mmol, 1 equivalent) was dissolved in DME (12 ml). Boronic acid (1.1 equivalent) was dissolved in EtOH (3.3 ml) and added to reaction mixture. Pd(PPh3)4 (30 mg, 0.026 mmol, 0.2 equivalents) and saturated Na2CO3 (1.9 ml) were added to the reaction mixture and heated to 5 80*C under argon and refluxed for 8 hours. After cooling, the reaction was extracted with saturated NaCI and CH2C12. Organic phases were combined and solvent was removed. Resulting solid (or oil) was dissolved in dH20-MeCN-trifluroacetic acid, 50:50:0.1 and purified by HPLC. Purified product (varying yields) was confirmed by LCMS. [01321 Synthesis of 4-(4-Amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl) 0 benzenesulfonamide (BA14). A solution of benzenesulfonamide-4-boronic acid pinacol ester (23 mg, 0.08 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine (20 mg, 0.07 mmol) in DME (12 mL). Pd(PPh 3

)

4 (16 mg, 0.014 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere ovemight. After cooling, the reaction was extracted with 5 saturated NaCl and CH 2 Cl 2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA) to yield BA14 (2.2 mg, 10% yield). ESI-MS (M+H)* m/z calcd 333.1, found 333.1. [0133] Synthesis of 1-isopropyl-3-(3-methoxy-4-methylphenyl)-1H-pyrazolo[ 3

,

4 d]pyrimidin-4-amine (BA15). A solution of 2 methoxy-4-(4,4,5,5-tetramethyl-1,3-2 0 dioxaborolan-2-yl) phenol (19 mg, 0.08 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (20 mg, 0.07 mmol) in DME (12 mL). Pd(PPh 3

)

4 (16 mg, 0.014 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH 2 Cl 2 . Organic phases were combined, 25 concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA) to yield BA15 (4.3 mg, 20% yield). ESI-MS (M+H)* m/z calcd 300.1, found 300.2. [0134] Synthesis of 6-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)naphthalen 2-ol (BA17). A solution of 6-hydroxynaphthalen-2-yl-2-boronic acid (15 mg, 0.08 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin 30 4-amine (20 mg, 0.07 mmol) in DME (12 mL). Pd(PPh 3

)

4 (16 mg, 0.014 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and 31 WO 2007/114926 PCT/US2007/008395 CH2C12. Organic phases were combined, concentrated in vacuo and purified by RP-H{PLC (MeCN:H 2 0:0.1% TFA) to yield BA15 (4.8 mg, 23% yield). ESI-MS (M+H)* m/z caled 320.1, found 320.1. [01351 Synthesis of tert-butyl 4-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl) 5 2-methoxyphenylcarbamate (BA20). A solution of 4 4-N-Boc-amino-3-methoxy benzeneboronic acid (48 mg, 0.18 mmol) in EtOH (3.3 mL) was added to a solution of 3 iodo-1-isopropyl-lH-pyrazolo[3,4-d]pyrimidin-4-amine (50 mg, 0.18 mmol) in DME (12 mL). Pd(PPh 3

)

4 (40 mg, 0.03 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the 0 reaction was extracted with saturated NaCl and CH 2 0 2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA) to yield BA20. ESI-MS (M+H)* m/z calcd 399.2, found 399.1. [0136] Synthesis of 3-(4-amino-3-methoxyphenyl)-1-isopropyl-1H-pyrazolo[3,4 d]pyrimidin-4-aniine (BA20d). A solution of tert-butyl 4-(4-amino-1-isopropyl-lH 5 pyrazolo[3,4-d]pyrimidin-3-yl)-2-methoxyphenylcarbamate (BA20) (20 mg, 0.05 mmol) in

CH

2 0 2 , TFA, S(CH 2

)

2 , H20 (45:45:5:5) (lmL) was stirred at room temperature for 15 minutes. NaHCO 3 (2 mL) was added till reaction was alkaline. Reaction was extracted with H20 and CH 2 Cl 2 . Organic phases were combined, concentrated in vacuo and purified by RP HPLC (MeCN:H 2 0:0.1% TFA) to yield BA20d. D [01371 Synthesis of 5-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)pyridine-2 carbonitrile (BA21). A solution of 2-cyanopyridine 5-boronic acid pinocol ester (18 mg, 0.08 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-l-isopropyl-1H-pyrazolo[3,4 d]pyrimidin-4-amine (20 mg, 0.07 mmol) in DME (12 mL). Pd(PPh 3

)

4 (16 mg, 0.014 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an 5 argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH202. Organic phases were combined, concentrated in vacuo and purified by RP HPLC (MeCN:H 2 0:0.1% TFA) to yield BA21 (2.5 mg, 14% yield). ESI-MS (M+H)* m/z called 280.1, found 280.1. [0138] Synthesis of 3-(3-(benzyloxy)-5-fluorophenyl)-1-isopropyl-1H-pyrazolo[3,4 0 d]pyrimidin-4-amine.. A solution of (3-Benzyloxy-5-fluorophenyl)boronic acid (29 mg, 5.80 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-l-isopropyl-1H-pyrazolo[3,4 d]pyrimidin-4-amine (20 mg, 0.07 mmol) in DME (12 mL). Pd(PPh 3

)

4 (16 mg, 0.014 mnol) 32 WO 2007/114926 PCT/US2007/008395 and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH 2 Cl 2 . Organic phases were combined, concentrated in vacuo and purified by RP H{PLC (MeCN:H 2 0:0.1% TFA) to yield BA22 (15.6 mg, 60% yield). ESI-MS (M+H)* m/z calcd 378.1, found 378.0. [01391 Synthesis of 3-(4-amino-1-isopropyl-lH-pyrazolo[3,4-d]pyrimidin-3-yl)-5 fluorophenol (BA22). A solution of -(3-(benzyloxy)-5-fluorophenyl)-1-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine (15 mg, 0.04 mmol) in MeOH (0.9 mL) was flushed with argon. Pd on activated carbon (10 mL) was carefully added while keeping reaction under an ) argon atmosphere. Reaction was flushed with H 2 gas and left under H 2 atmosphere overnight at room temperature. The reaction was filtered through celite and rinsed with MeOH to yield BA22 (15 mg, 100% yield). ESI-MS (M+H)* m/z calcd 288.1, found 288.1. [0140] Synthesis of 1-isopropyl-3-(3,4-dimethoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4 amine (BA23). A solution of 3,4-Dimethoxyphenylboronic acid (24 mg, 0.13 mmol) in 5 EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin 4-amine (20 mg, 0.07 mmol) in DME (12 mL). Pd(PPh 3

)

4 (16 mg, 0.014 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80'C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and

CH

2 Cl 2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC D (MeCN:H 2 0:0.1% TFA) to yield BA23 (13.1 mg, 60% yield). ESI-MS (M+H)* m/z calcd 314.0, found 314.1. [0141] Synthesis of (3-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3 yl)phenyl)methanol (BA26). A solution of (3-Hydroxymethylphenyl)boronic acid (24 mg, 0.13 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-1H .5 pyrazolo[3,4-d]pyrimidin-4-amine (20 mg, 0.07 nimol) in DME (12 mL). Pd(PPh 3

)

4 (16mg, 0.0 14 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCI and CH 2 Cl 2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA) to yield BA26 (8.4 mg, 42% yield). ESI-MS 0 (M+H)* m/z calcd 283.1, found 284.2. [0142] Synthesis of 3-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-N-(4,5 dihydrothiazol-2-yl)benzamide (BA30). A solution of [3-((4,5-dihydrothiazol-2 33 WO 2007/114926 PCT/US2007/008395 yl)carbamoyl)phenyl]boronic acid (19 mg, 0.08 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-anine (20 mg, 0.07 mmol) in DME (12 mL). Pd(PPh 3

)

4 (16 mg, 0.014 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the 5 reaction was extracted with saturated NaC1 and CH 2 Cl 2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA) to yield BA30 (17.8 mg, 67% yield). [0143] Synthesis of 1-(4-(4-anino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3 yl)phenyl)ethanone (BA31). A solution of 4-Acetylphenylboronic acid (12.7 mg, 0.08 mmol) 0 in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4 d]pyrimidin-4-amine (20 mg, 0.07 mmol) in DME (12 mL). Pd(PPh 3

)

4 (16 mg, 0.014 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH 2

CI

2 . Organic phases were combined, concentrated in vacuo and purified by RP 5 HPLC (MeCN:H 2 0:0.1% TFA) to yield BA31 (12.9 mg, 62% yield). [01441 Synthesis of (3-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3 yl)phenyl)methanol (BA32). A solution of (4-Aminocarbonyl-3-chlorophenyl)boronic acid (16 mg, 0.08 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine (20 mg, 0.07 mmol) in DME (12 mL). Pd(PPh 3

)

4 (16 mg, 0 0.014 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH 2 Cl 2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA) to yield BA32 (9.7 mg, 42% yield). ESI-MS (M+H)* m/z calcd 331.1, found 331.1. 25 [0145] Synthesis of 5-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-3 methylthiophene-2-carbaldehyde (BA34). A solution of 5-Formiyl-3-methylthiophene-2 boronic acid (26 mg, 0.14 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1 isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (40 mg, 0.13 mmol) in DME (12 mL). Pd(PPh 3

)

4 (16 mg, 0.0 14 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction 30 was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH 2 Cl 2 . Organic phases were combined, concentrated in 34 WO 2007/114926 PCT/US2007/008395 vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA) to yield BA34 (14.7 mg, 38% yield). ESI-MS (M+H)* m/z calcd 302.1, found 302.0. [0146] Synthesis of 5-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)furan-3 carbaldehyde (BA35). A solution of 4-Formylfuran-2-boronic acid (20 mg, 0.14 mmol) in 5 EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin 4-amine (40 mg, 0.13 mmol) in DME (12 mL). Pd(PPh 3

)

4 (16 mg, 0.014 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and

CH

2

C

2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC 3 (MeCN:H 2 0:0.1% TFA) to yield BA35 (13.5 mg, 39% yield). ESI-MS (M+H)* m/z calcd 272.1, found 272.1. [0147] Synthesis of N-[3-(4-Amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl) phenyl]-methanesulfonamide (BA38). A solution of 3-Methanesulfonylaminophenylboronic acid (32 mg, 0.15 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl 5 1H-pyrazolo[3,4-d]pyrimidin-4-amine (40 mg, 0.13 mmol) in DME (12 mL). Pd(PPh 3

)

4 (16 mg, 0.014 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80'C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH 2 Cl 2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA) to yield BA38 (24.3 mg, 54% yield). ESI-MS 0 (M+H)* m/z calcd 347.1, found 347.0. [01481 Synthesis of 3-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)benzonitrile (BA39). A solution of 3-Cyanophenylboronic acid (23 mg, 0.15 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (40 mg, 0.13 mmol) in DME (12 mL). Pd(PPh 3

)

4 (30 mg, 0.03 mmol) and saturated Na 2

CO

3 (1.9 mL) 25 were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCI and CH 2 C1 2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA) to yield BA39 (14.9 mg, 41% yield). ESI-MS (M+H)* m/z calcd 279.1, found 279.0. [0149] Synthesis of N-[4-(4-Amino-l-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl) 30 phenyl]-methanesulfonamide (BA40). A solution of 4-Methanesulfonylaminophenylboronic acid (24 mg, 0.11 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl 1H-pyrazolo[3,4-d]pyrimidin-4-amine (30 mg, 0.10 nimol) in DME (12 mL). Pd(PPh) 4 (30 35 WO 2007/114926 PCT/US2007/008395 mg, 0.03 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH 2 Cl 2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA) to yield BA40 (0.9 mg, 3% yield). ESI-MS 5 (M+H)* m/z calcd 347.1, found 347.0. [01501 Synthesis of 3-(4-Amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl) benzenesulfonamide (BA41). A solution of Benzenesulfonamide-3-boronic acid pinacol ester (31 mg, 0.11 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl 1H-pyrazolo[3,4-d]pyrimidin-4-anine (30 mg, 0.10 mmol) in DME (12 mL). Pd(PPh 3

)

4 (30 ) mg, 0.03 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH 2 C1 2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA) to yield BA41 (9.2 mg, 28% yield). ESI-MS (M+H)* m/z calcd 333.1, found 333.0. 5 [0151] Synthesis of 2-(4-amino-1-isopropyl-lH-pyrazolo[3,4-d]pyrimidin-3 yl)benzo[b]thiophene-5-carbaldehyde (BA42). A solution of 5-Formylbenzo[b]thiophene-2 boronic acid pinacol ester (31 mg, 0.11 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (30 mg, 0.10 mmol) in DME (12 mL). Pd(PPh 3

)

4 (30 mg, 0.03 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the 0 reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH 2 Cl 2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA) to yield BA42 (15.2 mg, 45% yield). ESI-MS (M+H)* m/z calcd 338.1, found 338.0. [0152] Synthesis of 5-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-1H-indole 25 3-carbaldehyde (BA43). A solution of N-Boc-3-formyl-5-indoleboronic acid pinacol ester (40 mg, 0.11 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine (30 mg, 0.10 mmol) in DME (12 mL). Pd(PPh 3

)

4 (30 mg, 0.03 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with 30 saturated NaCl and CH 2 Cl 2 . Organic phases were combined, concentrated in vacuo and purified byRP-HPLC (MeCN:H 2 0:0.1% TFA). The TFA from purification hydrolyzed the Boc to yield BA43. ESI-MS (M+H)* m/z called 321.1, found 321.0. 36 WO 2007/114926 PCT/US2007/008395 [0153] Synthesis of 3-(benzo[c][1,2,5]oxadiazol-6-yl)-1-isopropyl-1H-pyrazolo[3,4 d]pyrimidin-4-amine (BA44). A solution of Benzo[c][1,2,5]oxadiazole-5-boronic acid (18 mg, 0.11 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine (30 mg, 0.10 mmol) in DME (12 mL). Pd(PPh 3

)

4 (30 mg, 5 0.03 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCL and CH 2 Cl 2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0. 1% TFA) to yield BA44. ESI-MS (M+H)* m/z calcd 296.1, found 296.1. 0 [0154] Synthesis of 2-(4-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3 yl)phenyl)acetonitrile (BA45). A solution of (4-Cyanomethylphenyl)boronic acid (18 mg, 0.11 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-aniine (30 mg, 0.10 mmol) in DME (12 mL). Pd(PPh 3

)

4 (30 mg, 0.03 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C 5 under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaC1 and CH 2 Cl 2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA) to yield BA45. ESI-MS (M+H)* m/z calcd 293.1, found 293.1. [0155] Synthesis of 2-(3-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3 0 yl)phenyl)acetonitrile (BA46). A solution of (3-Cyanomethylphenyl)boronic acid (18 mg, 0.11 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-iH pyrazolo[3,4-d]pyrimidin-4-amine (30 mg, 0.10 mmol) in DME (12 mL). Pd(PPh 3

)

4 (30 mg, 0.03 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with 25 saturated NaC1 and CH 2 Cl 2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0. 1% TFA) to yield BA45. ESI-MS (M+H)* m/z calcd 293.1, found 293.1. [0156] Synthesis of 1-isopropyl-3-(4-methoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4 amine (BA48). A solution of (4-Methoxyphenylboronic acid (17 mg, 0.11 mmol) in EtOH 30 (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4 amine (30 mg, 0.10 mmol) in DME (12 mL). Pd(PPh) 4 (30 mg, 0.03 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere 37 WO 2007/114926 PCT/US2007/008395 overnight. After cooling, the reaction was extracted with saturated NaCl and CH 2 C12. Organic phases were combined, concentrated in vacuo and purified by RP-HLPLC (MeCN:H 2 0:0.1% TFA) to yield BA48 (4.5mg, 16% yield). ESI-MS (M+H)* m/z calcd 284.1, found 284.1. 5 [0157] Synthesis of 1-isopropyl-3-(3-methoxyphenyl)-1H-pyrazolo[3,4-d]pyriniidin-4 amine (BA49). A solution of 3-Methoxyphenylboronic acid (17 mg, 0.11 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4 amine (30 mg, 0.10 mmol) in DME (12 mL). Pd(PPh 3

)

4 (30 mg, 0.03 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere 0 overnight. After cooling, the reaction was extracted with saturated NaCl and CH 2

C

2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA) to yield BA49. ESI-MS (M+H)* m/z called 284.1, found 284.0. [01581 Synthesis of 1-isopropyl-3-(pyridin-3-yl)-1H-pyrazolo[3,4-djpyrimidin-4-amine (BA52). A solution of 3-Pyridinylboronic acid (15 mg, 0.14 mmol) in EtOH (3.3 mL) was 5 added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (40 mg, 0.13 mmol) in DME (12 mL). Pd(PPh 3

)

4 (15 mg, 0.015 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH 2 Cl 2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0) to yield BA52. 0 ESI-MS (M+H)* m/z calcd 255.1, found 255.0. [0159] Synthesis of 1-isopropyl-3-(pyrimidin-5-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (BA53). A solution of 5-Pyrimidinylboronic acid (15 mg, 0.14 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (40 mg, 0.13 mmol) in DME (12 mL). Pd(PPh 3

)

4 (15 mg, 0.015 mmol) and saturated Na 2

CO

3 (1.9 25 mL) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH 2 Cl 2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0) to yield BA53. ESI-MS (M+H)* m/z calcd 256.1, found 256.1. [0160] Synthesis of 3-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-1-isopropyl-1H-pyrazolo[3,4 30 dlpyrimidin-4-amine (BA54). A solution of 2,3-dihydro-1,4-benzodioxin-6-ylboronic acid (26 mg, 0.14 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine (40 mg, 0.13 mmol) in DME (12 mL). Pd(PPh 3

)

4 (30 mg, 38 WO 2007/114926 PCT/US2007/008395 0.03 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH 2 Cl 2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA) to yield BA54 (6 mg, 15% yield). ESI-MS 5 (M+H)* m/z calcd 312.1, found 312.0. [0161] Synthesis of 1-(3-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3 yl)phenyl)ethanone (BA55). A solution of 3-Acetylphenylboronic acid (23 mg, 0.14 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-IH-pyrazolo[3,4 d]pyrimidin-4-amine (40 mg, 0.13 mmol) in DME (12 mL). Pd(PPh 3

)

4 (30 mg, 0.03 mmol) 0 and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH 2 Cl 2 . Organic phases were combined, concentrated in vacuo and purified by RP HPLC (MeCN:H 2 0:0.1% TFA) to yield BA55 (7 mg, 18% yield). ESI-MS (M+H)* m/z calcd 296.1, found 296.1. 5 [0162] Synthesis of 4-(4-amino-1-isopropyl-IH-pyrazolo[3,4-d]pyrimidin-3-yl)phenol (BA56). A solution of 4-Hydroxyphenylboronic acid (30 mg, 0.14 mmol) in EtOH (3.3 mL) was added to a solution of 3-iodo-1-isopropyl-lH-pyrazolo[3,4-d]pyrimidin-4-amine (40 mg, 0.13 mmol) in DME (12 mL). Pd(PPh 3

)

4 (30 mg, 0.03 mmol) and saturated Na 2

CO

3 (1.9 mL) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After 0 cooling, the reaction was extracted with saturated NaC1 and CH 2 Cl 2 . Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA) to yield BA56 (12 mg, 32% yield). ESI-MS (M+H)* m/z calcd 270.1, found 270.1. [0163] Synthesis of P13-K/Tyrosine Kinase Dual Inhibitors [0164] Synthesis of 1H-pyrazolo[3,4-d]pyrimidin-4-amine (BA18). A solution of 250 ml 25 of formamide and 3-amino-4-pyrazolecarbonitrile (25 g, 6.231 mol) was heated to 180*C overnight under an argon atmosphere. Reaction was cooled and 400 ml of dH20 were added. The resulting solid was filtered and rinsed with cold dH20. White solid precipitate was collected and dried in vacuo overnight to yield BA18 (39g, 100% yield). ESI-MS (M+H)+ m/z calcd 136.1, found 136.1. 30 [0165] Synthesis of 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-anine (BA19). A solution of 3H-pyrazolo[3,4-d]pyrimidin-4-amine (1Og, 0.074 mol) and n-iodo-succinamide (25 g, 0.111 39 WO 2007/114926 PCT/US2007/008395 mol) in DMF (80ml) was heated to 80*C overnight under an argon atmosphere. The resulting solid was filtered and rinsed with cold EtOH. Product was dried in vacuo overnight to yield BA19 (24g, 100% yield). ESI-MS (M+H)+ m/z calcd 262.0, found 262.0 [01661 Synthesis of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (BA12). A 5 solution of 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine (2 g, 0.0077 mol) and K2C03 (4.2g, 0.031 mol) in DMF (50 ml) was brought to 80*C under an argon atomosphere. Isopropylbromide (1.0g, 0.0084 mol) was added with a syringe. Reaction was refluxed under argon atmosphere for 2 hours. Solid K2C03 was removed by filtration. Solvent was partially removed in vacuo. Sodium citrate (50 ml) was added and reaction was extracted D with EtOAc. Organic phases concentrated in vacuo and purified using silica gel column chromatography [MeOH--CH2CI2, 5:95] yielding BA12 (1.68 g, 72% yield). ESI-MS (M+H)+ m/z calcd 304.0, found 304.1. [01671 Synthesis of 4-(4-Amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl) benzenesulfonamide (BA14). A solution of benzenesulfonamide-4-boronic acid pinacol ester 5 (23 mg, 0.08 nmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine (20 mg, 0.07 mmol) in DME (12 ml). Pd(PPh3)4 (16 mg, 0.014 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80'C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCI and CH2Cl2. Organic phases were combined, concentrated in vacuo and 0 purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA14 (2.2 mg, 10% yield). ESI-MS (M+H)+ m/z calcd 333.1, found 333.1. [0168] Synthesis of 1-isopropyl-3-(3-methoxy-4-methylphenyl)-1H-pyrazolo[3,4 d]pyrimidin-4-amine (BA15). A solution of 2 methoxy-4-(4,4,5,5-tetramethyl-1,3-2 dioxaborolan-2-yl) phenol (19 mg, 0.08 mmol) in EtOH (3.3 ml) was added to a solution of 25 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (20 mg, 0.07 mmol) in DME (12 ml). Pd(PPh3)4 (16 mg, 0.014 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA15 (4.3 30 mg, 20% yield). ESI-MS (M+H)+ m/z calcd 300.1, found 300.2. [0169] Synthesis of 6-(4-amino-1-isopropyl-lH-pyrazolo[3,4-d]pyrimidin-3-yl)naphthalen 2-ol (BA17). A solution of 6-hydroxynaphthalen-2-yl-2-boronic acid (15 mg, 0.08 mmol) in 40 WO 2007/114926 PCT/US2007/008395 EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-lH-pyrazolo[3,4-d]pyrimidin 4-amine (20 mg, 0.07 mmol) in DME (12 ml). Pd(PPh3)4 (16 mg, 0.014 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCI and 5 CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA15 (4.8 mg, 23% yield). ESI-MS (M+H)+ m/z calcd 320.1, found 320.1. [0170] Synthesis of tert-butyl 4-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl) 2-methoxyphepylcarbamate (BA20). A solution of 4 4-N-Boc-amino-3-methoxy D benzeneboronic acid (48 mg, 0.18 mmol) in EtOH (3.3 ml) was added to a solution of 3 iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (50 mg, 0.18 mmol) in DME (12 ml). Pd(PPh3)4 (40 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCL and CH2C12. Organic phases were combined, 5 concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA20. ESI-MS (M+H)+ m/z calcd 399.2, found 399.1. [0171] Synthesis of 3-(4-amino-3-methoxyphenyl)-1-isopropyl-1H-pyrazolo[3,4 d]pyrimidin-4-amine (BA20d). A solution of tert-butyl 4-(4-amino-1-isopropyl-lH pyrazolo[3,4-d]pyrimidin-3-yl)-2-methoxyphenylcarbamate (BA20) (20 mg, 0.05 mmol) in 0 CH2C12, TFA, S(CH2)2, H20 (45:45:5:5) (1ml) was stirred at room temperature for 15 minutes. NaHCO3 (2 ml) was added till reaction was alkaline. Reaction was extrated with H20 and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA20d. [0172] Synthesis of 2-amino-5-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3 25 yl)phenol (BA20dd). BA20 (tert-butyl 4-(4-amino-1-isopropyl-lH-pyrazolo[3,4 d]pyrimidin-3-yl)-2-methoxyphenylcarbanate, 7 mg, 0.018 mmol) was dissolved in CH2Cl2 (2.5 ml) and stirred under an argon atmosphere at room temperature. BBr3 (0.500 ml) was added slowly with a syringe. The reaction mixture was stirred overnight, under argon at room temperature. BBr3 was removed in vacuo and the remaining solid was purified by RP 30 HIPLC (MeCN:H20:0.1% TFA) to yield BA20dd. [0173] Synthesis of 5-(4-anino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)pyridine-2 carbonitrile (BA21). A solution of 2-cyanopyridine 5-boronic acid pinocol ester (18 mg, 41 WO 2007/114926 PCT/US2007/008395 0.08 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine (20 mg, 0.07 mmol) in DME (12 ml). Pd(PPh3)4 (16 mg, 0.014 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with 5 saturated NaCl and CH2C12. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA21 (2.5 mg, 14% yield). ESI-MS (M+H)+ m/z calcd 280.1, found 280.1. [0174] Synthesis of 3-(3-(benzyloxy)-5-fluorophenyl)-1-isopropyl-1H-pyrazolo[3,4 d]pyrimidin-4-amine. A solution of (3-Benzyloxy-5-fluorophenyl)boronic acid (29 mg, 5.80 D mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H-lyrazolo[3;4 d]pyrimidin-4-amine (20 mg, 0.07 mmol) in DME (12 ml). Pd(PPh3)4 (16 mg, 0.014 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP 5 HPLC (MeCN:H20:0.1% TFA) to yield BA22 (15.6 mg, 60% yield). ESI-MS (M+H)+ m/z calcd 378.1, found 378.0. [0175] Synthesis of 3-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-5 fluorophenol (BA22). A solution of -(3-(benzyloxy)-5-fluorophenyl)-1-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine (15 mg, 0.04 mmol) in MeOH (0.9 ml) was flushed with 0 argon. Pd on activated carbon (10 ml) was carefully added while keeping reaction under an argon atmosphere. Reaction was flushed with H2 gas and left under H2 atmosphere overnight at room temperature. The reaction was filtered through celite and rinsed with MeOH to yield BA22 (15 mg, 100% yield). ESI-MS (M+H)+ m/z calcd 288.1, found 288.1. [01761 Synthesis of 1-isopropyl-3-(3,4-dimethoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4 25 amine (BA23). A solution of 3,4-Dimethoxyphenylboronic acid (24 mg, 0.13 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin 4-amine (20 mg, 0.07 mmol) in DME (12 ml). Pd(PPh3)4 (16 mg, 0.014 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and 30 CH2C12. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA23 (13.1 mg, 60% yield). ESI-MS (M+H)+ m/z calcd 314.0, found 314.1. 42 WO 2007/114926 PCT/US2007/008395 [0177] Synthesis of tert-butyl 2-(4-amino-1-isopropyl-f1-pyrazolo[3,4-d]pyrimidin-3-yl) 5-(benzyloxy)-1H-indole-1-carboxylate (BA24). A solution of 5-Benzyloxy-1-BOC-indole 2-boronic acid (303mg, 0.83 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1 isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (100 mg, 0.33 mmol) in DME (12 ml). 5 Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2C03 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCL and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by silica gel column chromatography [EtOAc-hexanes, 5:95] to yield BA24. ESI-MS (M+H)+ m/z calcd 499.2, found 499.2. 0 [0178] Synthesis of 2-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-1H-indol 5-ol (BA24dd). BA24 (3-(4-fluoro-3-methoxyphenyl)-l-isopropyl-IH-pyrazolo[3,4 d]pyrimidin-4-amine, 30 mg, 0.10 mmol) was dissolved in a solution of formic acid (4.5 ml, 10 equivalents) and HCl (0.45 ml, 1 equivalent). The reaction was heated and stirred for one hour under an argon atmosphere. The reaction was then concentrated in vacuo and purified 5 by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA24dd. ESI-MS (M+H)+ m/z called 309.1, found 309.1. [0179] Synthesis of (3-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3 yl)phenyl)methanol (BA26). A solution of (3-Hydroxymethylphenyl)boronic acid (24 mg, 0.13 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H o pyrazolo[3,4-d]pyrimidin-4-amine (20 mg, 0.07 mmol) in DME (12 ml). Pd(PPh3)4 (16mg, 0.014 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80"C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2C12. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA26 (8.4 mg, 42% yield). ESI-MS 25 (M+H)+ m/z calcd 283.1, found 284.2. [01801 Synthesis of 3-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-N-(4,5 dihydrothiazol-2-yl)benzamide (BA30). A solution of [3-((4,5-dihydrothiazol-2 yl)carbamoyl)phenyl]boronic acid (19 mg, 0.08 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (20 mg, 0.07 mmol) in 30 DME (12 ml). Pd(PPh3)4 (16 mg, 0.014 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaC1 and CH2C12. Organic phases were combined, 43 WO 2007/114926 PCT/US2007/008395 concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA30 (17.8 mg, 67% yield). [01811 Synthesis of 1-(4-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3 yl)phenyl)ethanone (BA31). A solution of 4-Acetylphenylboronic acid (12.7 mg, 0.08 mmol) 5 in EtOH (3.3 ml) was added to a solution of 3-iodo-l-isopropyl-lH-pyrazolo[3,4 d]pyrimidin-4-amine (20 mg, 0.07 mmol) in DME (12 ml). Pd(PPh3)4 (16 mg, 0.014 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCI and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP ) HPLC (MeCN:H20:0.1% TFA) to yield BA31 (12.9 mg, 62% yield). [01821 Synthesis of (3-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3 yl)phenyl)methanol (BA32). A solution of (4-Aminocarbonyl-3-chlorophenyl)boronic acid (16 mg, 0.08 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine (20 mg, 0.07 mmol) in DME (12 ml). Pd(PPh3)4 (16 mg, 5 0.014 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80'C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA32 (9.7 mg, 42% yield). ESI-MS (M+H)+ m/z calcd 331.1, found 331.1. 0 [0183] Synthesis of 5-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-3 methylthiophene-2-carbaldehyde (BA34). A solution of 5-Formyl-3-methylthiophene-2 boronic acid (26 mg, 0.14 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1 isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (40 mg, 0.13 mmol) in DME (12 ml). Pd(PPh3)4 (16 mg, 0.014 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction 25 was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0. 1% TFA) to yield BA34 (14.7 mg, 38% yield). ESI-MS (M+H)+ m/z calcd 302.1, found 302.0. [0184] Synthesis of 5-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)furan-3 30 carbaldehyde (BA35). A solution of 4-Formylfuran-2-boronic acid (20 mg, 0.14 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin 4-amine (40 mg, 0.13 mmol) in DME (12 ml). Pd(PPh3)4 (16 mg, 0.014 mmol) and 44 WO 2007/114926 PCT/US2007/008395 saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCL and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA35 (13.5 mg, 39% yield). ESI-MS (M+H)+ m/z called 5 272.1, found 272.1. [01851 Synthesis of N-[3-(4-Amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl) phenyl]-methanesulfonamide (BA38). A solution of 3-Methanesulfonylaminophenylboronic acid (32 mg, 0.15 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl 1H-pyrazolo[3,4-d]pyrimidin-4-amine (40 mg, 0.13 mmol) in DME (12 ml). Pd(PPh3)4 (16 3 mg, 0.014 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80"C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCI and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HIPLC (MeCN:H20:0.1% TFA) to yield BA38 (24.3 mg, 54% yield). ESI-MS (M+H)+ m/z calcd 347.1, found 347.0. 5 [0186] Synthesis of 3-(4-anino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)benzonitrile (BA39). A solution of 3-Cyanophenylboronic acid (23 mg, 0.15 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (40 mg, 0.13 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80'C under an argon atmosphere overnight. After 0 cooling, the reaction was extracted with saturated NaCI and CH2C12. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0. 1% TFA) to yield BA39 (14.9 mg, 41% yield). ESI-MS (M+H)+ m/z calcd 279.1, found 279.0. [0187] Synthesis of N-[4-(4-Amino-l-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl) phenyl]-methanesulfonamide (BA40). A solution of 4-Methanesulfonylaminophenylboronic 25 acid (24 mg, 0.11 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl 1H-pyrazolo[3,4-d]pyrimidin-4-anine (30 mg, 0.10 nnol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2Cl2. Organic phases were combined, concentrated in vacuo and 30 purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA40 (0.9 mg, 3% yield). ESI-MS (M+H)+ m/z called 347.1, found 347.0. 45 WO 2007/114926 PCT/US2007/008395 [0188] Synthesis of 3-(4-Amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl) benzenesulfonamide (BA41). A solution of Benzenesulfonarnide-3-boronic acid pinacol ester (31 mg, 0.11 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-l -isopropyl 1H-pyrazolo[3,4-d]pyrimidin-4-amine (30 mg, 0.10 mmol) in DME (12 ml). Pd(PPh3)4 (30 5 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA41 (9.2 mg, 28% yield). ESI-MS (M+H)+ m/z calcd 333.1, found 333.0. D [01891 Synthesis of 2-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3 yl)benzo[b]thiophene-5-.carbaldehyde (BA42). A solution of 5-Formylbenzo[b]thiophene-2 boronic acid pinacol ester (31 mg, 0.11 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-l-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (30 mg, 0.10 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the 5 reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA42 (15.2 mg, 45% yield). ESI-MS (M+H)+ m/z calcd 338.1, found 338.0. [01901 Synthesis of 5-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-lH-indole 0 3-carbaldehyde (BA43). A solution of N-Boc-3-formyl-5-indoleboronic acid pinacol ester (40 mg, 0.11 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine (30 mg, 0.10 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with 25 saturated NaCl and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA). The TFA from purification hydrolyzed the Boc to yield BA43. ESI-MS (M+H)+ m/z 6alcd 321.1, found 321.0. [0191] Synthesis of 3-(benzo[c][1,2,5]oxadiazol-6-yl)-1-isopropyl-1H-pyrazolo[3,4 d]pyrimidin-4-amine (BA44). A solution of Benzo[c][1,2,5]oxadiazole-5-boronic acid (18 30 mg, 0.11 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine (30 mg, 0.10 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C 46 WO 2007/114926 PCT/US2007/008395 under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaC1 and CH2C12. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA44. ESI-MS (M+H)+ m/z calcd 296.1, found 296.1. [01921 Synthesis of 2-(4-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3 yl)phenyl)acetonitrile (BA45). A solution of (4-Cyanomethylphenyl)boronic acid (18 mg, 0.11 mmnol) in EtOH (3.3 ml) was added to a solution of 3-iodo-l-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine (30 mg, 0.10 nmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C ) under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaC1 and CH2C12. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA45. ESI-MS (M+H)+ m/z calcd 293.1, found 293.1. [0193] Synthesis of 2-(3-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3 5 yl)phenyl)acetonitrile (BA46). A solution of (3-Cyanomethylphenyl)boronic acid (18 mg, 0.11 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine (30 mg, 0.10 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with ) saturated NaCl and CH2C12. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA45. ESI-MS (M+H)+ m/z called 293.1, found 293.1. [0194] Synthesis of 1-isopropyl-3-(4-methoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4 amine (BA48). A solution of (4-Methoxyphenylboronic acid (17 mg, 0.11 mmol) in EtOH !5 (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4 amine (30 mg, 0.10 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCI and CH2C12. Organic phases were combined, concentrated in vacuo and purified by RP-H{PLC 0 (MeCN:H20:0.1% TFA) to yield BA48 (4.5mg, 16% yield). ESI-MS (M+H)+ m/z called 284.1, found 284.1. 47 WO 2007/114926 PCT/US2007/008395 [01951 Synthesis of 1-isopropyl-3-(3-methoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4 amine (BA49). A solution of 3-Methoxyphenylboronic acid (17 mg, 0.11 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4 amine (30 mg, 0.10 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA49. ESI-MS (M+H)+ m/z calcd 284.1, found 284.0. [01961 Synthesis of 1-isopropyl-3-(pyridin-3-yl)-IH-pyrazolo[3,4-d]pyrimidin-4-amine ) (BA52). A solution of 3-Pyridinylboronic acid (15 mg, 0.14 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (40 mg, 0.13 mmol) in DME (12 ml). Pd(PPh3)4 (15 mg, 0.015 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2C12. Organic phases were 5 combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20) to yield BA52. ESI-MS (M+H)+ m/z calcd 255.1, found 255.0. [01971 Synthesis of 1-isopropyl-3-(pyrimidin-5-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (BA53). A solution of 5-Pyrimidinylboronic acid (15 mg, 0.14 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (40 mg, 0.13 0 mmol) in DME (12 ml). Pd(PPh3)4 (15 mg, 0.015 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20) to yield BA53. ESI-MS (M+H)+ m/z calcd 256.1, found 256.1. 25 [0198] Synthesis of 3-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-1-isopropyl-1H-pyrazolo[3,4 d]pyrimidin-4-amine (BA54). A solution of 2,3-dihydro-1,4-benzodioxin-6-ylboronic acid (26 mg, 0.14 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-l-isopropyl-1H pyrazolo[3,4-dlpyrimidin-4-amine (40 mg, 0.13 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C 30 under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2Cl2. Organic phases were combined, concentrated in vacuo and 48 WO 2007/114926 PCT/US2007/008395 purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA54 (6 mg, 15% yield). ESI-MS (M+H)+ m/z calcd 312.1, found 312.0. [01991 Synthesis of 1-(3-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3 yl)phenyl)ethanone (BA55). A solution of 3-Acetylphenylboronic acid (23 mg, 0.14 mmol) 5 in EtOH (3.3 ml) was added to a solution of 3-iodo-l-isopropyl-1H-pyrazolo[3,4 d]pyrimidin-4-amine (40 mg, 0.13 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80'C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaC1 and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP D HPLC (MeCN:H20:0.1% TFA) to yield BA55 (7 mg, 18% yield). ESI-MS (M+H)+ m/z calcd 296.1, found 296.1. [02001 Synthesis of 4-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)phenol (BA56). A solution of 4-Hydroxyphenylboronic acid (30 mg, 0.14 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (40 mg, 5 0.13 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA56 (12 mg, 32% yield). ESI-MS (M+H)+ m/z calcd 270.1, found 270.1. 0 [0201] Synthesis of 4-(4-amino-1-isopropyl-lH-pyrazolo[3,4-d]pyrimidin-3-yl)-2 fluorophenol (BA59). A solution of 3-fluoro-4-hydroxyphenylboronic acid (103 mg, 0.66 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4 d]pyrimidin-4-amine (100 mg, 0.33 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an 25 argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaC1 and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP using silica gel column chromatography [MeOH-CH2Cl2, 2:98] to yield BA59 (26 mg, 27% yield). ESI-MS (M+H)+ m/z calcd 288, found 288. [0202] Synthesis of 4-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-3 30 methylphenol (BA60). A solution of 4-hydroxy-2-methylphenylboronic acid (110 mg, 0.66 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4 d]pyrimidin-4-amine (100 mg, 0.33 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) 49 WO 2007/114926 PCT/US2007/008395 and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaC1 and CH2C12. Organic phases were combined, concentrated in vacuo and purified by silica gel column chromatography [MeOH-CH2Cl2, 2:98] to yield BA60 (42 mg, 22% yield). ESI-MS (M+H)+ m/z calcd 284, found 284. [02031 Synthesis of 3-(4-fluoro-3-methoxyphenyl)-1-isopropyl-1H-pyrazolo[3,4 d]pyrimidin-4-amine (BA62). A solution of 4-fluoro-3-methoxyphenylboronic acid (61 mg, 0.36 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-l-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine (9.0 mg, 0.30 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, ) 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2C12. Organic phases were combined, concentrated in vacuo and purified by silica gel column chromatography [MeOH-CH2C12, 2:98] to yield BA62 (40 mg, 44% yield). ESI-MS (M+H)+ m/z called 302, found 302. 5 [0204] Synthesis of 5-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)- 2 fluorophenol (BA62d). A solution of BA62 (3-(4-fluoro-3-methoxyphenyl)-1-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine, 30 mg, 0.10 mmol) was dissolved in CH2C12 (5 ml) and stirred under an argon atmosphere. BBr3 (500uL, 0.5 mol) was added slowly with a syringe, while stirring. The reaction was stirred at room temperature for 3 hours then D concentrated in vacuo and purified using silica gel column chromatography [MeOH CH2CI2, 2:98] to yield BA62d (23 mg, 44% yield). ESI-MS (M+H)+ m/z called 288.1, found 288.1. [0205] Synthesis of 3-(2,5-difluoro-4-methoxyphenyl)-1-isopropyl-1H-pyrazolo[3,4 d]pyrimidin-4-amine (BA63). A solution of 2,5-difluoro-4-methoxyphenylboronic acid (84 25 mg, 0.45 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine (54 mg, 0.18 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2C12. Organic phases were combined, concentrated in vacuo and 30 purified by silica gel column chromatography [MeOH-CH2Cl2, 2:98] to yield BA63 (50 mg, 17% yield). ESI-MS (M+H)+ m/z calcd 320.1, found 320.0. 50 WO 2007/114926 PCT/US2007/008395 [0206] Synthesis of 4-(4-amino-1-isopropyl-IH-pyrazolo[3,4-d]pyrimidin-3-yl)-2,5 difluorophenol (BA93). 3-(2,5-difluoro-4-methoxyphenyl)-1-isopropyl-1H-pyrazolo[ 3

,

4 d]pyrimidin-4-amine (BA63) (20 mg, 0.06 nmol) was dissolved in CH2Cl2 (2ml) and BBr3 (0.630 mL, 0.63 mmol) was added slowly with a syringe, while stirring. The reaction was i stirred at room temperature for overnight then concentrated in vacuo and purified using by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA93 (6.7 mg, 35% yield). ESI-MS (M+H)+ m/z calcd 306.1, found 306.0. [0207] Synthesis of 1-isopropyl-3-(3,4,5-trimethoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin 4-amine (BA64). A solution of 3,4,5-trimethoxyphenylboronic acid (123 mg, 0.58 mmol) in ) EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimnidin 4-amine (70 mg, 0.23 mm 6 l) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2C12. Organic phases were combined, concentrated in vacuo and purified by silica gel column 5 chromatography [MeOH-CH2Cl2, 2:98] to yield BA64 (70 mg, 89% yield). ESI-MS (M+H)+ m/z calcd 344.1, found 344.0. [0208] Synthesis of 1-isopropyl-3-(2,3-dimethoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4 amine (BA65). A solution 2,3-dimethoxyphenylboronic acid (105 mg, 0.58 mmol) in EtOH (3.3 ml) was added sto a solution of 3-iodo-1-isopropyl-1IH-pyrazolo[3,4-d]pyrimidin-4 0 amine (70 mg, 0.23 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2C12. Organic phases were combined, concentrated in vacuo and purified by silica gel column chromatography [MeOH-CH2Cl2, 2:98] to yield BA65 (63 mg, 88% yield). ESI-MS 25 (M+H)+ m/z calcd 314.1, found 314.1. [0209] Synthesis of 1-isopropyl-3-(2,4-dimethoxypyrimidin-5-yl)-1H-pyrazolo[3,4 d]pyrimidin-4-amine (BA66). A solution 2,4-dimethoxypyrimidin-5-yl-5-boronic acid (106 mg, 0.58 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine (70 mg, 0.23 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 30 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2CI2. Organic phases were combined, concentrated in vacuo and 51 WO 2007/114926 PCT/US2007/008395 purified by silica gel column chromatography [MeOH-CH2Cl2, 2:98] to yield BA66. ESI MS (M+H)+ m/z called 316.1, found 316.0. [02101 Synthesis of 1-cyclopentyl-3-(3-fluoro-5-methoxyphenyl)-1H-pyrazolo[3,4 d]pyrimidin-4-amine (BA79). 3-fluoro-5-methoxybenzoic acid (5 g, 0.029 mol) was stirred 5 in CH2Cl2 (50ml) at 0*C under an argon atmosphere. DMF (9 drops, catalytic) was added, followed by oxalyl chloride (12.7 ml, 0.147 mol). Reaction was warmed to room temperature then stirred under argon for one hour. Reaction was concentrated in vacuo to yield 3-fluoro 5-methoxybenzoyl chloride (BA67). [0211] A solution of malononitrile (2.87 g, 0.044 mol) in dry THF (50 ml) was stirred at 3 0*C under an argon atmosphere. Nal in paraffin oil (4.64 g, 0.116 mol) was added piece wise to solution. 3-fluoro-5-methoxybenzoyl chloride (BA67, 0.029 mol) was dissolved in 50 ml dry THF and added slowly to reaction. Reaction was warmed to room temperature and stirred under argon for 24 hours. 1N HCI (200 ml) was slowly added, then reaction mixture was extracted with EtOAc. Organic phases were combined, dried with magnesium sulfate, 5 then concentrated in vacuo to yield 2-((3-fluoro-5 methoxyphenyl)(methoxy)methylene)malononitrile (BA69). [0212] 2-((3-fluoro-5-methoxyphenyl)(methoxy)methylene)malononitrile (BA69, 0.029 mol) stirred in EtOH (20ml) at room temperature under an argon atmosphere. Hydrazine (1.4 ml, 29 mmol) was added and reaction was left stirring for 90 minutes. Reaction mixture was 0 concentrated in vacuo and dried on vacuum pump overnight to yield intermediate 5-amino-3 (3-fluoro-5-methoxyphenyl)-1H-pyrazole-4-carbonitrile (BA73). Formamide (20ml) was added and reaction was heated to 180 0 C under an argon atmosphere overnight. Reaction was cooled and dH2O was added (40ml) forcing a white precipitate out of solution. Precipitate was collected and washed with dH20. Solid was dried and purified by silica gel column 25 chromatography [MeOH-CH2Cl2, 10:90] to yield 3-(3-fluoro-5-methoxyphenyl)-1H pyrazolo[3,4-d]pyrimidin-4-amine (BA75). [02131 3-(3-fluoro-5-methoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (BA75, 100 mg, 0.386 mmol) was dissolved in DMF (10 ml). K2C03 (250 mg, 1.54 mmol) was added and reaction was stirred at room temperature under an argon atmosphere. Iodocyclopentane 30 (0.134 ml, 1.16 mmol) was added with a syringe and reaction was stirred for 2 hours. Solid K2C03 was removed by filtration. Solvent was partially removed in vacuo. Sodium citrate 52 WO 2007/114926 PCT/US2007/008395 (50 ml) was added and reaction was extracted with EtOAc. Organic phases concentrated in vacuo and purified using by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA79. [0214] Synthesis of 1-cyclopentyl-3-(3-fluoro-5-methoxyphenyl)-1H-pyrazolo[3,4 d]pyrimidin-4-amine (BA79d). 1-cyclopentyl-3-(3-fluoro-5-methoxyphenyl)-1H 5 pyrazolo[3,4-d]pyrimidin-4-amine (BA79, 0.386 mmol) was dissolved in CH2C12 (2 ml). BBr3 (4 mL, 4 mol) was added slowly with a syringe, while stirring. The reaction was stirred at room temperature for 2 hours then concentrated in vacuo and purified using by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA79 (69 mg, 57% yield). [02151 Synthesis of 1-cyclopentyl-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine (BA80). D A solution of 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine (400 mg, 1.53 mmol) and K2C03 (1 g, 6 mmol) in DMF (5 ml) was stirred at room temperature under an argon atomosphere. lodocyclopentane (1.0g, 0.0084 mol) was added with a syringe. Reaction was refluxed under argon atmosphere for 2 hours. Solid K2C03 was removed by filtration. Solvent was partially removed in vacuo. Sodium citrate (50 ml) was added and reaction was 5 extracted with EtOAc. Organic phases concentrated in vacuo and purified using silica gel column chromatography [MeOH--CH2C12, 5:95] yielding BA80 (300 mg, 60% yield). ESI MS (M+H)+ m/z calcd 330.0, found 330.0. [0216] Synthesis of 1-(3-(4-amino-1-isopropyl-lH-pyrazolo[3,4-d]pyrimidin-3 yl)phenyl)ethanone (BA81, BA81d & BA81dd). A solution of tert-butyl 2-methoxy-4 0 (4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylcarbamate (200 mg, 0.76 mmol) in EtOH (3.3 ml) was added to a solution of 1-cyclopentyl-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4 amine (BA80, 100 mg, 0.30 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80"C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and 25 CH2Cl2. Organic phases were combined, concentrated in vacuo and purified using silica gel column chromatography [MeOH--CH2Cl2, 5:95] yielding BA81. BA81 was dissolved in 50:50 CH2Cl2:TFA and stirred for one hour at room temperature. The reaction mixture was concentrated in vacuo and purified using by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA81d. BA81d was dissolved in CH2C12 (2ml) and BBr3 (4 mL, 4 mol) was added slowly 30 with a syringe, while stirring. The reaction was stirred at room temperature for 2 hours then concentrated in vacuo and purified using by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA81dd. 53 WO 2007/114926 PCT/US2007/008395 [02171 Synthesis of 3-(3-bromo-5-methoxyphenyl)-1-isopropyl-1H-pyrazolo[3,4 d]pyrimidin-4-amine (BA85). A solution of 2-(3-bromo-5-methoxyphenyl)-4,4,5,5 tetramethyl-1,3,2-dioxaborolane (137 mg, 0.43 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-IH-pyrazolo[3,4-d]pyrimidin-4-amnine (65 mg, 0.216 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2C03 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaC1 and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA85 (28mg, 36% yield). ESI-MS (M+H)+ m/z calcd 362.1, found 362.0. [02181 Synthesis of 3-(4-amino-1-isopropyl-lH-pyrazolo[3,4-d]pyrimidin-3-yl)-5 bromophenol (BA87). 3-(3-bromo-5-methoxyphenyl)-1-isopropyl-1H-pyrazolo[3,4 d]pyrimidin-4-amine (BA85, 0.1 mmol) was dissolved in CH2Cl2 (1 ml) and BBr3 (1 mL, 1 mol) was added slowly with a syringe, while stirring. The reaction was stirred at room temperature for 35 minutes then concentrated in vacuo and purified using by RP-HPLC 5 (MeCN:H20:0.1% TFA) to yield BA87 (10.7 mg, 31% yield). ESI-MS (M+H)+ m/z calcd 348.0, found 348.0. [0219] Synthesis of tert-butyl 5-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl) 1H-indole-1-carboxylate (BA86). A solution of tert-butyl 5-(4,4,5,5-tetramethyl-1,3,2 dioxaborolan-2-yl)-1H-indole-1-carboxylate (212 mg, 0.61 mmol) in EtOH (3.3 ml) was 3 added to a solution of 3-iodo-l-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (75 mg, 0.25 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCI and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20) to yield BA86 (9.3 .5 mg, 9% yield). ESI-MS (M+H)+ m/z calcd 362.1, found 362.0. [0220] Synthesis of 3-(1H-indol-5-yl)-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (BA89). Tert-butyl 5-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-1H-indole-1 carboxylate (BA86, 9 mg, 0.022 mmol) was dissolved in 50:50 CH2Cl2:TFA and stirred for one hour at room temperature. The reaction mixture was concentrated in vacuo and purified 50 using by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA89 (4.8 mg, 75% yield). ESI-MS (M+H)+ m/z calcd 293.1, found 293.0. 54 WO 2007/114926 PCT/US2007/008395 [02211 Synthesis of tert-butyl 5-(4-amino-1-cyclopentyl-1H-pyrazolo[3,4-d]pyrimidin-3 yl)-1H-indole-1-carboxylate (BA88). A solution of tert-butyl 5-(4,4,5,5-tetramethyl-1,3,2 dioxaborolan-2-y)-1H-indole--carboxylate (130 mg, 0.38 mmol) in EtOH (3.3 ml) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (50 mg, 0.15 5 mmol) in DME (12 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (1.9 ml) were added and the reaction was heated to 80"C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2C12. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20) to yield BA88. ESI-MS (M+H)+ m/z calcd 419.2, found 419.1. D [0222] Synthesis of 3-(1H-indol-5-yl)-l-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (BA94). Tert-butyl 5-(4-amino-1-cyclopentyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-1H-indole 1-carboxylate (BA88) was dissolved in 50:50 CH2Cl2:TFA and stirred for one hour at room temperature. The reaction mixture was concentrated in vacuo and purified using by RP HPLC (MeCN:H20:0.1% TFA) to yield BA89 (6.3 mg). ESI-MS (M+H)+ m/z calcd 319.1, 5 found 319.2. [02231 Synthesis of 1-cyclopentyl-3-(3,4-dimethoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin 4-amine (BA90). A solution of 3,4-dimethoxyphenylboronic acid (41 mg, 0.23 mmol) in EtOH (1.65ml) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin 4-amine (30 mg, 0.09 mmol) in DME (6 ml). Pd(PPh3)4 (30 mg, 0.03 nmol) and saturated 0 Na2CO3 (0.95 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCI and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H2O) to yield BA90 (8.4 mg, 28% yield). ESI-MS (M+H)+ m/z called 340.2, found 340.1. 25 [02241 Synthesis of 3-(1H-indol-4-yl)-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (BA91). A solution of 1H-indol-4-yl-4-boronic acid (40 mg, 0.25 mmol) in EtOH (1.65 ml) was added to a solution of 3-iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (30 mg, 0.1 mmol) in DME (6 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (0.95 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After 30 cooling, the reaction was extracted with saturated NaCi and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA91 (14.6 mg, 50% yield). ESI-MS (M+H)+ m/z calcd 293.1, found 293.1. 55 WO 2007/114926 PCT/US2007/008395 [0225] Synthesis of 1-cyclopentyl-3-(1H-indol-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (BA92). A solution of 1H-indol-4-yl-4-boronic acid (30 mg, 0.19 mmol) in EtOH (1.65 ml) was added to a solution of 3-iodo-l-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (25 mg, 0.076 mmol) in DME (6 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (0.95 5 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaC1 and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0. 1% TFA) to yield BA92 (23 mg, 95% yield). ESI-MS (M+H)+ m/z calcd 319.2, found 319.1. [0226] Synthesis of 3-(2,3-dihydrobenzofuran-5-yl)-1-isopropyl-1H-pyrazolo[3,4 3 d]pyrimidin-4-amine (BA95). A solution of 2,3-dihydro-l-benzofuran-5-ylboronic acid (38 mg, 0.23 mmol) in EtOH (1.65 ml) was added to a solution of 3-iodo-1-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine (30 mg, 0.1 mmol) in DME (6 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (0.95 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with 5 saturated NaC1 and CH2C12. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA95 (15.7 mg, 59% yield). ESI MS (M+H)+ n/z caled 296.1, found 296.1. [02271 Synthesis of 3-(benzofuran-5-yl)-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (BA96). A solution of 5-(4,4,5,5-tetranethyl-1,3,2-dioxaborolan-2-yl)-1-benzofuran (56 mg, 0 0.23 mmol) in EtOH (1.65 ml) was added to a solution of 3-iodo-1-isopropyl-1H pyrazolo[3,4-d]pyrimidin-4-amine (30 mg, 0.1 mmol) in DME (6 ml). Pd(PPh3)4 (30 mg, 0.03 mmol) and saturated Na2CO3 (0.95 ml) were added and the reaction was heated to 80*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2C12. Organic phases were combined, concentrated in vacuo and Z5 purified by RP-IPLC (MeCN:I420:0.1% TFA) to yield BA96 (19 mg, 72% yield). ESI-MS (M+H)+ m/z calcd 296.1, found 296.1. [02281 Synthesis of 5-(4-amino-1-cyclopentyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-2 ethoxyphenol (BA98). 1-cyclopentyl-3-(4-ethoxy-3-methoxyphenyl)-1H-pyrazolo[3,4 d]pyrimidin-4-amine (ZK359, 25 mg, 0,071 mmol) was dissolved in CH2Cl2 (5 ml) and 30 stirred at -10 0 C under an argon atmosphere. After 30 minutes, reaction was brought to 0*C and stirred for 2.5 hours. Reaction was stirred for additional 4 hours at room temperature, 56 WO 2007/114926 PCT/US2007/008395 then concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0. 1% TFA) to yield BA98 (3 mg, 13 % yield). ESI-MS (M+H)+ m/z calcd 340.1, found 340.1. [0229] Synthesis of 2-(4-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-2 methoxyphenylamino)propan-1-ol (BA99). 3-(4-amino-3-methoxyphenyl)-1-isopropyl-1H 5 pyrazolo[3,4-d]pyrimidin-4-amine (BA20d) (30 mg, 0.10 mmol) was dissolved in DMF (0.400 ml). K2C03 (55 mg, 0.4 mmol) was added and reaction was stirred at 70*C. 3-bromo 1-propanol (0.050 ml, 0.6 mmol) was added and reaction was stirred overnight. Solid K2C03 was removed by filtration. Solvent was partially removed in vacuo. Sodium citrate (50 ml) was added and reaction was extracted with saturated NaCl and CH2Cl2. Organic 3 phases concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA99 (8.4 mg, 24 % yield). ESI-MS (M+H)+ m/z calcd 357.2, found 357.1. [0230] Synthesis of 3-iodo-1-methyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (BA109). A solution of 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine (2 g, 7.69 mmol) and K2C03 (4.25 g, 30.8 mmol) in DMF (5 ml) was stirred at room temperature under an argon atomosphere. 5 lodomethane (1.17 ml, 7.69 mmol) was added with a syringe. Reaction was stirred under an argon atmosphere at room temperature for 2 hours. Solid K2CO3 was removed by filtration. Solvent was partially removed in vacuo. Sodium citrate (50 ml) was added and reaction was extracted with EtOAc. Organic phases concentrated in vacuo and purified using silica gel column chromatography [MeOH--CH2Cl2, 5:95] yielding BA109 (212 mg, 10% yield). 0 ESI-MS (M+H)+ m/z calcd 275.9, found 275.9 [0231] General synthetic scheme for BA102, BA105-108, BA110, BA118, BA128-BA135, BA137, BA139-140, BA143, BA147, BA149-BA152, BA156, BA158, BA160-BA162. A solution of boronic acid (2.5 equivalents) in EtOH (1.65 ml) was added to a solution of 3 iodo-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (BA12, 1 equivalent) in DME (6 ml). 25 Pd(PPh3)4 (15 mg, 0.15 mmol) and saturated Na2CO3 (0.95 ml) were added and the reaction was heated to 90 0 C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HTPLC (MeCN:H20:0.1% TFA) to yield desired products. Products were analyzed by LC-MS. 30 [0232] General synthetic scheme for BA112, BA115, BA121, BA122, BA124, BA136, BA138. BA141, and BA144. A solution of boronic acid (2.5 equivalents) in EtOH (1.65 ml) was added to a solution of 1-cyclopentyl-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine 57 WO 2007/114926 PCT/US2007/008395 (BA80, 1 equivalent) in DME (6 ml). Pd(PPh3)4 (15 mg, 0.15 mmol) and saturated Na2C03 (0.95 ml) were added and the reaction was heated to 90*C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCi and CH2C12. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC 5 (MeCN:H20:0.1% TFA) to yield desired products. Products were analyzed by LC-MS. [02331 General synthetic scheme for BAI11, BA114, BA116, BA117, BA1 19, and BA120. A solution of boronic acid (2.5 equivalents) in EtOH (1.65 ml) was added to a solution of 3 iodo-1-methyl-IH-pyrazolo[3,4-d]pyrimidin-4-amine (BA109, 1 equivalent) in DME (6 ml). Pd(PPh3)4 (15 mg, 0.15 mmol) and saturated Na2CO3 (0.95 ml) were added and the reaction D was heated to 90'C under an argon atmosphere overnight. After cooling, the reaction was extracted with saturated NaCl and CH2C12. Organic phases were combined, concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield desired products. Products were analyzed by LC-MS. [0234] Synthesis of 6-(4-amino-1-isopropyl-lH-pyrazolo[3,4-d]pyrimidin-3-yl)quinolin-2 5 amine (BA146). 3-(2-chloroquinolin-6-yl)-1-isopropyl-1H-pyrazolo[3,4-d]pyrinidin-4 amine (BA130, 50 mg, 0.15 mmol), acetamide (174 mg, 3.0 mmol) and K2C03 (104 mg, 0.75 mmol) were combined and heated to 200*C under an argon atmosphere for one hour. Reaction was cooled, then extracted with H20 and CH2Cl2. Organic phases were combined, concentrated in vacuo and purified by RP-HIPLC (MeCN:H20:0.1% TFA) to yield BA146 0 (22 mg, 46 % yield). ESI-MS (M+H)+ m/z calcd 320.2, found 320.4. [02351 Synthesis of 3-(3 -amino-1H-indazol-6-yl)-1 -isopropyl- 1H-pyrazolo[3,4 d]pyrimidin-4-amine (BA154). 4-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl) 2-fluorobenzonitrile (BA150, 20 mg, 0.07 mmol) was dissolved in n-BuOH (2 ml). Hydrazine monohydrate (0.400 ml) was added and the reaction was heated to 1 10*C under an 25 argon atomosphere and left stirring over night. Reaction mixture was concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA154 (15 mg, 70 % yield). ESI-MS (M+H)+ m/z calcd 309.2, found 309.4. [02361 Synthesis of 4-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-2 hydroxybenzonitrile (BA155_2). 4-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3 30 yl)-2-fluorobenzonitrile (BA150, 25 mg, 0.1 mmol) was dissolved in DMF (1 ml). t-BuOK (24 mg, 0.21 mmol) was added and the reaction was stirred at room temperature overnight. Reaction was then heated to 150*C for 24 hours. The reaction was then concentrated in 58 WO 2007/114926 PCT/US2007/008395 vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA1552 (21 mg, 89 % yield). ESI-MS (M+H)+ m/z calcd 295.1, found 295.4. [02371 Synthesis of 3-(3-aminobenzo[d]isoxazol-5-yl)-1-isopropyl-1H-pyrazolo[3,4 dlpyrimidin-4-amine (BA157__2) & 5-(4-amino-1-isopropyl-IH-pyrazolo[3,4-d]pyrimidin-3 i yl)-2-hydroxybenzonitrile (BA157_3). 5-(4-amino-1-isopropyl-IH-pyrazolo[3,4 d]pyrimidin-3-yl)-2-fluorobenzonitrile (BA151, 20 mg, 0.07 mmol) was dissolved in DMF (1 ml). t-BuOK (24 mg, 0.21 mmol) was added and the reaction was stirred at room temperature overnight. Reaction was then heated to 150*C for 24 hours. The reaction was then concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield ) BA1572 (7 mg), ESI-MS (M+H)+ m/z calcd 295.1, found 295.4 and BA1573 (8 mg), ESI MS (M+H)+ m/z calcd 310.1, found 310.4. [0238] Synthesis of 3-(3-amino- 1H-indazol-6-yl)-1 -isopropyl-1H-pyrazolo[3,4 d]pyrimidin-4-amine (BA159). 4-(4-anino-l-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl) 2,6-difluorobenzaldehyde (BA149, 20 mg, 0.063 mmol) was dissolved in n-BuOH (1 ml). 5 Hydrazine monohydrate (0.400 ml) was added and the reaction was heated to 100*C under an argon atomosphere and left stirring for 2.5 hours. Reaction mixture was concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA) to yield BA159 (15 mg, 77 % yield). ESI-MS (M+H)+ m/z calcd 312.1, found 312.4. [0239] Synthesis of 4-chloro-7-methyl-5-(naphthalen-2-yl)-7H-pyrrolo[2,3-d]pyrimidine D (ZK102). A solution of 4-chloro-5-iodo-7-methyl-7H-pyrrolo[2,3-d]pyrimidine (19 mg, 0.065 mmol), naphthalen-2-yl-2-boronic acid (12.2 mg, 0.071 mmol), Na 2

CO

3 (68.9 mg, 0.65 mmol) and PdCl 2 (dppf) (26.5 mg, 0.00325 mmol) in THF (3 mL) was heated to reflux overnight under an argon atmosphere. Reaction was concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA) to yield ZK102 (5 mg, 26% yield). ESI-MS (M+H)* m/z .5 calcd 294.1, found 294.3. [02401 Synthesis of 4-chloro-7-methyl-5-(3-biphenyl)-7H-pyrrolo[2,3-d]pyrimidine (ZK103). A solution of 4-chloro-5-iodo-7-methyl-7H-pyrrolo[2,3-d]pyrimidine (10 mg, 0.034 mmol), 3-biphenyl-boronic acid (7.4 mg, 0.038 mmol), Na 2

CO

3 (36.1 mg, 0.34 mmol) and PdCl 2 (dppf) (1.4 mg, 0.0017 mmol) in THF (10 mL) was heated to reflux ovemight 30 under an argon atmosphere. Reaction was concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA) to yield ZK103 (3 mg, 28% yield). ESI-MS (M+H)* m/z calcd 320.1, found 320.0. 59 WO 2007/114926 PCT/US2007/008395 [0241] Synthesis of 3-(4-tert-butylphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (ZK125). 1-tert-butyl-3-(4-tert-butylphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine was dissolved in a solution of formic acid (1 mL) and conc. HCI (0.1 mL) and heated to reflux for 2 hours. Reaction was concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA) to 5 yield ZK125 (quant.). ESI-MS (M+H)* m/z calcd 268.2, found 268.4. [0242] Synthesis of 3-(3-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (ZK126). 1-tert-butyl-3-(3-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (50 mg, 0.16 mmol) was dissolved in a solution of formic acid (5 mL) and conc. HC (0.1 mL) and heated to reflux for 2.5 hours. Reaction was concentrated in vacuo and purified by RP-HPLC ) (MeCN:H 2 0:0.1% TFA). ESI-MS (M+H)* m/z calcd 304.1, found 304.3. [0243] Synthesis of 3-m-tolyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (ZK127). 1-tert butyl-3-m-tolyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (23 mg, 0.1 mmol) was dissolved in a solution of formic acid (1 mL) and conc. HCl (0.3 mL) and heated to reflux for 2.5 hours. Reaction was concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA). 5 ESI-MS (M+H)* m/z calcd 226.1, found 226.3. [0244] Synthesis of 3-(3-nitrophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (ZK128). 1 tert-butyl-3-(3-nitrophenyl)-IH-pyrazolo[3,4-d]pyrimidin-4-amine (23 mg, 0.055 mmol) was dissolved in a solution of formic acid (5 mL) and conc. HCl (0.1 mL) and heated to reflux for 2 hours. Reaction was concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% D TFA). ESI-MS (M+H)* m/z calcd 257.1, found 257.3. [0245] Synthesis of 3-(benzo[d][1,3]dioxol-6-yl)-lH-pyrazolo[3,4-d]pyrimidin-4-amine (ZK129). 1-tert-butyl-3-(benzo[d][1,3]dioxol-6-yl)-I1H-pyrazolo[3,4-d]pyrimidin-4-anine (21 mg, 0.082 mmol) was dissolved in a solution of formic acid (1 mL) and conc. HCI (0.2 mL) and heated to reflux for 2 hours. Reaction was concentrated in vacuo and purified by .5 RP-HPLC (MeCN:H 2 0:0.1% TFA). ESI-MS (M+H)* m/z calcd 256.1, found 256.3. [0246] Synthesis of 3-(4-nitrophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (ZK130). 1 tert-butyl-3-(4-nitrophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (21 mg, 0.082 mmol) was dissolved in a solution of formic acid (2 mL) and conc. HCl (0.2 mL) and heated to reflux for 30 min. Reaction was concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% 50 TFA). ESI-MS (M+H)* m/z calcd 257.1, found 257.3. 60 WO 2007/114926 PCT/US2007/008395 [0247] Synthesis of 3-(3-(2,6-dichlorobenzyloxy)phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4 amine (ZK131). 1-tert-butyl-3-(3-(2,6-dichlorobenzyloxy)phenyl)-1H-pyrazolo[3,4 d]pyrimidin-4-amine (19.5 mg, 0.05 mmol) was dissolved in a solution of formic acid (2 mL) and conc. HCl (0.2 mL) and heated to reflux for 30 min. Reaction was concentrated in vacuo 5 and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA). ESI-MS (M+H)* m/z calcd 386.1, found 386.2. [02481 Synthesis of 3-(2,3-dimethylphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (ZK132). 1-tert-butyl-3-(2,3-dimethylphenyl)-lH-pyrazolo[3,4-d]pyrimidin-4-amine (34 mg, 0.14 mmol) was dissolved in a solution of formic acid (2 mL) and conc. HCI (0.2 mL) 3 and heated to reflux for 30 min. Reaction was concentrated in vacuo and purified by RP HPLC (MeCN:H 2 0:0.1% TFA). ESI-MS (M+H)* m/z calcd 240.1, found 240.4. [02491 Synthesis of 2-(4-amino-1H-pyrazolo[3,4-d]pyrimidin-3-yl)phenol (ZK133). 1 tert-butyl-2-(4-amino-1H-pyrazolo[3,4-d]pyrimidin-3-yl)phenol (5 mg, 0.014 mmol) was dissolved in a solution of formic acid (2 mL) and conc. HC1 (0.2 mL) and heated to reflux for 5 30 min. Reaction was concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA). ESI-MS (M+H)* m/z calcd 228.1, found 228.3. [0250] Synthesis of 3-o-tolyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (ZK134). 1-tert butyl-3-o-tolyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine was dissolved in a solution of formic acid (2 mL) and conc. HC1 (0.2 mL) and heated to reflux for 30 min. Reaction was 0 concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA). ESI-MS (M+H) m/z calcd 226.1, found 226.3. [02511 Synthesis of 3-(3-aminophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (ZK135). 1 tert-butyl-3-(3-aminophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine was dissolved in a solution of formic acid (2 mL) and conc. HCl (0.2 mL) and heated to reflux for 30 min. 25 Reaction was concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA). ESI-MS (M+H)* m/z calcd 227.1, found 227.3. [02521 Synthesis of 3-(3-(benzyloxy)phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (ZK136). 1-tert-butyl-3-(3-(benzyloxy)phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (19 mg, 0.052 mmol) was dissolved in a solution of formic acid (1 mL) and conc. HCl (0.1 mL) 30 and heated to reflux for 30 min. Reaction yielded a mixture of ZK136 and 3-(4-amino-1H pyrazolo[3,4-d]pyrimidin-3-yl)phenol (ZK138). Reaction was concentrated in vacuo and the 61 WO 2007/114926 PCT/US2007/008395 products purified by RP-HPLC (MeCN:H 2 0:0.1% TFA). ZK136: ESI-MS (M+H)* m/z calcd 318.1, found 318.3. ZK138: ESI-MS (M+H)* m/z calcd 228.1, found 228.3. [0253] Synthesis of 3-(4-aminophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (ZK137). 1 tert-butyl-3-(4-aminophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (9 mg, 0.032 mmol) was dissolved in a solution of formic acid (1 mL) and conc. HCl (0.2 mL) and heated to reflux. The reaction was allowed to proceed 30 min., then concentrated in vacuo and the products purified by RP-HPLC (MeCN:H 2 0:0.1% TFA). ESI-MS (M+H)* m/z calcd 227.1, found 227.3. . [02541 Synthesis of 3-(1,2,3,4-tetrahydronaphthalen-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-4 amine (ZK139). 1-tert-butyl-3-(1,2,3,4-tetrahydronaphthalen-2-yl)-1H-pyrazolo[3,4 d]pyrimidin-4-amine (9 mg, 0.029 mmol) was dissolved in a solution of formic acid (1 mL) and conc. HCl (0.1 mL) and heated to reflux. The reaction was allowed to proceed 30 min., then concentrated in vacuo and the products purified by RP-HPLC (MeCN:H 2 0:0.1% TFA). ESI-MS (M+H)* m/z calcd 266.1, found 266.4. 5 [0255] Synthesis of 5-iodo-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (ZK140). 4 chloro-5-iodo-7-methyl-7H-pyrrolo[2,3-d]pyrimidine (90 mg, 0.31 mmol) was taken up in 7N NH 3 /MeOH and heated in a sealed tube at 110* C overnight. Reaction was concentrated in vacuo to give a brown/off-white solid. [02561 Synthesis of 3-p-tolyl-1H-pyrazolo[3,4d]pyrimidin-4-amine (ZK141). 1-tert 3 butyl-3-p-tolyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine was dissolved in a solution of formic acid (1 mL) and conc. HCI (0.1 mL) and heated to reflux. The reaction was allowed to proceed 30 min., then concentrated in vacuo and the products purified by RP-HPLC (MeCN:H 2 0:0.1% TFA). ESI-MS (M+H)* m/z calcd 226.1, found 226.3. [0257] Synthesis of 3-(4-biphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (ZK142). 1-tert 5 butyl-3-(4-biphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (22 mg, 0.066 mmol) was dissolved in a solution of formic acid (1 mL) and conc. HC1 (0.1 nL) and heated to reflux. The reaction was allowed to proceed 30 min., then concentrated in vacuo and the products purified by RP-HPLC (MeCN:H 2 0:0.1% TFA). ESI-MS (M+H)* m/z calcd 288.1, found 288.3. 0 [0258] Synthesis of 3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (ZK143). 1-tert-butyl-3-(4-phenoxyphenyl)-lH-pyrazolo[3,4-d]pyrimidin-4-amine (19 mg, 54.1 mmol) 62 WO 2007/114926 PCT/US2007/008395 was dissolved in a solution of formic acid (1 mL) and conc. HCI (0.1 mL) and heated to reflux. The reaction was allowed to proceed 30 min., then concentrated in vacuo and the products purified by RP-HPLC (MeCN:H 2 0:0.1% TFA). ESI-MS (M+H)* m/z calcd 304.1, found 304.3. i [02591 Synthesis of 1-benzyl-3-(naphthalen-2-yl)-1H-pyrazolo[3,4-dIpyrimidin-4-amine (ZK147). 3-(naphthalen-2-yl)-1H-pyrazolo[3,4-d]pyimidin-4-amine (110 mg, 0.42 mmol) was dissolved in DMF (2 mL) and K 2 C0 3 (220 mg, 1.6 mmol) and benzyl bromide (71.8 mg, 0.42 mmol) were added. The reaction was heated to 600 C overnight, then cooled to RT and poured into water (30 mL). The precipitate was collected by filtration and then purified ) further by silica gel chromatography (5% MeOH/CH2Cl 2 ) to yield a white solid. [0260] Synthesis of 5-(4-(benzyloxy)pheny1)-7-methyl-7H-pyrrolo[2,3-d]pyrimidin- 4 amine (ZK150). A solution of 5-iodo-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (5 mg, 0.0 18 mmol), 4-(benzyloxy)phenylboronic acid (21 mg, 0.091 mmol), K 3 P0 4 (19.3 mg, 0.091 mmol) and Pd(PPh 3

)

4 (12.5 mg, 0.011 mmol) in DMF (3 mL) was heated to 60* C under an 5 argon atmosphere. Reaction was concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA). ESI-MS (M+H)* m/z calcd 331.1, found 331.3. [02611 Synthesis of 5-(3-bipheny1)-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (ZK151). A solution of 5-iodo-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (5 mg, 0.018 mmol), 3-biphenylboronic acid (18 mg, 0.091 mmol), K 3 P0 4 (19.3 mg, 0.091 mmol) and 0 Pd(PPh 3

)

4 (12.5 mg, 0.011 mmol) in DMF (3 mL) was heated to 60* C under an argon atmosphere. Reaction was concentrated in vacuo and purified by RP-HPLC (MeCN:H20:0.1% TFA). ESI-MS (M+H)"* m/z called 301.1, found 301.3. [0262] Synthesis of 5-(benzo[b]thiophen-2-yl)-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-4 amine (ZK152). A solution of 5-iodo-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (5 mg, 25 0.018 mmol), benzo[b]thiophen-2-yl-2-boronic acid (16 mg, 0.091 mmol), K 3

PO

4 (19.3 mg, 0.091 mmol) and Pd(PPh 3

)

4 (12.5 mg, 0.011 mmol) in DMF (3 mL) was heated to 600 C under an argon atmosphere. Reaction was concentrated in vacuo and purified by RP-HPLC (MeCN:H 2 0:0.1% TFA). ESI-MS (M+H)* m/z calcd 281.1, found 281.3. [0263] Synthesis of 3-(naphthalen-2-yl)-1-phenethyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine 30 (ZK155). 2-(methoxy(naphthalen-6-yl)methylene)malononitrile (100 mg, 0.43 mmol) and phenethylhydrazine hydrogen chloride (58.5 mg, 0.43 mmol) were dissolved in EtOH (3 mL) 63 WO 2007/114926 PCT/US2007/008395 and TEA (60 iL, 0.43 mmol) and heat to reflux for one hour. The product was extracted with diethylether and concentrated in vacuo. This concentrate was then dissolved in formamide (10 mL) and heated to 160-180* C overnight. The following day the reaction was cooled, poured into water, and the precipitated product collected by filtration. ESI-MS 5 (M+H)* m/z called 366.2, found 366.2. [02641 Synthesis of 1-isopropyl-3-(naphthalen-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (ZK156). 2-(methoxy(naphthalen-6-y)methylene)malononitrile (100 mg, 0.43 mmol) and isopropylhydrazine hydrogen chloride (47.3 mg, 0.43 mmol) were dissolved in EtOH (3 mL) and TEA (1 eq.) and heat to reflux for one hour. The product was extracted with diethylether 3 and concentrated in vacuo. This concentrate was then dissolved in formamide (10 mL) and heated to 160-180" C overnight. The following day the reaction was cooled, poured into water, and the precipitated product collected by filtration. ESI-MS (M+H)* m/z calcd 304.2, found 304.2. [0265] Synthesis of 1-ethyl-3-(naphthalen-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine 5 (ZK157). 3-(naphthalen-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (100 mg, 0.42 mmol) was dissolved in DMF (3 mL) and K 2 C0 3 (220 mg, 1.6 mmol) and ethyl iodide (37 piL, 0.46 mmol) were added. The reaction was heated to 60" C overnight, then cooled to RT and poured into water (30 mL). The precipitate was collected by filtration. ESI-MS (M+H)* m/z calcd 290.1, found 290.2. 0 [02661 Synthesis of 1-cyclopentyl-3-(naphthalen-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-4 amine (ZK158). 3-(naphthalen-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (100 mg, 0.42 mmol) was dissolved in DMF (3 mL) and K 2 C0 3 (220 mg, 1.6 mmol) and cyclopentyl bromide (49.5 tL, 0.46 mmol) were added. The reaction was heated to 600 C overnight, then cooled to RT and poured into water (30 mL). The precipitate was collected by filtration. .5 ESI-MS (M+H)* m/z calcd 330.2, found 330.2. [0267] Synthesis of 1-allyl-3-(naphthalen-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (ZK159). 3-(naphthalen-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (50 mg, 0.21 mmol) was dissolved in DMF (1.5 mL) and K 2 C0 3 (110 mg, 0.8 mmol) and allyl iodide (23 pL, 0.25 mmol) were added. The reaction was heated to 60" C overnight, then cooled to RT and 30 poured into water (30 mL). The precipitate was collected by filtration. ESI-MS (M+H) m/z calcd 302.1, found 302.2. 64 WO 2007/114926 PCT/US2007/008395 [0268] Synthesis of 2-(4-anino-3-(naphthalen-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-1 yl)acetamide (ZK162). 3-(naphthalen-2-yl)-H-pyrazolo[3,4-d]pyrimidin-4-amine (50 mg, 0.21 mmol) was dissolved in DMF (1.5 mL) and K 2 C0 3 (110 mg, 0.8 mmol) and iodoacetamide (46 mg, 0.25 mmol) were added. The reaction was heated to 60* C overnight, i then cooled to RT and poured into water (30 mL). The precipitate was collected by filtration. ESI-MS (M+H)* m/z called 319.1, found 319.2. [0269] Synthesis of 1-(cyclopropylmethyl)-3-(naphthalen-2-yl)-1H-pyrazolo[ 3

,

4 d]pyrimidin-4-amine (ZK165). 3-(naphthalen-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amrine (50 mg, 0.21 mmol) was dissolved in DMF (1.5 mL) and K 2 C0 3 (110 mg, 0.8 mmol) and ) cyclopropyl methyl bromide (22 tL, 0.25 mmol) were added. The reaction was heated to 600 C overnight, then cooled to RT and poured into water (30 mL). The precipitate was collected by filtration. ESI-MS (M+H)* m/z calcd 316.2, found 316.2. [02701 Synthesis of 1-isopentyl-3-(naphthalen-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (ZK161). 3-(naphthalen-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (50 mg, 0.21 mmol) 5 was dissolved in DMF (1.5 mL) and K 2 C0 3 (110 mg, 0.8 mmol) and isobutyl bromide were added. The reaction was heated to 60* C overnight, then cooled-to RT and poured into water (30 mL). The precipitate was collected by filtration. ESI-MS (M+H)* m/z calcd 332.2, found 332.3. [02711 Synthesis of 3-(naphthalen-2-yl)-1-((E)-3-phenylprop-1-enyl)-1H-pyrazolo[3,4 D d]pyrimidin-4-amine (ZK167). 3-(naphthalen-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (50 mg, 0.21 mmol) was dissolved in DMF (1.5 mL) and K 2 C0 3 (110 mg, 0.8 mmol) and 1 ((E)-3-bromoprop-1-enyl)benzene were added. The reaction was heated to 60* C overnight, then cooled to RT and poured into water (30 mL). The precipitate was collected by filtration. ESI-MS (M+H)* m/z calcd 378.2, found 378.2. ?5 [0272] Synthesis of 3-(naphthalen-2-yl)-1-(prop-2-ynyl)-1H-pyrazolo[3,4-d]pyrimidin-4 amine (ZK168). 3-(naphthalen-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (50 mg, 0.21 rnmol) was dissolved in DMF (1.5 mL) and K 2 C0 3 (110 mg, 0.8 mmol) and propargyibromide were added. The reaction was heated to 60" C overnight, then cooled to RT and poured into water (30 mL). The precipitate was collected by filtration. ESI-MS 30 (M+H)* m/z calcd 300.1, found 300.2 65 WO 2007/114926 PCT/US2007/008395 [02731 Synthesis of 3-ethoxy-4-methoxybenzoyl chloride (ZK299). 3-ethoxy-4 methoxybenzoic acid (5 g, 25.5 mmol) was added to a solution of CH 2 Cl 2 (40 mL) and benzene (20 mL) in a flame-dried 150 mL round bottom flask. Anhydrous DMF (9 drops) was added and the solution was cooled on ice. Oxalyl chloride (11 mL, 128 mmol) was 5 added dropwise, and the reaction was then allowed to warm to RT. The reaction was stirred at RT for 90 minutes, then concentrated in vacuo yield an off-white solid. The solid was placed on a high-vacuum line for 2 hours, and then taken onto the next step without further characterization. [02741 Synthesis of 2-((3-ethoxy-4-methoxyphenyl)(hydroxy)methylene)malononitrile 0 (ZK301). NaH (2.2 g, 56 mmol, 60% dispersion in paraffin oil) was added to a solution of malononitrile (1.85 g, 28 mmol) in THF (30 mL) on ice. 3-ethoxy-4-methoxybenzoyl chloride (25.5 mmol) was dissolved in THF (50 mL) and added the first solution dropwise by syringe at 0* C. The ice was then removed and the reaction was allowed to proceed at RT for 60 min. IN HCl (100 mL) was added and the solution was extracted three times with EtOAc. 5 The organic phase was dried with MgS04, filtered, and concentrated in vacuo to give an orange solid that was taken onto the next step without further characterization. [02751 Synthesis of 2-((3-ethoxy-4-methoxyphenyl)(methoxy)methylene)malononitrile (ZK302). 2-((3-ethoxy-4-methoxyphenyl)(hydroxy)methylene)malononitrile (25.5 mmol) and sodium bicarbonate (17 g, 204 mmol) were combined in a solution of 1,4-dioxane (48 0 mL) and water (8 mL). Dimethylsulphate (17 mL, 178 mmol) was slowly added and the reaction was heated to 80-90* C for 2 hours. The reaction was cooled to RT, water was added, and the aqueous phase extracted three times with EtOAc (200 mL). The organic phases were combined, dried with MgSO 4 , and filtered to give a red oil. The oil was purified by silica gel chromatography (10% EtOAc/Hexanes, Rr- 0.1) to give a white solid (3.59 g, 25 54.5% yield over three steps). ESI-MS (M+H)* m/z calcd 259.1, found 259.0. [0276] Synthesis of 5-amino-3-(3-ethoxy-4-methoxyphenyl)-1-isopropyl-lH-pyrazole-4 carbonitrile (ZK303). 2-((3-ethoxy-4-methoxyphenyl)(methoxy)methylene)malononitrile (200 mg, 0.78 mmol), isopropylhydrazine hydrogen chloride (86 mg, 0.78 mmol), and triethylamine (o.10 mL, 0.78 mmol) were combined in ethanol (5 mL) and heated to reflux 30 for 90 minutes. The reaction was then cooled to RT, water was added and the aqueous phase was extracted three times with EtOAc. The organic phase was concentrated and carried onto the next step without further characterization. ESI-MS (M+H)* m/z calcd 301.1, found 301.0 66 WO 2007/114926 PCT/US2007/008395 [02771 Synthesis of 3-(3-ethoxy-4-methoxyphenyl)-1-isopropyl-1H-pyrazolo[3,4 d]pyrimidin-4-amine (ZK305). 5-amino-3-(3-ethoxy-4-methoxyphenyl)-1-isopropyl-IH pyrazole-4-carbonitrile was dissolved in formamide (20 mL) and heated to 180* C overnight. The next day the reaction was cooled to RT, water was added, and the precipitate was collected by filtration. The precipitate was then dissolved in CH 2 C1 2 /MeOH and passed through a silica plug. The product was then lyophilized from benzene to yield an off-white solid (48 mg, 19% over two steps). ESI-MS (M+H)* m/z calcd 328.2, found 328.0. [0278] Synthesis of 5-amino-3-(3-ethoxy-4-methoxyphenyl)-l-(2-hydroxyethyl)-1H pyrazole-4-carbonitrile (ZK304). 2-((3-ethoxy-4 ) methoxyphenyl)(methoxy)methylene)malononitrile (200 mg, 0.78 mmol), 2 hydroxyethylhydrazine (0.056 mL, 0.78 mmol), and triethylamine (0.10 mL, 0.78 mmol) were combined in ethanol (5 mL) and heated to reflux for 90 minutes. The reaction was then cooled to RT, water was added and the aqueous phase was extracted three times with EtOAc,

CH

2 Cl 2 , and CHC 3 . The organic phase was concentrated and carried onto the next step 5 without further characterization. ESI-MS (M+H)* m/z calcd 303.1, found 303.0. [0279] 2-(4-amino-3-(3-ethoxy-4-methoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1 yl)ethanol (ZK306). 5-amino-3-(3-ethoxy-4-methoxyphenyl)-1-(2-hydroxyethyl)-lH pyrazole-4-carbonitrile was dissolved in formamide (20 mL) and heated to 180* C overnight. The next day the reaction was cooled to RT, water was added, and the precipitate was D collected by filtration. The precipitate was then dissolved in CH 2 Cl 2 /MeOH and passed through a silica plug. The product was then lyophilized from benzene to yield a brown solid (6.4 mg, 2.5% over two steps). ESI-MS (M+H)* m/z calcd 330.1, found 330.0. B. Structural Studies [02801 Crystal structures of p110y have been reported, alone and in complex with ATP or !5 pan-specific inhibitors such as LY294002 and wortmannin (Walker et al., 2000; Walker et al., 1999). To explore how potent and selective inhibitors bind, the crystal structures of P13 K inhibitors from three chemotypes bound to human p1 10 y were determined at 2.5 - 2.6 A resolution: the quinazoline purine PIK-39, the imidazopyridine PIK-90 and the phenylthiazole PIK-93 (Figure 2). 3O [0281] Based on these co-crystal structures and a conserved arylmorpholine pharmacophore model, structural models were generated for three additional chemotypes 67 WO 2007/114926 PCT/US2007/008395 bound to p11Oy: the pyridinylfuranopyrimidine PI-103, the morpholinochromone PIK-108, and the morpholinopyranone KU-55933 (Figure 2). Model-building for these inhibitors was guided by the observation that each compound contains the key arylmorpholine pharmacophore found in LY294002. [02821 - PIK-39 is an isoquinoline purine that inhibits pl106 at mid-nanomolar concentrations, p11 Oy and p110 at concentrations ~100-fold higher, and shows no activity against any other P13-K family member, including p11 Oct, at concentrations up to 100 pM (Figure 5). The biochemical selectivity of this compound is achieved through an unusual binding mode revealed in its co-crystal structure with p1 10y (Figure 2C). Only the ) mercaptopurine moiety of PIK-39 makes contacts within the interior of the ATP binding pocket, and this ring system is rotated ~110" and twisted ~35* out of the plane relative to the adenine of the ATP. In this orientation, it satisfies hydrogen bonds to the backbone amides of Val 882 and Glu 880 (thereby recapitulating the hydrogen bonds made by N1 and N6 of adenine). 5 [02831 In contrast to other P13-K inhibitor structures, PIK-39 does not access the deeper pocket in the active site interior (Figure 2C, lightly shaded area labeled as "Affinity Pocket"). Instead, the aryl-isoquinoline moiety of PIK-39 extends out to the entrance of the ATP binding pocket (Figure 2B). In this region, the kinase accommodates the inhibitor by undergoing a conformational rearrangement in which Met 804 shifts from an "up"' position, 0 in which it forms the ceiling of the ATP binding pocket, to a "down" position which it packs against the isoquinoline moiety. The effect of this movement, which is unique to the PIK-39 structure (Figure 2B), is to create a novel hydrophobic pocket between Met 804 and Trp 812 at the entrance to the ATP binding site. This induced-fit pocket buries -180 A2 of solvent accessible inhibitor surface area, enabling PIK-39 to achieve nanomolar affinity despite Z5 limited contacts within tle active site core. [02841 Co-crystal structures of PIK-90 and PIK-93 compounds bound to pIOy were determined. PIK-90 and PIK-93 both make a hydrogen bond to the backbone amide nitrogen of Val 882 (Figure 2D), an interaction conserved among all known P13-K inhibitors (Walker et al., 2000). In addition to this hydrogen bond, PIK-93 makes a second hydrogen bond to 30 the backbone carbonyl of Val 882 and a third between its sulphonamide moiety and the side chain of Asp 964. PIK-93 is one of the most polar inhibitors in our panel (clogP = 1.69) and these extended polar interactions may compensate for its limited hydrophobic surface area. 68 WO 2007/114926 PCT/US2007/008395 [02851 PIK-90 binds in a mode similar to PIK-93, although this larger compound makes more extensive hydrophobic interactions, burying 327 A 2 of solvent accessible surface area. To achieve this, PIK-90 projects its pyridine ring into a deeper cavity that is partially accessed by PIK-93 but not occupied by ATP (Figure 2D, lightly shaded circle). In this region, the pyridine ring of PIK-90 is poised to make a hydrogen bond to Lys 833, and we find that replacement of this pyridine nitrogen with carbon results in a 100-fold loss in affinity (PIK-95, Figure 4). PI-103, a third multi-targeted P13K inhibitor, projects a phenol into the same pocket based on an arylmorpholine pharmacophore model (Figure 2D). [0286] Two structural features distinguish these potent, multi-targeted inhibitors from the ) more selective compounds in our panel. First, these compounds adopt a flat conformation in the ATP binding pocket, whereas highly selective inhibitors project out of the plane occupied by ATP (Figure 2). Second, the most potent inhibitors project into a deeper binding pocket that is not accessed by ATP (Figure 2A). Much of the surface of this affinity pocket is contributed by the side-chain of Ile 879. 5 [02871 The mercaptopurine in the PIK-39 structure was replaced with adenine to yield a model of IC87114 (Figure 3A). This substitution provided the adenine of IC87114 in the correct orientation to make the same hydrogen bonds as the mercaptopurine of PIK-39, even though these two ring systems are rotated by 110* with respect to each other. [02881 Unlike other inhibitor chemotypes, PIK-39 does not exploit the P13-kinase affinity D pocket (Figure 2C). The pyrazolopyrimidine analog of IC87114 (PIK-293) as well as a novel analog containing an m-phenol (PIK-294, Figure 3A) were then tested for inhibition of the class I P13-Ks. PIK-294 was up to 60-fold more potent than PIK-293 (Figure 3A). [02891 The structure of PIK-39 bound to p1lOy reveals a conformational rearrangement of Met 804 that creates an induced pocket, and we have hypothesized that this conformational 25 rearrangement underlies the selectivity of PIK-39 for p1108. A prediction of this model is that mutation of Met 804 should perturb the binding of pl 106-selective inhibitors (which access the induced pocket), but not affect other classes of inhibitors (which do not access this pocket). Modeling suggests that mutation of Met 804 to a p-branched amino acid (such as valine or isoleucine) should restrict the pocket formed by rearrangement of that residue 30 (Figure 3B, right). Therefore, we mutated the corresponding residue in p1108 (Met 752) to valine or isoleucine, expressed and purified these kinases, and tested them for sensitivity to 69 WO 2007/114926 PCT/US2007/008395 P13-K inhibitors (Figure 3B). We find that M7521 and M752V p1 10< are resistant to the p1108-selective inhibitors PIK-39 and IC87114, but retain sensitivity to the p1lOc/multi targeted inhibitors PIK-90, PIK 93, and PI-103. This chemotype-specific resistance supports the unique role of Met 752 in gating an inducible selectivity pocket. [02901 Antagonist modeling was performed using the PyMOL Molecular Graphics System. All p11 Oy crystal structures (PDB codes in parentheses), including the Apo (1E8Y), ATP (1E8X), Wortmannin (1E7U), LY294002 (1E7V), Quercetin (1E8W), Myricetin (1E90), and Staurosporine (lE8Z), PIK-90, PIK-93, and PIK-39 bound forms were structurally aligned using PyMOL's align function. Models for the inhibitors PIK-108, KU-55933, and PI-103 were built on top of the LY294002 arylmorpholine scaffold (1E7V) using PyMOL's fragment building function. A model for the inhibitor IC87114 was similarly built on top of the PIK 39 aryl-isoquinoline scaffold. [0291] The model for PI-103 was built into the protein structure of pll0y bound to PIK-90, because the PIK-90 structure contains the enlarged affinity pocket that is necessary to 5 accommodate P]X-103's phenolic moiety (the PIK-90 p11 Oy structure otherwise does not exhibit any conformational differences in the arymorpholine-binding region in comparison to the LY294002-bound plOy structure). The models for PIK-108, KU-55933, and IC87114 were built into the protein structure of p 11Oy bound to PIK-39 because these inhibitors possess bulky groups that project out of the adenine plane and are likely to exploit the unique ) "Met 804 down" induced-fit pocket. In all inhibitor models, the choice of protein structure and inhibitor binding mode is based on extensive biochemical SAR as well as inhibitor geometry. The protein structures and inhibitor models have not been minimized to optimize binding energy, but care was taken to prevent any gross steric clashes and to satisfy key hydrogen bonds. :5 C. pll0a/p85a, p1100/p85a, p110S/p85a, and p110y Assay [0292] The class I P13-Ks were either purchased (p1 10oa/p85a, p110p/p85a, p11O8/p85aC from Upstate, and p11 Oy from Sigma) or expressed as previously described (Knight et al., 2004). IC50 values were measured using either a standard TLC assay for lipid kinase activity (described below) or a high-throughput membrane capture assay. Kinase reactions were 50 performed by preparing a reaction mixture containing kinase, inhibitor (2% DMSO final concentration), buffer (25 mM HEPES, pH 7.4, 10 mM MgC12), and freshly sonicated 70 WO 2007/114926 PCT/US2007/008395 phosphatidylinositol (100 ptg/ml). Reactions were initiated by the addition of ATP containing 10 ptCi of y-32P-ATP to a final concentration 10 or 100 pM, as indicated in Figure 5, and allowed to proceed for 5 minutes at room temperature. For TLC analysis, reactions were then terminated by the addition of 105 p1 1N HC1 followed by 160 pl CHC13:MeOH (1:1). The i biphasic mixture was vortexed, briefly centrifuged, and the organic phase transferred to a new tube using a gel loading pipette tip precoated with CHC1 3 . This extract was spotted on TLC plates and developed for 3 - 4 hours in a 65:35 solution of n-propanol:1M acetic acid. The TLC plates were then dried, exposed to a phosphorimager screen (Storm, Amersham), and quantitated. For each compound, kinase activity was measured at 10 - 12 inhibitor ) concentrations representing two-fold dilutions from the highest concentration tested (typically, 200 pM). For compounds showing significant activity, IC50 determinations were repeated two to four times, and the reported value is the average of these independent measurements. [0293] Results are set forth below in Table 2. 5 D. AbI Assay [02941 Inhibitors (final concentration: 10 pM) were assayed in triplicate against recombinant full-length Abl or Abl (T3151) (Upstate) in an assay containing 25 mM HEPES, pH 7.4, 10 mM MgC12, 200 PM ATP (2.5 pCi of y-32P-ATP), and 0.5 mg/mL BSA. The optimized Abl peptide substrate EAIYAAPFAKKK was used as phosphoacceptor (200 iM) . 0 Reactions were terminated by spotting onto phosphocellulose sheets, which were washed with 0.5% phosphoric acid (approximately 6 times, 5-10 minutes each). Sheets were dried and the transferred radioactivity quantitated by phosphorimaging. [0295] Results are set forth below in Table 3. E. Hck Assay 25 [02961 HEck: Inhibitors (final concentration: 10 pM) were assayed in triplicate against recombinant full-length Hck in an assay containing 25 mM HEPES, pH 7.4, 10 mM MgC12, 200 pM ATP (2.5 piCi of y-32P-ATP), and 0.5 mg/mL BSA. The optimized Src family kinase peptide substrate EIYGEFKKK was used as phosphoacceptor (200 gM) . Reactions were terminated by spotting onto phosphocellulose sheets, which were washed with 0.5% 71 WO 2007/114926 PCT/US2007/008395 phosphoric acid (approximately 6 times, 5-10 minutes each). Sheets were dried and the transferred radioactivity quantitated by phosphorimaging. [0297] Results are set forth below in Table 3. F. Inulsin Receptor (IR) Assay [0298] Ilnhibitors (final concentration: 10 pM) were assayed in triplicate against recombinant insulin receptor kinase domain (Upstate) in an assay containing 25 mM HEPES, pH 7.4, 10 mM MgC12, 10 mM MnC12, 200 pM ATP (2.5 gCi of y-32P-ATP), and 0.5 mg/mL BSA. Poly E-Y (Sigma; 2 mg/mL) was used as a substrate. Reactions were terminated by spotting onto nitrocellulose, which was washed with 1M NaCl% phosphoric acid (approximately 6 times, 5-10 minutes each). Sheets were dried and the transferred radioactivity quantitated by phosphorimaging. [0299] Results are set forth below in Table 4. G. Src Assay [0300] Src, Src (T3381): Inhibitors (final concentration: 10 pM) were assayed in triplicate 5 against recombinant full-length Src or Src (T3381) in an assay containing 25 mM HEPES, pH 7.4, 10 mM MgC12, 200 pM ATP (2.5 pCi of y-32P-ATP), and 0.5 mg/mL BSA. The optimized Src family kinase peptide substrate EIYGEFKKK was used as phosphoacceptor (200 pM) . Reactions were terminated by spotting onto phosphocellulose sheets, which were washed with 0.5% phosphoric acid (approximately 6 times, 5-10 minutes each). Sheets were .0 dried and the transferred radioactivity quantitated by phosphorimaging. [0301] Results are set forth below in Table 3. H. DNA-PK (DNAK) Assay [0302] DNA-PK was purchased from Promega and assayed using the DNA-PK Assay System (Promega) according to the manufacturer's instructions. 25 [0303] Results are shownin Table 2. 72 WO 2007/114926 PCT/US2007/008395 I. mTOR Assay Inhibitors (final concentrations 50 pM -0.003 pM) were tested against recombinant mTOR (Invitrogen) in an assay containing 50 mM HEPES, pH 7.5, 1mM EGTA, 10 mM MgCl2, 2.5 mM, 0.01% Tween, 10 p.M ATP (2.5 pCi of [t-32P-ATP), and 3 tg/mL BSA. Rat i recombinant PHAS-1/4EBP1 (Calbiochem; 2 mg/mL) was used as a substrate. Reactions were terminated by spotting onto nitrocellulose, which was washed with 1M NaCl/1% phosphoric acid (approximately 6 times, 5-10 minutes each). Sheets were dried and the transferred radioactivity quantitated by phosphorimaging. [0304] Results are set forth in Table 4 below. ) J. Vascular endothelial growth receptor [0305] Vascular endothelial growth receptor 2(KDR): Inhibitors (final concentrations 50 pM -0.003 pM) were tested against recombinant KDR receptor kinase domain (Invitrogen) in an assay containing 25 mM HEPES, pH 7.4, 10 mM MgCl2, 0.1% BME, 10 PM ATP (2.5 p.Ci of R-32P-ATP), and 3 pg/mL BSA. Poly E-Y (Sigma; 2 mg/mL) was used as a 5 substrate. Reactions were terminated by spotting onto nitrocellulose, which was washed with 1M NaCl/1% phosphoric acid (approximately 6 times, 5-10 minutes each). Sheets were dried and the transferred radioactivity quantitated by phosphorimaging. [03061 Results are set forth in Table 3 below. K. Ephrin receptor B4 (EphB4) Assay 20 [03071 Inhibitors (final concentrations 50 pM -0.003 pM) were tested against recombinant Ephrin receptor B4 kinase domain (Invitrogen) in an assay containing 25 mM HEPES, pH 7.4, 10 mM MgCl2, 0.1% BME, 10 p.M ATP (2.5 pCi of p-32P-ATP), and 3 pg/mL BSA. Poly E-Y (Sigma; 2 mg/mL) was used as a substrate. Reactions were terminated by spotting onto nitrocellulose, which. was washed with IM NaCl/1% phosphoric acid (approximately 6 25 times, 5-10 minutes each). Sheets were dried and the transferred radioactivity quantitated by phosphorimaging. 103081 Results are set forth in Table 3 below. 73 WO 2007/114926 PCT/US2007/008395 L. Epidermal growth factor receptor (EGFR) Assay Inhibitors (final concentrations 50 xM -0.003 pM) were tested against recombinant EGF receptor kinase domain (Invitrogen) in an assay containing 25 mM HEPES, pH 7.4, 10 mM MgC12, 0.1% BME, 10 pM ATP (2.5 pCi of p-32P-ATP), and 3 pg/mL BSA. Poly E-Y (Sigma; 2 mg/mL) was used as a substrate. Reactions were terminated by spotting onto nitrocellulose, which was washed with 1M NaC1/1% phosphoric acid (approximately 6 times, 5-10 minutes each). Sheets were dried and the transferred radioactivity quantitated by phosphorimaging. [0309] Results are set forth in Table 3 below. M. KIT Assay [0310] Inhibitors (final concentrations 50 pM -0.003 pM) were tested against recombinant KIT kinase domain (Invitrogen) in an assay containing 25 mM HEPES, pH 7.4, 10 mM MgCI2, 1mM DTT, 10mM MnCl2, 10 pM ATP (2.5 pCi of p-32P-ATP), and 3 pg/mL BSA. Poly E-Y (Sigma; 2 mg/mL) was used as a substrate. Reactions were terminated by spotting 5 onto nitrocellulose, which was washed with 1M NaCl/1% phosphoric acid (approximately 6 times, 5-10 minutes each). Sheets were dried and the transferred radioactivity quantitated by phosphorimaging. [0311] Results are set forth in Table 4 below. N. RET Assay Z0 [0312] Inhibitors (final concentrations 50 pM -0.003 pM) were tested against recombinant RET kinase domain (Invitrogen) in an assay containing 25 mM HEPES, pH 7.4, 10 mM MgCl2, 2.5mM DTT,10 pM ATP (2.5 pCi of p-32P-ATP), and 3 jig/mL BSA. The optimized AbI peptide substrate EAIYAAPFAKKK was used as phosphoacceptor (200 pM). Reactions were terminated by spotting onto phosphocellulose sheets, which were washed 25 with 0.5% phosphoric acid (approximately 6 times, 5-10 minutes each). Sheets were dried and the transferred radioactivity quantitated by phosphorimaging. [0313] Results are set forth in Table 4 below. 74 WO 2007/114926 PCT/US2007/008395 0. Platelet derived growth factor receptor (PDGFR) Assay [03141 Inhibitors (final concentrations 50 pM -0.003 pM) were tested against recombinant PDG receptor kinase domain (Invitrogen) in an assay containing 25 mM HEPES, pH 7.4, 10 mM MgC12, 2.5mM DTT,10 VM ATP (2.5 piCi of p-32P-ATP), and 3 pg/mL BSA. The optimized AbI peptide substrate EAIYAAPFAKKK was used as phosphoacceptor (200 ptM) . Reactions were terminated by spotting onto phosphocellulose sheets, which were washed with 0.5% phosphoric acid (approximately 6 times, 5-10 minutes each). Sheets were dried and the transferred radioactivity quantitated by phosphorimaging. [03151 Results are set forth in Table 4 below. ) P. FMS-related tyrosine kinase 3 (FLT-3) Assay [03161 Inhibitors (final concentrations 50 p.M -0.003 jiM) were tested against recombinant FLT-3 kinase domain (Invitrogen) in an assay containing 25 mM HEPES, pH 7.4, 10 mM MgCI2, 2.5mM DTT,10 pM ATP (2.5 Ci of p-32P-ATP), and 3 pig/mL BSA. The optimized Abl peptide substrate EAIYAAPFAKKK was used as phosphoacceptor (200 pM) . 5 Reactions were terminated by spotting onto phosphocellulose sheets, which were washed with 0.5% phosphoric acid (approximately 6 times, 5-10 minutes each). Sheets were dried and the transferred radioactivity quantitated by phosphorimaging. Results are set forth in Table 4 below. Q. TEK receptor tyrosine kinase (TIE2) Assay !0 [03171 Inhibitors (final concentrations 50 pM -0.003 pM) were tested against recombinant TIE2 kinase domain (Invitrogen) in an assay containing 25 mM HEPES, pH 7.4, 10 mM MgCl2, 2mM DTT, 10mM MnCl2, 10 pM ATP (2.5 p±Ci of p-32P-ATP), and 3 pg/mL BSA. Poly E-Y (Sigma; 2 mg/mL) was used as a substrate. Reactions were terminated by spotting onto nitrocellulose, which was washed with 1M NaCl/1% phosphoric acid (approximately 6 25 times, 5-10 minutes each). Sheets were dried and the transferred radioactivity quantitated by phosphorimaging. Results are set forth in Table 4 below. 75 WO 2007/114926 PCT/US2007/008395 R. Results 103181 In Table 1, the compounds have the formula:

R

3 6

R

2 N ~ K- X N N R (I). R1 and R 2 are as defined in Table 1. X is =N- except where indicated. R 3 6 is -NH 2 except where indicated. 76 WO 2007/114926 PCT/US2007/008395 Table 1 Cd RI R2 Cpd RI R2 cN KS167 -HNBA46 C ZK141 -H BA45 _C 0 ZKI 27 -H N" BA150 MK134 -H NBA151 ZK1 32 -H MeBA2I /74 ZK1 25 -H NBA52 IN BA56 _____ _______ BA53IN 0 ZKI 38 -H NBA31 _____ F KS287 XC=HCN BA152 _____ R ~~ &OH ___ KS288 N-ehl NBA149 _______ 77 WO 2007/114926 PCT/US2007/008395 Cpd RI R2 Cpd RI R2 0 KS284 BA32 OH BA60 Me BA55 O Me O ZK318 -H BA35 Me OH ZK320 -H BA34 / aOH N ZK333 -Me B38 Me N ZK323 OH BA40 Me ?l ZK327 BA41 OH BA77d F BA14 V- OH BA78d F BA12 FI CH BA22 BA30 0 F H F H 0 BA79d ZK149 -H |_O 78 WO 2007/114926 PCT/US2007/008395 Cpd RI R2 Cpd RI R2 Br BA85 O e ZK126 -H Br/ 9OH 0 BA87 OH ZK143 -H Br Z52-MeN ZK502 IO ZK150 X=CH Br OH OH ZK489 -Me ZK136 -H Br OH ZK487 ZK131 -H Br 0H -Me Zk491 ZK151 X=CH Br Zk493 OH_ ZK142 -H F dOH _ c BA62d ZK139 -H F ZK450 NH 2 FH KS207 -H ZK454 ,NH 2 OH KS208 -Me F-Me ZK469 NC OH ZK102 C is 79 WO 2007/114926 PCT/US2007/008395 Cpd RI R2 Cpd R1 R2 ZK471 CN _9_L ZK157 F ZK461 N ZK159 F ZK413 NH OH ZK156 F ZK379 N KS63 x F ZK421 NH ZK158 F ZK403 N OH ZK147 F ZK405 NH OH ZK155 F ZK432 ZK162

NH

2 F c ZK434 O OH ZK165 F ZK465 _0__1__OH ZK161 Fc 0 OH ZK377 HN F ZK167 F OH ____ ZK399 OH ZK168 ~ 80 WO 2007/114926 PCT/US2007/008395 Cd R1 R2 Cpd RI R2 ZK401 ( BA116 -MeEt _N~a )-,__,-OO F BA62 OMe BAI 7 CIN ZK358 OH BA 34 C ZK452 NH 2 OHBAI 05 C N_ L,_$-OH__ _ _ _ ZK456 NH 2 BA122 C I ZK463 BA111 -Me ZK371 '34 ./_ OH BA102 ZK409 L:NH OH BA112 CI OHN ZK428 C O O BA1 18 I NI N ZK430 O BA130 / ZK387 NH OH BA132 X 81 WO 2007/114926 PCT/US2007/008395 Cpd RI R2 Cpd R1 R2 NN OH N ZK389 H BA139 OH NH N OH_ __ _ __ _ _ ZK369 H BA158 0 H O CI)AN ZK385 HN BA140 HO Ni N Oc H_ _ ZK391 H BA141 NH2 CN N NH 2 -,OH BA155 2 O BA146 r OH HN'NH 2 NA ~CN BA157 2 CN BA142 OH O NH BA59 BA145 / OMeN BA63 FM BA147 _ NH 2 OH0 BA93 N F BA148 -Me 0 BA49 BA143 0 82 WO 2007/114926 PCT/US2007/008395 Cpd RI ' R2 Cpd R1 R2 BAI 5 BA144 0 OMe N ZK321 -H BA129 OMe N OH ZK337 -Me BA133 OMe ZK347 OH BA133 H OMe N OH ZK411 NH__ _ BA89 2H-M OMe N OH ZK349 BAI18 HI OMe N OH ZK423 BA121 H MeN OH0 ZK411 DN H >%BA89 _______________ OMeN NH OH ZK407 yH ~BA94 K/ OEt N OH _ BA98 ___ __BA135 X______ H N ' BA23 /BAl 37 , 83 WO 2007/114926 PCT/US2007/008395 Cpd R1 R2 Cpd R1 R2 Ox~e N N ZK485 BA138 N H OMe ZK495 HO N"~" 860

NNH

2 ZK496 HOcva BAI5 3 \_____

NH

2 ZK494 'El NBA154N Ose BA90 BA110 OEt ZK341 -H OMe BAI 15N F OEt ZK343 OMe BA159 NNH OEt ZK361 BAI19 -Me H ORt ZK359 e BA1 07 C::Me NH ZK362 N BA124 MeO BA64 BA161 OMe BA65 OMe BA162 84 WO 2007/114926 PCT/US2007/008395 Cpd R1 R2 Cpd RI R2 OH OMe OEt ZK305 O BA24dd H H OMe NH ZK306 ZOH __________ BA43 I N OMe BA66 _ OMe BA91 BA48 BA92 NH O1 O ZK133 -H OH BA86

NH

2 N BA20dd OH BA88 NH2 O BA20d BA96 BA20 BA97 BA99 BA44 H

NH

2 N O BA81dd OH BA156 NH BA81d BA95 , 85 WO 2007/114926 PCT/US2007/008395 Cpd RI R2 Cpd RI R2 -Me O ZK137 -H ZK129 X=CH NI-2 ZK135 -H BA54 / -Me ZK130 -H ZK152 X=CH H 0 ZK128 -H BA42 BA26 86 WO 2007/114926 PCT/US2007/008395 Table 2 Cpd 110a 110p 1105 110y DPK Cpd 110a 110p 1105 loy DPK KS167 ++ + ++ ++ ++ BA46 ++ ++ _+++ ++ +++ ZK141 ++ ++ ++ ++ +++ BA45 ++ + ++ ++ ++ KS84 ++ + ++ + +++ BA39 ++ +++ ++ ++ ZK127 ++ ++ ++ ++ +++ BA150 ++ + ++ ++ ++ ZK134 ++ + ++ ++ ++ BA151 ++ + ++ ++ ++ ZKI132 ++ ++ ++ ++ ++ BA21 ++ ++ ++ ++ ZK125 ++ + ++ ++ +++ BA52 ++ ++ ++ ++ ++ BA56 +++ +++ + +++ +++ BA53 ++ + + + ++ ZK138 ++ ++ ++ ++ +++ BA31 ++ ++ +++ +++ ++ KS287 ++ ++ ++ ++ ++ BA152 ++ ++ ++ ++ +++ KS288 + + + +++ BA149 ++ ++ ++ ++ + KS284 +++ ++ +++ ++ + BA32 ++ ++ +++ ++ BA60 ++ ++ +++ ++ ++ BA55 ++ ++ +++ ++ ++ ZK318 ++ + ++ ++ ++ BA35 ++ +++ +++ +++ ZK320 ++ ++ ++ +++ ++ BA34 ++ ++ +++ ++ +++ ZK333 +++ ++ ++ +++ ++ BA38 ++ .+ ++ . +++ ZK323 +++ ++ + .. .+ + BA40 ++ +4 4 +++ ZK327 +++ ++ +++ +++ ++ BA41 ++ ++ +++ +++ ++ BA77d ++ ++ ++ ++ ++ BA14 ++ ++ +++ ++ +++ BA78d ++ ++ + ++ +++ BA12 ++ ++ + ++ ++ BA22 ++ + +++ +++ ++ BA30 ++ ++ +++ +++ + BA79d +++ +++ +++ +++ +++ ZK149 + ++ ++ ++ + BA85 ++ ++ 4+ ++ ++ ZK126 ++ + ++ + ++ BA87 +++ +++ +++ + ++ ZK143 + + + + + ZK502 ++ ++ ++ I++ +++ ZK150 ++ + + + ++ ZK489 +++ +++ + + ++ ZK136 ++ + + ++ +++ ZK487 +++ +++ +++ +++ ++ ZK131 + + + + + Zk491 +++ ++ + +++ ++ ZK151 + + + + +++ Zk493 +++ +-i- +++ +++ +++ ZK142 + + + + + BA62d .++ +++. ++ + ++ ZK139 + + + ++ ++ ZK450 ++ ++ + +++_ + KS207 ++ + +++ +++ +++ ZK454 ++ ++ ++ +++ +++ KS208 ++ ++ ++ +++ +++ ZK469 +++ +++ ++ .+ + ZK102 + + + + +++ ZK471 +++ +++. +++ +++ ++ ZK1 57 +++ +++ ZK461 +++ ++ +++ ++ ++ ZK159 ++ ++ ++ ++ ++ ZK413 ++ +++ +++ +++ +++ ZK156 ++ ++ ++ ++ +++ ZK379 ++ ++ +++ + ++ KS63 + + + + ++ ZK421 +++ ++ +++ ++ +++ ZK158 ++ ++ ++ ++ +++ ZK403 ++ +++ +++ + ++ ZK147 + ++ ++ ++ ++ ZK405 ++ ++ +++ ++ +++ ZK155 ++ ++ ++ ++ +++ ZK432 ++ ++ +++ +++ +++ ZK162 ++ + ++ ++ +++ ZK434 +++ +++. +++ +++ + ZK165 ++ + ++ ++ +++ ZK465 ++ + +++ +++ + ZK161 ++ + ++ ++ ++ ZK377 ++ ++ ++ +4 +++ ZK167 ++ ++ ZK399 ++ ++ +++ ++ +++ ZK168 ++ +++ ZK401 ++ + ++ + +++ BA116 + ++ ++ ++ +++ BA62 +++ ++ +++ .+ ++ BA17 +++ ++ +++ ++ +++ ZK358 +++ ++ +++ +++ + BA134 ++ + ++ + ++ ZK452 ++ ++ ++ 4++ ++ BA105 ++ ++ +++ ++ +++ ZK456 +++ ++ ++ + + BA122 ++ ++ +++ ++ +++ ZK463 +++ ++ .+ +++ +++ BA11 I +.. .+ +++ +++ +++ ZK371 +++ + +++ +++ ++ BA102 ++ + + +++ +++ ZK409 +++ +++ +++ +++ +++ BAI12 +++ ++ +++ ++ +++ ZK428 +++ ++ +++ +++ ++ BA118 +++ ++ +++, +++ +++ 87 WO 2007/114926 PCT/US2007/008395 Cpd 110a 110p 1108 110y DPK Cpd 110a 1100 1108 110y DPK ZK430 +++ +++ +++ +++ ++ BAI30 +++ ++ +++ +++ +++ ZK387 ++ ++ ++ ++ +++ BA132 +++ +++ +++ +++ +++ ZK389 ++ . +++ +++ ++ +++ BA139 ++ ++ +++ + ++ ZK369 ++ + ++ ++ ++ BA158 +++ ++. ++ +++ ++ ZK385 ++ ++ +++ ++ ++ BA140 + ++ + + ++ ZK391 ++ ++ +++ -++ . +++ BA141 + + + + + BAI 55 2 ++.+ +++ +++ . ++ + BA1 46 + ++.+ + +4+ + BA157 2 +++ ++ +++ -+++ ++ BA142 +++ ++ ++ +++ . + BA59 ++ ++ +++ +++ +++ BA145 ++ ++ ++ ++ ++ BA63 ++ +++ ++ BA147 ++ ++ ++ ++ ++ BA93 +++ + + +++ +. BA148 ++ ++ ++ ++ +++ BA49 ++ + ++ ++ ++ BA143 ++ ++ ++ ++ +++.. BAI5 +++ ++ +++ ++ + +. + BA144 +++ ++ +++ +++ ++ ZK321 +++ ++ + +++ +++ BA129 ++ + ++ + ++ ZK337 +++ +++ +++ +++ +++ BA131 +++ ++ +++ . + +++ ZK347 + +++ +++ +++ +++ BA133 ++ + + +++ + ZK325 +++ +++ +++ +++ ++ BA120 +++ ++ +++ +++ +++. ZK349 +++ I+ +++ +++ +++ BA108 +++ ++ +++ ++ +++ ZK423 +++ ++ +++ +++ + BA121 +++ ++ +++ ++ +++ ZK411 ++ +. + +++ .. BA89 +++ ++ +++ +++ +++ ZK407 ++ +4+ +++ ++ ++ BA94 +++ ++ + +++ +. BA98 + +++ +++ + +++ BA135 + +++ +++ +++. +++ SI ++ + ++ + + BA136 +++ ++ +++ ++ +++ BA23 +++ +++ +++ +++ + BA137 + +++ +++ + ++ ZK485 + +++ ++ ++ ++ BA138 +++ ++ +++ ++. ++ ZK495 +++ ++ +++ ++ +. BA160 ++ ++ ++.+ +++ 44 ZK496 ++ ++ +++ ++ +++i BA157 3 +++ ++ +++ + ++ ZK494 ++ +++ +++ +++. ++ BA154 +++ +++ +++ +++ +++ BA90 +++ +++ +++ +++ ++ BA110 +++ ++ +++ +++ ++ ZK341 ++ ++. + +++ ++ BAI15 +++ ++ +++ .+ ++ ZK343 +++ ++ +++ ++ ++ BA159 +++ ++ +++ + ++ ZK361 ++ ++ +++ +++ ++ - BA119 ++ ++ ++ ++ +++ ZK359 +++ +++ + +++ + BA107 ++ ++ +++ ++ +++ ZK362 + +++ +++ +++ ++ BA124 ++ ++ +++ ++ +++ BA64 + + ++ + ++ BA161 + + + + +++ BA65 + + ++ + ++ BA162 ++ ++ ++ ++ +++ ZK305 + +++ +++ +++ ++ BA24dd ++ ++ +++ ++ +++ ZK306 ++ + ++ ++ ++ BA43 +++ +++ + ++ BA66 ++ ++ +++ ++ +++ BA91 ++ ++ ++ ++ +++ BA48 ++ ++ +++ ++ +++ BA92 ++ ++ +++ ++ +++ ZK133 + + + ++ ++ BA86 ++ ++ ++ ++ ++ BA20dd ++ ++ ++ ++ +++ BA88 + + + +++. +++ BA20d ++ ++ +++ +++ . + BA96 ++ + +++ ++ +++ BA20 ++ ++ ++ ++ BA97 4+ + +++ +++ + BA99 ++ + ++ + ++ BA44 ++ +++ ++ ++ ++ BA81dd +++ ++ +++ +++ + BA156 ++ ++ ++ ++ +++ BA81d +++ ++ +++ +++ ++ BA95 ++ ++ +++ +++ .+++ ZK137 ++ + ++ ++ +++ ZK129 ++ ++ ++ ++ +++ ZK135 ++ + + ++ ++ BA54 ++ ++ ++ ++ +++ ZK130 + + + + + ZK152 ++ ++ ++ ++ +++ ZK128 ++ + ++ ++ ++ BA42 ++ ++ ++ ++ +++ BA26 ++ ++ +++ +++ ++ P1K294 ++ +. +++ ++ ++ SU11248 ++ + ++ ++ + fressa + + + + + BAY43- + 9006 ++ + + + PIK103 +++ +++ +++ +++ + Dasatinib ++ + ++ + ++ PIK90 ++ ++ +++ +++ +++ 88 WO 2007/114926 PCT/US2007/008395 Table 3 Cpd Abi Hck Src Src (T/1) VEGFR EGFR EphB4 KS84 + +++ ++ ++ +++ + +++ BA56 ++ +++ ++ ++ ++ +++ ++ KS284 +++ +++ ++ ++ +++ +++ +++ BA60 ++ +++ + +++ ++ + ++ ZK318 ++ ++ +++I ++ + ++ ZK320 +++ +++ ++ ++ ++ ++ ++ ZK333 + +++ ++ ++ + ++ ++ ZK323 +++ + +++ +++ +++ +++ +++ ZK327 +++ +++ +++ ++ ++ ++ ++ BA77d +++ .+ +++ ++ ++ ++ ++ BA78d +++ +++ +++ ++ ++ ++ ++ BA22 +++ +++ + + ++ +++ +++ +++ BA79d +++ +++ +++ ++ +++ + +++ BA85 ++ +++ +++ ++ ++ ++ ++ BA87 ++.++ + + +++ + +++ +++ ZK502 +++ +++ + ++ ++ ++ + ZK489 +++ +++ +++ + ++ + ++ ZK487 +++ +++ +++ ++ +++ +++ +++ Zk491 +++ +++ + ++ +++ + ++ Zk493 +++ +++ +++ ++ +++ + ++ BA62d +++ +++ ++ +4 +44 ++ + ZK450 + +++ + + ++ + ++ ZK454 +++ ++ +++ + ++ ++ + ZK469 +++ +++ +++ + ++ ++ ++ ZK471 +++ +++ +++ + ++ ++ + ZK461 +++ +++ +++ + ++ ++ ++ ZK413 +++ +++ +++ + ++ ++ ZK379 + +++ +++ ++ + +++ ++ ZK421 +++ +++ +++ +++ +++ ++ ++ ZK403 +++ +++ +++ ++ +++ ++ +++ ZK405 +++ +++ +++ ++ ++ ++ + ZK432 +++ ++ +++ ++ +++ +++ ZK434 +++ +++ ++ ++ +++ ++ +++ ZK465 +++ +++ + + +++ +++ +++ ZK377 ++ ++ ++ + ++ + + ZK399 +++ +++ ++ + + + ++ ZK401 +++ +++ +++ + + + + BA62 + +++ ++ + + ++ +++ ZK358 + +++ +++ ++ + ++ ZK452 +++ +++ +++ ++ +++ ++ ++ ZK456 +++ +++ +++ + ++ ++ ++ ZK463 +++ +++ +++ ++ + ++ ++ ZK371 +++ +++ +++ ++ +++ +++ +++ ZK409 + +++ +++ ++ ++ ++ +++ ZK428 +++ +++ +++ ++ +++ ++ + ZK430 +++ + +++ ++ ++ ++ +++ ZK387 +++ +++ +++ + ++ ++ ++ ZK389 +++ +++ +++ ++ +++ ++ ++ ZK369 ++ ++ +++ + ++ ++ + ZK385 ++ +++ +++ + ++ + ++ ZK391 ++ +++ +++ + ++ ++ ++ BA155 2 ++ +++ +++ ++ ++ + + BA157 2 ++ ++ ++ ++ ++ ++ ++ 89 WO 2007/114926 PCT/US2007/008395 Cpd Abi Hck Sre Src (TilI) VEGFR EGFR EphB4 BA59 +++ +++ +++ +++ ++ ++ ++ BA63 ++ +++ ++ ++ ++ ++ ++ BA93 ++ +++ +++ ++ ++ ++ ++ BA49 ++ +++ +++ ++ + ++ + + BA15 ++ +++ +++ ++ + +++ ++ ZK321 +++ +++ +++ ++ ++ + ++ ZK337 +++ +++ +++ + ++ ZK347 +++ + + ++ +++ .+ ++ ZK325 +++ +++ ++ ++ +++ ++ +++ ZK349 +++ +++ +++ +++ +++ +++ +++ ZK423 +++ +++. +++ ++ +++ ++. +. 4 ZK411 ++ ++ +++ + ++ ++ ++ ZK407 ++ +++ +++ + +++ ++ + BA98 +++ +++ ++ ++ + +++ ++ Si. +++ + ++ + + + + BA23 ++ ++ ++ ++ + ++ ++ ZK485 ++ +++ +++ + + ++ ++ ZK495 ++ +++ + ++ + ++ ++ ZK496 ++ ++ ++ ++ ++ ++ ++ ZK494 +++ +++ +++ ++ ++ ++ ++ BA90 ++ +++ ++..+ ++ ++ ++ ++ ZK341 ++ ++ + + + + + ZK343 ++ +++ ++ + ++ ++ ++ ZK361 ++ ++ ++ + + ++ + ZK359 +++ + +++ ++ ++ ++ +++ ZK362 ++ +++ +++ + + ++ + BA64 +++ +++ + ++ + ++ ++ BA65 + + +++ ++ ++ ++ ++ ZK305 ++ ++ ++- ++ + + ++ ZK306 + ++ ++ ++ ++ ++ + BA66 ++ ++ + + + ++ BA48 ++ +++ +4 ++ ++ ++ ++ BA20dd +++ +.++ + ++ ++ ++ ++ BA20d +++ +++ +++ ++ ++ ++ ++ BA20 +++ +++ + +++ ++ +++ + BA99 ++ + +++ ++ + ++ ++ BA81dd .+ +++ ++ ++ +++ +++ +++ BA81d + +++ + ++ +++ +++ +++ BA26 ++ ++ +++ ++ + + + BA46 ++ ++ ++ + ++ ++ ++ BA45 ++ +++ +++ ++ ++ ++ + BA39 ++ ++ ++ ++ ++ + ++ BA150 ++ ++ ++ + ++ + ++ BA151 ++ ++ ++ + + ++ ++ BA21 ++ ++ ++ + + + + BA52 ++ ++ ++ + + + + BA53 ++ ++ ++ + + + + BA31 ++ ++ ++ + + ++ + BA152 +++ +++ ++ + ++ ++ ++ BA149 ++ + + ++ ++ ++ ++ BA32 ++ ++ ++ + + + ++ BA55 ++ ++ ++ + + ++ ++ BA35 ++ ++ ++ ++ ++ ++ ++ BA34 ++ ++ +4 ++ ++ ++ ++ BA38 ++ 4+ ++ ++ + + + BA40 ++ ++ ++ ++ ++ ++ + 90 WO 2007/114926 PCT/US2007/008395 Cpd Abi Hok Src Src (TII) VEGFR EGFR EphB4 BA41 ++ ++ ++ ++ ++ + ++ OA14 ++ ++ ++ ++ + + ++ BA12 ++ ++ ++ ++ ++ ++ ++ BA30 ++ ++ ++ ++ ++ +++ ++ KS208 ++ +++ ++ ++ ++ +++ ++ BAI16 ++. +++ ++ +++ ++ ++ BA17 +++ +++ +++ +++ +++ ++ ++ BA134 ++ ++ ++ ++ + + ++ BA105 ++ +++ ++ ++ ++ ++ ++ BA122 +++ +++ +++ ++ ++ +++ +++ BAII + + ++ ++ ++ ++ ++ BA102 +++ +++ ++ ++ +++ +++ +++ BAI12 ++ +++ +++ ++ ++ ++ ++ BA118 ++ ++ + ++ ++ + ++ BA130 ++ +++ ++ ++ +++ + ++ BA132 ++ +++ ++ + ++ ++ ++ BA139 ++ ++ ++ + ++ ++ + BA158 +++ +++ +++ ++ ++ ++ ++ BA140 ++ ++ ++ ++ + ++ ++ BA141 + ++ + + + ++ + BA146 ++ ++ ++ + ++ ++ ++ BA142 ++ ++ +++ + ++ ++ ++ BA145 + ++ ++ + + + ++ BA147 ++ ++ ++ + ++ + ++ BA148 + ++ ++ + + ++ + BA143 ++ ++ ++ ++ + ++ ++ BA144 ++ ++. ++ + ++ + ++ BA129 ++ + +++ + ++ ++- ++ BA131 ++ ++ 11 + ++ + ++ BA133 ++ ++ +++ + + ++ ++ BA120 +++ +++ +++ .+++ ++ ++ BA108 +++ +++ ++. +. ++ +++ +++ BA121 +++. +++ . +++ ++. +++ +++ . BA89 +++ +++. +++ +++4 +++ ++ +++ BA94 +++ +++. ++ +++ +++ .+ ++ BA135 +++ +++. ++ ++ +++ +++ + BA136 +++ + + ++ ++ BA137 +++ +++. ++ +++ +++ ++- ++ BA138 +++ +++ +++ +++ +++ +++ ++ BA160 ++ ++ +++ . ++ ++ +++ ++ BA157 3 ++ +++ +++ ++ + ++ ++ BA154 +.++ ++. + ++ ++ ++ ++ BA110 + +++ . ++ ++ ++ ++ BAI15 +++- +++ +++. . +++ +++ ++ BA159 +++ +++ +++ ++ +++ ++ ++ BAi9 ++ +++ +++ ++ ++ ++ ++ BA107 +++ +++ +++ + +++ +++ +++ BA124 +++ +++ +++ ++ ++ ++ ++ BA161 ++ + ++ + + ++ + BA162 ++ ++ ++ + + ++ ++ BA24dd ++ ++ ++ ++ ++ ++ ++ BA43 ++ +++ + + ++ ++ ++ BA91 ++ +++ . ++ ++ I ++ -++ BA92 ++ +++ +++ ++ ++ ++ ++ BA86 +++ ++.+ +++. +++. +++ + BAB8 ,.+++ +++. +-- ++ ++ +++ , +++ 91 WO 2007/114926 PCT/US2007/008395 Cpd Abi Hck Src Src (TI) VEGFR EGFR EphB4 BA96 +++ +++ ++ ++ ++ +++ +++ BA97 +++ +++ + ++ ++ ++ BA44 ++ ++ ++ ++ + ++ + BA156 ++ ++ ++ ++ ++ +++ ++ BA95 ++ I-+++ ++ + + ++ ++ BA54 ++ ++ +++ ++ ++ ++ ++ BA42 + ++ ++ ++ ++ + ++ SU11248 +++ +4 +++ +++ + ++ + BAY43 9006 +.+ . +++ +++ +++ +++ + ++ Dasatinib ++ + ++ Iressa ++ ++ ++ ++ ++ ++ PIK103 + + + + + + + PIK90 + + + + + + + PIK294 ++ + ++ + + + + Table 4 Cpd cKIT Tie2 FLT3 PDGFR RET IR mTOR ZK358 +++ ++ +++ +++ ++ ++ +++ ZK487 +++ +++ ++ +++ ++ + + ZK349 +++ +++ +++ ++ +++ ++ +.+ ZK494 +++ ++ ++ +++ ++ + ++ BA102 +++ +++ +++ + +++ + ++ BA121 +++ ... .+ +++ ++ ++ KS84 +++ + +++ +++ +++ ++ ++ SU11248 +++ ++ +++ +++ +++ ++ + BAY43-9006 +++ +++ + +++ + ++ + Dasatinib +++ ++ +++ +++ ++ + + Iressa + ++ +++I ++ ++ + + In Tables 2-4 above, a +++ indicates an IC50 of less than 1 pM; a ++ indicates an IC50 of from 1 pM to 50 pM; and a + indicates and IC50 of more than 50 kM. 92 WO 2007/114926 PCT/US2007/008395 IX. 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Claims (46)

1. A compound having the formula: R 36 R

2 N -N X R(1) wherein X is =N- or =C(H)-; 5 R' is hydrogen, R-substituted or unsubstituted alkyl, R 3 -substituted or 5 unsubstituted heteroalkyl, R 3 -substituted or unsubstituted cycloalkyl, R 3 -substituted or 7 unsubstituted heterocycloalkyl, R?-substituted or unsubstituted aryl, or R-substituted or 8 unsubstituted heteroaryl; 9 R 2 is halogen, R 4 -substituted aryl, or substituted or unsubstituted heteroaryl; O R 3 is halogen, -CN, -OR 5 , -S(O),R 6 , -NR 7 R, -C(O)R!, =N-NH 2 , -NR'O 1 C(O)R", -NR1 2 -C(O)-OR1 3 , -C(O)NR1 4 R 5 , -NR1 6 S(O)2R' 7 , -S(O) 2 NR1 8 , R1 9 -substituted or 2 unsubstituted alkyl, R 19 -substituted or unsubstituted heteroalkyl, R 19 -substituted or 3 unsubstituted cycloalkyl, R1 9 -substituted or unsubstituted heterocycloalkyl, R1 9 -substituted or 4 unsubstituted aryl, or R 9 -substituted or unsubstituted heteroaryl, wherein n is an integer from 5 Oto2; 6 R 3 6 is -NR 3 7 R 38 or halogen; 7 R 4 is halogen, -CN, -OR 2 0 , -S(O)qR 2 1 , -R 2 R 3 , -C(O)R 2 4 , =NNH 2 , N25_ l8 C(O)R 2 6 , _N 2 7 -C(O)-OR 2 8 , -C(O)NRe 9 R 30 , -NRS(O) 2 R 2 , -S(O) 2 NR, R 3 4 -substituted or .9 unsubstituted alkyl, R 34 -substituted or unsubstituted heteroalkyl, R 3 4 -substituted or 2O unsubstituted cycloalkyl, R 34 -substituted or unsubstituted heterocycloalkyl, R 34 -substituted or Z1 unsubstituted aryl, or R 34 -substituted or unsubstituted heteroaryl, wherein q is an integer from Z2 0 to 2; 23 R 5 , R 6 , R 7 , R 8 , R!, R' 0 , R1, R 2 , R 13 , R1 4 , R1 5 , R1 6 , R1 7 , R1 8 , R 20 , R 21 , R 2 , R

3 , Z4 R 24 , R, R 2 6 , R 7 , R 2 8 , R 2 9 , R 30 , R, R 32 , and R? 3 are independently hydrogen, R 3 s-substituted Z5 or unsubstituted alkyl, R- 35 substituted or unsubstituted heteroalkyl, unsubstituted cycloalkyl, Z6 R 35 -substituted or unsubstituted heterocycloalkyl, R 35 -substituted or unsubstituted aryl, or Z7 R 3 5 -substituted or unsubstituted heteroaryl; 98 WO 2007/114926 PCT/US2007/008395 8 R 9 , R 34 and R1 5 are independently hydrogen, halogen, unsubstituted alkyl, 9 unsubstituted heteroalkyl, unsubstituted cycloalkyl, unsubstituted heterocycloalkyl, 0 unsubstituted aryl, or unsubstituted heteroaryl; and 1 R 3 7 and R 38 are hydrogen, halogen, or unsubstituted alkyl. 1 2. The compound of claim 1, wherein R 2 is \W1 4 2 W 2 - W 3 3 wherein 4 W', W 2 , W 3 , and W 4 are independently =CH-, =CR 4 -, or =N-; and 5 ring A is a partially or fully unsaturated 6- or 7- membered ring. L 3. The compound of claim 1, wherein R 5 , R 6 , R 7 , R, R?, R 0 , R 1 1, R 1, 2 R 1, R14, R 1, R 16 , R 17 , R 8 , R 20 , R 2 1 , R 2 , R 3 , R 2 4 , R 2 5 , R 6 , R 7 , R 2 8 , R 2 9 , R 30 , RI, R? 2 , and 3 R 3 are independently hydrogen, unsubstituted alkyl, unsubstituted heteroalkyl, unsubstituted I cycloalkyl, unsubstituted heterocycloalkyl, unsubstituted aryl, or unsubstituted heteroaryl.

4. The compound of claim 1, wherein R 2 0 , R 21 , R 2 , R 3 , R 2 4 , R 5 , R 6 , R 2 7 , R, R29, R, R , R 2 , and R? 3 are independently hydrogen, unsubstituted alkyl, or unsubstituted heteroalkyl.

5. The compound of claim 1, wherein R' is R-substituted or 2 unsubstituted alkyl, R 3 -substituted or unsubstituted cycloalkyl, or R 3 -substituted or 3 unsubstituted aryl. 1

6. The compound of claim 1, wherein R 1 is R?-substituted or 2 unsubstituted alkyl, or R-substituted or unsubstituted cycloalkyl. 1

7. The compound of claim 1, wherein R 1 is R 3 -substituted or 2 unsubstituted C 1 -C 4 alkyl, or R 3 -substituted or unsubstituted C 3 -C 6 cycloalkyl. 1

8. The compound of claim 1, wherein R 1 is R 3 -substituted or 2 unsubstituted Ci-C 4 alkyl, or R?-substituted or unsubstituted cyclopentyl. 99 WO 2007/114926 PCT/US2007/008395 1

9. The compound of claim 1, wherein R' is methyl or unsubstituted C 3 -C 6 2 branched alkyl. 1

10. The compound of claim 1, wherein R 1 is isopropyl. 1

11. The compound of claim 1, wherein R 3 is R' 9 -substituted or 2 unsubstituted alkyl, R 19 -substituted or unsubstituted cycloalkyl, or R 19 -substituted or 3 unsubstituted aryl. 1

12. The compound of claim 1, wherein R 3 is R 19 -substituted or 2 unsubstituted alkyl, R 19 -substituted or unsubstituted cycloalkyl, or R 19 -substituted or 3 unsubstituted aryl. 1

13. The compound of claim 1, wherein R 3 is R1 9 -substituted or 2 unsubstituted alkyl, or R 19 -substituted or unsubstituted cycloalkyl. 1

14. The compound of claim 1, wherein R1 9 is unsubstituted alkyl or 2 unsubstituted cycloalkyl. 1

15. The compound of claim 1, wherein R 19 is unsubstituted C 1 -C 4 alkyl or Z unsubstituted cyclopentyl.

16. The compound of claim 1, wherein R 2 is R 4 -substituted aryl, or R4 substituted or unsubstituted heteroaryl. 1

17. The compound of claim 1, wherein R 2 is R 4 -substituted phenyl, R 4 2 substituted or unsubstituted naphthyl, R 4 -substituted or unsubstituted pyridinyl, R 4 3 substituted or unsubstituted pyrimidinyl, R 4 -substituted or unsubstituted thiophenyl, R 4 4 substituted or unsubstituted furanyl, R 4 -substituted or unsubstituted indolyl, R 4 -substituted or 5 unsubstituted benzoxadiazolyl, R 4 -substituted or unsubstituted benzodioxolyl, R-substituted 6 or unsubstituted benzodioxanyl, R 4 -substituted or unsubstituted thianaphthanyl, R 4 7 substituted or unsubstituted pyrrolopyridinyl, R 4 -substituted or unsubstituted indazolyl, R 4 8 substituted or unsubstituted tetrahydronaphthalenyl, R 4 -substituted or unsubstituted 9 quinolinyl, R 4 -substituted or unsubstituted quinoxalinyl, R 4 -substituted or unsubstituted 0 pyridopyrazinyl, R 4 -substituted or unsubstituted quinazolinonyl, R 4 -substituted or I unsubstituted chromenonyl, R 4 -substituted or unsubstituted benzoisoxazolyl, R 4 -substituted 100 WO 2007/114926 PCT/US2007/008395 2 or unsubstituted imidazopyridinyl, R 4 -substituted or unsubstituted benzofuranyl, R 4 3 substituted or unsubstituted dihydro-benzofuranyl, R 4 -substituted or unsubstituted dihydro 4 benzodioxinyl, R 4 -substituted or unsubstituted benzoimidazolonyl, or R 4 -substituted or 5 unsubstituted benzothiophenyl. 1

18. The compound of claim 1, wherein R 2 is R 4 -substituted phenyl, R 4 2 substituted or unsubstituted pyrrolpyridinyl, R 4 -substituted or unsubstituted quinolinyl, R 4 3 substituted or unsubstituted indazolyl, R 4 -substituted or unsubstituted quinolinyl indolyl, or 4 R 4 -substituted or unsubstituted naphthyl. 1

19. The compound of claim 18, wherein R 4 is halogen, -CN, -OR20, or 2 -NR 22 R 23 . 1

20. The compound of claim 18, wherein R 4 is halogen, or -OR 2 0 . 1

21. The compound of claim 20, wherein R 2 0 is hydrogen or unsubstituted 2 Ci-Cio alkyl. 1

22. The compound of claim 20, wherein R 20 is hydrogen or unsubstituted 2 Ci-C 4 alkyl. 1

23. The compound of claim 20, wherein R 2 0 is hydrogen or methyl. 1

24. The compound of claim 1, wherein R 2 has the formula: OH OH R4 ,or OH 2 , wherein 3 R4 is absent, halogen, unsubstituted C 1 -C 4 alkyl, or -OR 2 0 , wherein R20 is 4 unsubstituted CI-C 4 alkyl. 1

25. The compound of claim 1, wherein R 2 is 6-hydroxynaphthyl, 2 unsubstituted 7-azaindole, unsubstituted indolyl, unsubstituted indazolyl, or unsubstituted 3 quinolinyl. 1

26. The compound of claim 1, wherein X is =N-. 101 WO 2007/114926 PCT/US2007/008395

27. The compound of claim 1, wherein R 6 is -NH 2 .

28. A pharmaceutical composition comprising the compound of claim 1 2 and a pharmaceutically acceptable excipient. 1

29. A method of decreasing the catalytic activity of a P13 kinase, the 2 method comprising the step of contacting said P13 kinase with an activity decreasing amount 3 of an antagonist, wherein said antagonist is a P13-Kinase affinity pocket binding antagonist. 1

30. The method of claim 29, wherein said antagonist is a PI3-Kinase 2 affinity pocket binding pyrazolopyrimidine antagonist or a P13-Kinase affinity pocket binding 3 pyrrolopyrimidine antagonist. 1

31. The method of claim 29, wherein said antagonist is capable of 2 decreasing the catalytic activity of a tyrosine kinase. 1

32. The method of claim 29, wherein said antagonist is capable of 2 decreasing the catalytic activity of a mTOR. 1

33. The method of claim 29, wherein said antagonist is capable of 2 decreasing the catalytic activity of a mTOR and a tyrosine kinase. 1

34. The method of claim 29, wherein said P13 kinase is p11 Oa. 1

35. A method of decreasing the catalytic activity of a P13 kinase, the 2 method comprising the step of contacting said P13 kinase with an activity decreasing amount 3 of an antagonist, wherein said antagonist the formula: R

36 R 2 N N 4 RI (I) 5 wherein 6 X is =N- or =C(H)-; 7 R' is hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted 8 heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted 102 WO 2007/114926 PCT/US2007/008395 9 heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; 0 and 1 R 2 is halogen, substituted or unsubstituted alkyl, substituted or unsubstituted 2 heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted 3 heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; 4 R 3 is halogen, -NR 7 R 38 , substituted or unsubstituted alkyl, substituted or 5 unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted 6 heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; 7 and 8 R 37 and R 38 are independently hydrogen, substituted or unsubstituted alkyl, 9 substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or D unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or 1 unsubstituted heteroaryl. 1 36. The method of claim 35, wherein: 2 -R is hydrogen, R 3 -substituted or unsubstituted alkyl, R-substituted or 3 unsubstituted heteroalkyl, R 3 -substituted or unsubstituted cycloalkyl, R 3 -substituted or I unsubstituted heterocycloalkyl, R-substituted or unsubstituted aryl, or R3-substituted or 5 unsubstituted heteroaryl; 5 R 2 is halogen, R 4 -substituted aryl, or substituted or unsubstituted heteroaryl; 7 R 3 is halogen, -CN, -OR:, -S(O),R 6 , -NRR, -C(O)R?, =N-NH 2 , -NRWO 3 C(O)R", -NR' 2 -C(O)-OR 3 , -C(O)NR1 4 R 5 , -NR16 S(O) 2 R' 1, -S(O) 2 NR'B, R1 9 -substituted or 9 unsubstituted alkyl, R 9 -substituted or unsubstituted heteroalkyl, R1 9 -substituted or 0 unsubstituted cycloalkyl, R 9 -substituted or unsubstituted heterocycloalkyl, R' 9 -substituted or 1 unsubstituted aryl, or R' 9 -substituted or unsubstituted heteroaryl, wherein n is an integer from 2 0 to 2; 3 R 36 is NR

3 7 R 38 or halogen; 4 R 4 is halogen, -CN, -OR 20 , -S(O)qR, -NR 22 R 3 , -C(O)R 24 , =N-NH 2 , -NR 5 C(O)R 2 6 , NR 2 7 -C(O)-OR 2 8 , -C(O)NR 2 9 R 3 0 , -NRS(O) 2 R 2 , -S(O) 2 NR 3 , R 34 -substituted or 6 unsubstituted alkyl, R 34 -substituted or unsubstituted heteroalkyl, R 34 -substituted or 7 unsubstituted cycloalkyl, R 34 -substituted or unsubstituted heterocycloalkyl, R 34 -substituted or 8 unsubstituted aryl, or R 34 -substituted or unsubstituted heteroaryl, wherein q is an integer from 9 0 to 2; 103 WO 2007/114926 PCT/US2007/008395 0 R, R 6 , R 7 , R, R?, R1 0 , R' ", R, 12 R"1, R 1 4 , R1 5 , R 1, R, 1 7 R 18 ', R 20 , R 2 , R, R 23 , 1 R 2 4 , R 2 , R 26 , R 2 7 , R 2 8 , R 2 9 , R 0 , R? 1 , R 3 2 , and R 33 are independently hydrogen, R 5 -substituted 2 or unsubstituted alkyl, R 5 -substituted or unsubstituted heteroalkyl, unsubstituted cycloalkyl, 3 R 35 -substituted or unsubstituted heterocycloalkyl, R 5 -substituted or unsubstituted aryl, or 4 ,R 3 5 -substituted or unsubstituted heteroaryl; 5 R 1 9 , R 3 4 and R1 5 are independently hydrogen, halogen, unsubstituted alkyl, 6 unsubstituted heteroalkyl, unsubstituted cycloalkyl, unsubstituted heterocycloalkyl, 7 unsubstituted aryl, or unsubstituted heteroaryl; and 8 R 7 and R 38 are hydrogen, halogen, or unsubstituted alkyl. 1 37. The method of claim 35, wherein R 3 6 is -NH 2 . 1

38. The method of claim 35, wherein R 2 has the formula: W1 4 2 W 2 -W 3 (II 3 wherein I W1, W 2 , W 3 , and W 4 are independently =CH-, =CR 4 -, or =N-; and 5 ring A is a partially or fully unsaturated 6- or 7- membered ring.

39. A method of treating a disease mediated by P13 kinase activity, or P13 Kinase activity and Tyrosine Kinase Activity, in a subject in need of such treatment, said 3 method comprising administering to said subject a therapeutically effective amount of an 4 antagonist, wherein said antagonist is a P13-Kinase affinity pocket binding 5 pyrazolopyrimidine antagonist or a P13-Kinase affinity pocket binding pyrrolopyrimidine 6 antagonist. 1

40. The method of claim 39, wherein said disease is liver cancer, colon 2 cancer, breast cancer, melanoma, acute myelogenous leukemia, chronic myelogenous 3 leukemia, or nonsmall-cell lung cancer. 1

41. A method of treating a disease mediated by PI3 kinase activity, or P13 2 Kinase activity and Tyrosine Kinase Activity, in a subject in need of such treatment, said 104 WO 2007/114926 PCT/US2007/008395 3 method comprising administering to said subject a therapeutically effective amount of an I antagonist, wherein said antagonist has the formula: R 36 R 2 N ~ x N N 5 RI 5 wherein 7 X is =N- or =C(H)-; 3 R' is hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted ) heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted ) heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; I and 2 R 2 is halogen, substituted or unsubstituted alkyl, substituted or unsubstituted 3 heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted I heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; 5 R1 6 is halogen, -NR 3 7 R 38 , substituted or unsubstituted alkyl, substituted or 5 unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted 7 heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; 3 and R? 7 and R 3 8 are independently hydrogen, substituted or unsubstituted alkyl, ) substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or I unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or 2 unsubstituted heteroaryl. 1

42. The method of claim 41, wherein: 2 R1 is hydrogen, R 3 -substituted or unsubstituted alkyl, R 3 -substituted or 3 unsubstituted heteroalkyl, R 3 -substituted or unsubstituted'cycloalkyl, R 3 -substituted or 4 unsubstituted heterocycloalkyl, R 3 -substituted or unsubstituted aryl, or R3-substituted or 5 unsubstituted heteroaryl; 6 R 2 is halogen, R 4 -substituted aryl, or substituted or unsubstituted heteroaryl; 7 R 3 is halogen, -CN, -OR, -S(O)nR 6 , -NR 7 R", -C(O)R 9 , =N-NH 2 , -NR"1 8 C(O)R", -NR 12 -C(O)-OR 13 , -C(O)NR1 4 Ri 5 , -NR 1 6 S(O) 2 R 17 , -S(O) 2 NR 1 8, R1 9 -substituted or 9 unsubstituted alkyl, R' 9 -substituted or unsubstituted heteroalkyl, R 19 -substituted or 105 WO 2007/114926 PCT/US2007/008395 0 unsubstituted cycloalkyl, R' 9 -substituted or unsubstituted heterocycloalkyl, R 19 -substituted or 1 unsubstituted aryl, or R1 9 -substituted or unsubstituted heteroaryl, wherein n is an integer from 2 0 to 2; 3 R is NR7 R3 or halogen; 4 R 4 is halogen, -CN, -OR 2 0 , -S(O)qR? 1 , -NR 2 R', -C(O)R 24 , =N-NH 2 , -NR 2 s_ 5 C(O)R , -NR-C(O)-ORU' _C(O)NR-0R3, -NR'S(O) 2 R 32 , -S(O) 2 NR 33 , R4-substituted or 5 unsubstituted alkyl, R 34 -substituted or unsubstituted heteroalkyl, R 34 -substituted or 7 unsubstituted cycloalkyl, R 34 -substituted or unsubstituted heterocycloalkyl, R 34 -substituted or B unsubstituted aryl, or R 34 -substituted or unsubstituted heteroaryl, wherein q is an integer from S0 to 2; 3 R 5 , R 6 , R 7 , R, R?, R' 0 , R", R12, R1 3 , R 14 , R1 5 , R 6 , R 17 , R'8, R 2 0 , R , R 2 2 , R 2 , I R 24 , R 25 , R 6 , R 2 , R 2 , R 29 , R 30 , R 3 , R 3 , and RM are independently hydrogen, R 5 -substituted 2 or unsubstituted alkyl, R 35 -substituted or unsubstituted heteroalkyl, unsubstituted cycloalkyl, 3 R 35 -substituted or unsubstituted heterocycloalkyl, R- 35 substituted or unsubstituted aryl, or t R 35 -substituted or unsubstituted heteroaryl; 5 R' 9 , R 34 and R 5 are independently hydrogen, halogen, unsubstituted alkyl, 5 unsubstituted heteroalkyl, unsubstituted cycloalkyl, unsubstituted heterocycloalkyl, 7 unsubstituted aryl, or unsubstituted heteroaryl; and R 7 and R 3 8 are hydrogen, halogen, or unsubstituted alkyl.

43. The method of claim 41, wherein R 36 is -NH 2 . 1

44. The method of claim 41, wherein R 2 has the formula: \W1 (*A 4 2 W 2 W 3 (Ill, 3 wherein 4 W', W 2 , W 3 , and W 4 are independently =CH-, =CR 4 -, or =N-; and 5 ring A is a partially or fully unsaturated 6- or 7- membered ring. 1

45. The method of claim 40, wherein said disease is liver cancer, colon 2 cancer, breast cancer, melanoma, acute myelogenous leukemia, chronic myelogenous 3 leukemia, or nonsmall-cell lung cancer. 106 WO 2007/114926 PCT/US2007/008395 1

46. A method of disrupting the function of a leukocyte or disrupting a 2 function of an osteoclast, said method comprising contacting said leukocyte or said osteoclast 3 with a function disrupting amount of an antagonist, wherein said antagonist is a P13-Kinase 4 affinity pocket binding pyrazolopyrimidine antagonist or a P13-Kinase affinity pocket binding 5 pyrrolopyrimidine antagonist. 107