AU764782B2

AU764782B2 - Substituted indolinones, the production thereof and their use as medicaments

Info

Publication number: AU764782B2
Application number: AU43707/99A
Authority: AU
Inventors: Wolfgang Grell; Armin Heckel; Norbert Redemann; Jacobus C. A. Van Meel; Rainer Walter
Original assignee: Boehringer Ingelheim Pharma GmbH and Co KG; Boehringer Ingelheim Pharmaceuticals Inc
Current assignee: Boehringer Ingelheim Pharma GmbH and Co KG
Priority date: 1998-06-04
Filing date: 1999-05-28
Publication date: 2003-08-28
Anticipated expiration: 2019-05-28
Also published as: NO20006138D0; IL138702A0; HRP20000831A2; ID27035A; JP2002516906A; TR200003515T2; YU73900A; KR20010043973A; EA200100001A1; HUP0102210A2; WO1999062882A1; PL344467A1; AU4370799A; EA003514B1; CA2328291A1; BR9910898A; SK18222000A3; EP1100779A1; EE200000723A; HUP0102210A3

Description

1 S018548aus Boehringer Ingelheim Pharma KG Case 5/1239-FL D-55216 INGELHEIM Foreign filing text New substituted indolinones, the preparation thereof and their use as pharmaceutical compositions The present invention relates to new substituted indolinones of general formula

R

3 I3 R 4 N N

RI

the isomers thereof and the salts thereof, particularly the physiologically acceptable salts thereof which have valuable properties.

The above compounds of general formula I wherein R, denotes a hydrogen atom or a prodrug group have valuable pharmacological properties, particularly an inhibitory effect on various kinases, particularly on complexes of CDKs (CDK1, CDK2, CDK3, CDK4, CDK6, CDK7, CDK8 and CDK9) with their specific cyclines Bl, B2, C, Dl, D2, D3, E, F, Gl, G2, H, I and K) and viral cycline (cf. L. Mengtao in J. Virology 71(3), 1984-1991 (1997)), and the other compounds of the above general formula I wherein R, does not represent a hydrogen atom or a prodrug group, are valuable intermediate products for preparing the abovementioned compounds.

2 The present invention thus relates to the above compounds of general formula I, whilst the compounds wherein R, denotes a hydrogen atom or a prodrug group have valuable pharmacological properties, the pharmaceutical compositions containing the pharmacologically active compounds, their use and processes for preparing them.

In the above general formula I X denotes an oxygen or sulphur atom, R, denotes a hydrogen atom, a C 14 -alkoxy-carbonyl or C2_4-alkanoyl group,

R

2 denotes a carboxy or C 1 4 -alkoxy-carbonyl group or an aminocarbonyl group optionally substituted by one or two

C

13 -alkyl groups, whilst the substituents may be identical or different,

R

3 denotes a hydrogen atom or a C 1 6 -alkyl group which may be substituted at the 2 position, in relation to the carbon atom of the R 3

-C(R

4 NRs)= group by a fluorine, chlorine or bromine atom, by a hydroxy, Cl_ 3 -alkoxy, C, 3 -alkylsulphenyl,

C

1 -3-alkylsulphinyl, C 1 3 -alkylsulphonyl, phenylsulphenyl, phenylsulphinyl, phenylsulphonyl, amino, C,_ 3 -alkylamino, di- (C 1 3 -alkyl)-amino, C 2 5 -alkanoylamino or N-(C_.3-alkylamino) -C2- 5 -alkanoylamino group,

R

4 denotes a hydrogen atom, a C_ 6-alkyl group or a Cs,_-cycloalkyl group optionally substituted by a C 1 3 -alkyl group wherein a methylene group in the 3 or 4 position in relation to the carbon atom of the R 3

-C(R

4

NR

5 group may be substituted by an imino group optionally substituted by a

C._

3 -alkyl group, a phenyl or naphthyl group which may be substituted -3by a fluorine, chlorine, bromine or iodine atom, by a methoxy group optionally substituted by 1 to 3 fluorine atoms, by a C 2 -3-alkoxy which may be substituted in the 2 or 3 position by a Cl 1 3 -alkylamino, di-(C 1 3 -alkyl)-amino or to 7-membered cycloalkyleneimino group, whilst additionally an alkyl moiety in the abovementioned alkylamino and dialkylamino groups may be substituted by a phenyl group, by a trifluoromethyl, amino, C 1 3 -alkylamino, di-

(C

13 -alkyl)-amino, C 2 -5-alkanoylamino, N-(C 13 -alkyl)-

C

2 5 -alkanoylamino, C, -alkylsulphonylamino, N- (C 3 -alkyl) C, alkylsulphonylamino, phenylsulphonylamino,

N-(C-

3 -alkyl)-phenylsulphonylamino, aminosulphonyl,

C,

3 -alkylaminosulphonyl or di-(C, 3 -alkyl)-aminosulphonyl group, whilst additionally an alkyl moiety in the abovementioned alkylamino and dialkylamino groups may be substituted by a phenyl group, by a carbonyl group which is substituted by a hydroxy,

C

1 3 -alkoxy, amino, C 1 3 -alkylamino or N- (C,,-alkyl)-

C

1 3 -alkylamino group, whilst additionally an alkyl moiety in the abovementioned groups may be substituted by a carboxy, C-3-alkoxycarbonyl or phenyl group or in the 2 or 3 position by a di-(C 1 3 -alkyl)-amino, piperazino, N-(Cl- 3 -alkyl)-piperazino or 5- to 7-membered cycloalkyleneimino group, by a C 1 3 -alkyl group which is substituted by an amino, C,.,-alkylamino, C 5 ,-cycloalkylamino or phenyl-

C,

3 -alkylamino group which may additionally be substituted at the amino nitrogen atom by a C 13 -alkyl group wherein the hydrogen atoms are wholly or partially 4 replaced by fluorine atoms, by a Cs._-cycloalkyl,

C

2 4 -alkenyl or C 1 _4-alkyl group, whilst the abovementioned C.

4 -alkyl substituent may in each case be additionally mono-, di- or trisubstituted by a cyano, carboxy, C 1 _3-alkoxycarbonyl, pyridyl, imidazolyl, benzo[l,3]dioxole or phenyl group, wherein the phenyl group may be substituted by fluorine, chlorine or bromine atoms, by methyl, methoxy, trifluoromethyl, cyano or nitro groups and the substituents may be identical or different, or may be substituted in the 2, 3 or 4 position by a hydroxy group, by a C 13 -alkyl group which may be substituted by a hydroxy, carboxy, thiomorpholino, 1-oxidothiomorpholino, 1,1-dioxido-thiomorpholino, piperazino,

N-(C_

3 -alkyl)-piperazino or N-phenyl-piperazino group, by a 5- to 7-membered cycloalkenyleneimino group or by a 4- to 7-membered cycloalkyleneimino group, wherein the abovementioned 5- to 7-membered cycloalkyleneimino groups may be substituted by one or two C 1 _3-alkyl groups, by a C,_-cycloalkyl or phenyl group, by a

C

1 .3-alkyl, C_,-cycloalkyl, phenyl, carboxy or

C

1 _4-alkoxy-carbonyl group and by a hydroxy group and in the abovementioned cycloalkyleneimino groups a methylene group adjacent to the nitrogen atom may be replaced by a carbonyl group, by a C 13 -alkyl group which is substituted by a 5- to 7membered cycloalkyleneimino group, whilst a phenyl group optionally mono- or disubstituted by fluorine, chlorine or bromine atoms or by methyl or methoxy groups, wherein the substituents may be identical or different, or an oxazolo, imidazolo, thiazolo, pyridino, pyrazino or pyrimidino group, optionally substituted by a fluorine, chlorine, bromine or iodine atom or by a methyl, methoxy 5 or amino group, may be fused to the abovementioned 5- to 7-membered cycloalkyleneimino groups via two adjacent carbon atoms, whilst additionally the abovementioned monosubstituted phenyl groups may be substituted by a fluorine, chlorine or bromine atom or by a methyl, methoxy or nitro group, a 5-membered heteroaromatic group which contains an imino group, an oxygen or sulphur atom or an imino group, an oxygen or sulphur atom and one or two nitrogen atoms, or a 6-membered heteroaromatic group which contains one, two or three nitrogen atoms, whilst the abovementioned 5- and 6-membered heteroaromatic groups may additionally be substituted by a chlorine or bromine atom or by a methyl group, or a phenyl ring may be fused to the abovementioned or 6-membered heteroaromatic groups via two adjacent carbon atoms, and

R

s denotes a hydrogen atom or a C 13 -alkyl group.

Furthermore, the carboxy, amino or imino groups present in a compound of the above general formula I may be substituted by groups which can be cleaved in vivo.

In addition to the alkoxycarbonyl and alkanoyl groups already mentioned above, groups which can be cleaved in vivo include an acyl group such as the benzoyl, pyridinoyl, pentanoyl or hexanoyl group, an allyloxycarbonyl group, a

C

1 _g 1 -alkoxycarbonyl group such as the pentoxycarbonyl, hexyloxycarbonyl, octyloxycarbonyl, nonyloxycarbonyl, decyloxycarbonyl, undecyloxycarbonyl, dodecyloxycarbonyl or hexadecyloxycarbonyl group, a phenyl-C _6-alkoxycarbonyl group such as the benzyloxycarbonyl, phenylethoxycarbonyl or phenylpropoxycarbonyl group, a C 1 3 -alkylsulphonyl-C 24 6 alkoxycarbonyl, C, 3 -alkoxy-C 2 _,-alkoxy-C 2 4 -alkoxycarbonyl or RcCO-O- (RdCRe)-O-CO-group wherein

R

e denotes a C 1 8 alkyl, Cs_--cycloalkyl, phenyl or phenyl-

C-_

3 -alkyl group, Re denotes a hydrogen atom, a C 1 3 -alkyl, Cs-_-cycloalkyl or phenyl group and Rd denotes a hydrogen atom or a C 1 3 -alkyl group or the RcCO-O- (RdCRe) group, whilst the abovementioned ester groups may also be used as a group which can be converted in vivo into a carboxy group.

Preferred compounds of general formula I, however, are those wherein X denotes an oxygen atom, R, denotes a hydrogen atom,

R

2 denotes an aminocarbonyl group,

R

3 denotes a hydrogen atom or a C 1 4 -alkyl group which may be substituted, at the 2 position in relation to the carbon atom of the R 3

-C(R

4 NRs)= group by a chlorine or bromine atom or by a phenylsulphonyl group,

R

4 denotes a hydrogen atom, a C 1 3 -alkyl group or a cyclopentyl or cyclohexyl group optionally substituted by a methyl group, whilst in the cyclopentyl and cyclohexyl group a methylene group in the 3 or 4 position in relation to the carbon atom of the R 3

-C(R

4 NRs)= group may be replaced by an imino group optionally substituted by a methyl group, 7 a phenyl group which is substituted by a fluorine, chlorine, bromine or iodine atom, by a methoxy group optionally substituted by 1 to 3 fluorine atoms, by a C 2 -3-alkoxy which is substituted in the 2 or 3 position by methylamino, dimethylamino or 5- to 7membered cycloalkyleneimino group, whilst additionally a methyl group in the abovementioned amino groups may be substituted by a phenyl group, by a trifluoromethyl, amino,

N-(C

1 3

C

1 _s-alkylsulphonylamino, N- (C_ 3 -alkyl)-

C_,

5 -alkylsulphonylamino, phenylsulphonylamino,

N-(C

1 .3-alkyl)-phenylsulphonylamino or aminosulphonyl group, whilst additionally an alkyl moiety in the abovementioned alkylamino and dialkylamino groups may be substituted by a phenyl group, by a carbonyl group which is substituted by a hydroxy,

C_

3 -alkoxy, amino, C_.3-alkylamino or N- (C 1 5 -alkyl)-

C

1 3 -alkylamino group, whilst additionally an alkyl moiety in the abovementioned groups may be substituted by a carboxy, C,_ 3 -alkoxycarbonyl or phenyl group or in the 2 or 3 position by a di-(C 1 3 -alkyl)-amino, piperazino, N-(Cl--alkyl)-piperazino or 5- to 7-membered cycloalkyleneimino group, by a CI.3-alkyl group which is substituted by an amino,

C,_

7 -alkylamino, Cs_ 7 -cycloalkylamino or phenyl-

C

1 .3-alkylamino group which may additionally be substituted at the amino nitrogen atom by a C.--alkyl group wherein the hydrogen atoms are wholly or partially r 8 replaced by fluorine atoms, by a cyclohexyl, C 2 4 -alkenyl or C 1 _4-alkyl group, whilst the abovementioned C, 4 -alkyl substituent may in each case be additionally substituted by a cyano, carboxy, Cz_ 3 -alkoxycarbonyl, pyridyl, imidazolyl, benzo[l,3]dioxole or phenyl group, wherein the phenyl group may be monosubstituted by a fluorine, chlorine or bromine atom or by a methyl, methoxy, cyano, trifluoromethyl or nitro group, or di- or trisubstituted by fluorine, chlorine or bromine atoms or by methyl or methoxy groups, and the substituents may be identical or different, or may be substituted in the 2, 3 or 4 position by a hydroxy group, by a C 13 -alkyl group which may be substituted by a hydroxy, carboxy, thiomorpholino, 1-oxidothiomorpholino, 1,1-dioxido-thiomorpholino, piperazino,

N-(C_

3 -alkyl)-piperazino or N-phenyl-piperazino group, by a 5- to 7-membered cycloalkenyleneimino group or by a 4- to 7-membered cycloalkyleneimino group, wherein the abovementioned 5- to 7-membered cycloalkyleneimino groups may be substituted by one or two C, 3 -alkyl groups, by a cyclohexyl or phenyl group, by a C 1 3 -alkyl, cyclohexyl, phenyl, carboxy or C_4-alkoxy-carbonyl group and by a hydroxy group and in the abovementioned cycloalkyleneimino groups a methylene group adjacent to the nitrogen atom may be replaced by a carbonyl group, by a C 1 3 -alkyl group which is substituted by a 5- to 7membered cycloalkyleneimino group, whilst a phenyl group optionally mono- or disubstituted by fluorine, chlorine or bromine atoms or by methyl or methoxy groups, wherein the substituents may be identical or different, or a pyrazino or thiazolo group, optionally substituted by an amino group, may be fused to the abovementioned 5- to 7- 9 membered cycloalkyleneimino groups via two adjacent carbon atoms, whilst additionally the abovementioned monosubstituted phenyl groups may be substituted by a fluorine, chlorine or bromine atom or by a methyl, methoxy or nitro group, a pyridyl group optionally substituted by a chlorine or bromine atom or by a methyl group, an oxazolyl, isoxazolyl, imidazolyl or thiazolyl group optionally substituted by a methyl group, to which a phenyl ring may be fused via two adjacent carbon atoms, and

R

5 denotes a hydrogen atom or a C 13 -alkyl group, particularly those compounds of general formula I wherein RI to R 3 and R 5 are as hereinbefore defined and

R

4 denotes a hydrogen atom, a C 1 ._-alkyl group or a Cs,_-cycloalkyl group optionally substituted by a C 1 3 -alkyl group wherein a methylene group in the 3 or 4 position in relation to the carbon atom of the R 3

-C(R

4

NR

5 group may be replaced by an imino group optionally substituted by a

C

1 3 -alkyl group, a phenyl or naphthyl group which may be substituted by a fluorine, chlorine or iodine atom, by a C 13 -alkoxy, amino, C 1 .3-alkylamino, di- (C 1 _3-alkyl) -amino,

C

2 5 -alkanoylamino, N- (C 13 -alkylamino) -C2- 5 -alkanoylamino,

C

1 _s-alkylsulphonylamino, N-(C 13 -alkyl) C_.s-alkylsulphonylamino, phenylsulphonylamino or N-(C_,3-alkyl)-phenylsulphonylamino group or by a Ci_ 3 -alkyl group which may be substituted by a Cl.s-alkylamino, di-

(C

1 _s-alkyl)-amino, thiomorpholino, 1-oxido-thiomorpholino, 1,1-dioxido-thiomorpholino, piperazino, 3 -alkyl)- 9- 7-03:17:48 6/ 36 10 piperazino, N-phenyl-piperazino, Cs,-cycloalkenyleneimino group or by a C,.,-cycloalkyleneimino group, whilst the abovementioned Cs, 7 -cycloalkyleneimino groups may be substituted by one or two C,.,-alkyl groups, by a Cs- 7 -cycloalkyl or phenyl group, by a C,.--alkyl, Cs-,-cycloalkyl, phenyl, carboxy or Cz 4 -alkoxy-carbonyl group and by a hydroxy group, the stereoisomers and salts thereof.

Particularly preferred compounds of general formula I are those wherein -R to R. are as hereinbefore defined and R 2 is in the 5 position, 15 particularly those compounds wherein X denotes an oxygen atom, R, denotes a hydrogen atom,

R

2 in the 5 position denotes an aminocarbonyl group, R, denotes a hydrogen atom or a C, alkyl group which may be terminally substituted by a chlorine or bromine atom or S" 25 by a phenylsulphonyl.. group,

R

4 denotes a hydrogen atom, a C,--alkyl group or a cyclopentyl or cyclohexyl group optionally substituted by a methyl group, whilst in the cyclohexyl group a methylene group in the 4 position in relation to the carbon atom of the R 3

-C(R

4

NR

5 group may be replaced by an imino group optionally substituted by a methyl group, a phenyl group which may be substituted.

by a fluorine, chlorine, bromine or iodine atom, COMS ID No: SMBI-00327262 Received by IP Australia: Time 18:02 Date 2003-07-09 9- 7-03:17:48 7/ 36 11 by a methyl or ethyl' group, which may in each case be substituted by a C.3 -alkylamino, di- (C 1 .,-alkyl) -amino, thiomorpholino, 1-oxido-thiomorpholino, l,1-dioxidothiomorpholino, N-phenyl-piperazino, 5- to 6-membered cycloalkenyleneimino group or by a 5- to 7-membered cycloalkyleneimino group, whilst the abovementioned 5- to 7-membered cycloalkyleneimino groups may be substituted by one or two methyl groups, by a cyclohexyl or phenyl group, by a methyl, cyclohexyl or phenyl group and by a hydroxy group, or by a methyl or ethyl group which may be substituted by a phenyl group which is substituted by a 5 to 7-membered cycloalkyleneimino group, whilst additionally a phenyl ring is fused to the abovementioned cycloalkyleneimino groups via 2 adjacent carbon atoms, by a methyl or ethyl group substituted by an amino, methylamino or ethylamino group, each of which is additionally substituted at the amino nitrogen atom by a benzyl or phenylethyl group, wherein the phenyl moiety in the abovementioned groups may be monosubstituted by a fluorine, chlorine or bromine atom or by a methyl, 25 methoxy, cyano, trifluoromethyl or nitro group or di- or trisubstituted by fluorine, chlorine or bromine atoms or by methyl or methoxy groups, and the substituents may be identical or different, whilst additionally the abovementioned monosubstituted phenyl groups may be substituted by a fluorine, chlorine or bromine atom or by a methyl, methoxy or nitro group, and

R

s denotes a hydrogen atom or a C 1 .,-alkyl group, the stereoisomers and the salts thereof.

COMS ID No: SMBI-00327262 Received by IP Australia: Time 18:02 Date 2003-07-09 12 Most particularly preferred compounds of general formula I are those wherein X denotes an oxygen atom, RI denotes a hydrogen atom, R, in the 5 position denotes an aminocarbonyl group,

R

3 denotes a hydrogen atom or a C 14 -alkyl group,

R

4 denotes a phenyl group which may be substituted by a fluorine, chlorine, bromine or iodine atom, by a methyl or ethyl group, which may be substituted in each case by a C 1 3 -alkylamino, di-(C-_ 3 -alkyl)-amino, thiomorpholino, 1-oxido-thiomorpholino, 1,1-dioxidothiomorpholino, N-phenyl-piperazino, 5- to 6-membered cycloalkenyleneimino group or by a 5- to 7-membered cycloalkyleneimino group, whilst the abovementioned 5- to 7-membered cycloalkyleneimino groups may be substituted by one or two methyl groups, by a cyclohexyl or phenyl group, by a methyl, cyclohexyl or phenyl group and by a hydroxy group, or by a methyl or ethyl group which may be substituted by a phenyl group which is substituted in the 4 position by a to 7-membered cycloalkyleneimino group, whilst additionally a phenyl ring is fused to the abovementioned cycloalkyleneimino groups via 2 adjacent carbon atoms, by a methyl or ethyl group substituted by an amino, methylamino or ethylamino group, each of which is additionally substituted at the amino nitrogen atom by a benzyl or phenylethyl group, and wherein the phenyl moiety 9- 7-03;17!48 8/ 36 -13 may be monosubstituted by a fluorine, chlorine or bromine atom or by a methyl, methoxy, cyano, brifluoromethyl or nitro group, disubstituted by methyl or methoxy groups or trisubstituted by methyl. or methoxy groups, and the substituents may be identical or different, whilst additionally the abovementioned monosubstitute d phenyl groups may be substituted by a fluorine, chlorine or bromine atom or by a methyl, methoxy or nitro group, and R, denotes a hydrogen atom or a C,..-alkyl group, the stereoisOi'flrS and the salts thereof.

The following are mentioned as examples of particularly preferred compounds: Ca) 3-2- £1-(4-piperidinomethyl-phenylamino) -1-methyl-methyleni )-5-amido-2-indolinone, (4-bromo-phenylamino) -1-methyl-methylene] amido-2-indolinone, 3-2- [i-(4-piperidinomethyl-phenylaminio) -1-butylmethylene) -5-amiido-2-indolinone, 3-Z- [i-(4-chiorophenylanino) -1-methyl-methylene] amido- 2- indolinone and 3-Z- (l-phenylamino-methylene) -5-amido-2-indolinone 3-Z-11- (N-benzyl-N-methyl-aminomethyl) phenylamino) -1-methyl-methylene] -S-amido-2-indolinone, (4-chlorobenzyl) -aminomethyl) iphenylamino) -1-methyl-methylene] -5-amido-2-indolinone, COMS ID No: SMBI-00327262 Received by IP Australia: Time 18:02 Date 2003-07-09

C

9- 7-03:17:48 9/l 36 3 Z- [1 (4 (I-benzyl ethyl -aminomethyl) -phenylarninol 1-methyl -methyleneJ -5-amido-2-indolinone, (54 2-2- 11- (4-(N-benzyl-aminomethyl) -phenylamino)-2.methyl -methylene] -5-amido-2-indolinone, 3-Z-[l-(4-(N-benzyl-N-methyl-aminomethyl) phenylamino) -methyleneJ -5-amido-2-indolinone, CW 3-Z-li- (4-C2,3.4,5-tetrahydro-ben'zo(d)azepin-3-ylmethyl) -phenylanino) -1-met'hyl-methylene] -5-amido-2indolinone, 1s 2-Z- (4-piperidinomethyl-3-nitro-phenylamino) 1-methyl -methylene] -5-amido'-2-indolinone and (in) (4-methyl-3-nitro-phenylaino) -1-methylmethylene) -5-ainido-2-indolinone as well as the stersoisomers and the salts thereof.

According to the- inventilon, the new* compounds may be obtained, for example, according to the following processes 25 known in principle from the literature: a. reacting a compound of general f6rmula 6*

CC.

C -Z

I

(II)I

wherein COMS ID No: SMBI-00327262 Received by IP Australia: Time 18:02 Date 2003-07-09 15 X and R 3 are as hereinbefore defined,

R

2 has the meanings given for R 2 hereinbefore, R, denotes a hydrogen atom or a protecting group for the nitrogen atom of the lactam group, whilst one of the groups

R

2 or R 6 may also denote a bond to a solid phase optionally formed via a spacer and the other group R 2 or R 6 is as hereinbefore defined, and Z denotes a halogen atom, a hydroxy, alkoxy or aralkoxy group, e.g. a chlorine or bromine atom or a methoxy, ethoxy or benzyloxy group, with an amine of general formula /Rs H N (III), R4 wherein

R

4 and Rs are as hereinbefore defined, and if necessary subsequently cleaving any protecting groups used for the nitrogen atom of the lactam group or from a solid phase.

A suitable protecting group for the nitrogen atom of the lactam group might be, for example, an acetyl, benzoyl, ethoxycarbonyl, tert.butyloxycarbonyl or benzyloxycarbonyl group and A suitable solid phase might be, for example, a resin such as a 4-(2',4'-dimethoxyphenylaminomethyl)-phenoxy resin, the bonding preferably taking place via the amino group, or a p-benzyloxybenzylalcohol resin, the bonding preferably taking place via an intermediate member such as a dimethoxy-4-hydroxy-benzyl derivative.

The reaction is appropriately carried out in a solvent such as dimethylformamide, toluene, acetonitrile, 16 tetrahydrofuran, dimethylsulphoxide, methylene chloride or mixtures thereof, optionally in the presence of an inert base such as triethylamine, N-ethyl-diisopropylamine or sodium hydrogen carbonate at temperatures between 20 and 175 0 C, whilst any protecting group used may be cleaved at the same time as a result of transamidation.

If Z in a compound of general formula II denotes a halogen atom, the reaction is preferably carried out in the presence of an inert base at temperatures of between and 120 0

C.

If Z i in a compound of general formula II denotes a hydroxy, alkoxy or aralkoxy group, the reaction is preferably carried out at temperatures between 20 and 200°C.

The subsequent cleaving of any protecting group used, if necessary, is appropriately carried out either hydrolytically in an aqueous or alcoholic solvent, e.g. in methanol/water, ethanol/water, isopropanol/water, tetrahydrofuran/water, dioxan/water, dimethylformamide/water, methanol or ethanol in the presence of an alkali metal base such as lithium hydroxide, sodium hydroxide or potassium hydroxide at temperatures between 0 and 100 0 C, preferably at temperatures between 10 and 50 0

C,

or more advantageously by transamidation with an organic base such as ammonia, methylamine, butylamine, dimethylamine or piperidine in a solvent such as methanol, ethanol, dimethylformamide and mixtures thereof or in an excess of the amine used, at temperatures of between 0 and 100 0 C, preferably at temperatures between 10 and 50 0

C.

17 Any solid phase used is preferably cleaved by means of trifluoroacetic acid and water at temperatures of between 0 and 35 0 C, preferably at ambient temperatures.

b. in order to prepare a compound of general formula I wherein R 2 denotes one of the abovementioned aminocarbonyl groups: amidating a compound of general formula

R

3 HO-CO 0 (IV)

RI

wherein R i and R 3 are as hereinbefore defined, or the reactive derivatives thereof, with an amine of general formula H (R 7

NR

8

(V)

wherein R 7 and R 8 which may be identical or different denote hydrogen atoms or C 1 3 -alkyl groups.

The amidation is preferably carried out in a solvent such as methylene chloride, diethyl ether, tetrahydrofuran, toluene, dioxan, acetonitrile, dimethylsulphoxide or dimethylformamide, optionally in the presence of an inorganic or tertiary organic base, preferably at temperatures between 20 0 C and the boiling temperature of the solvent used. The amidation is carried out with a 18 corresponding acid, preferably in the presence of a dehydrating agent, e.g. in the presence of isobutyl chloroformate, tetraethyl orthocarbonate, trimethyl orthoacetate, 2,2-dimethoxypropane, tetramethyloxysilane, thionylchloride, trimethylchlorosilane, phosphorus trichloride, phosphorus pentoxide, N,N'dicyclohexylcarbodiimide, N,N'-dicyclohexylcarbodiimide/Nhydroxysuccinimide, N,N'-dicyclohexylcarbodiimide/lhydroxy-benzotriazole, 2-(1H-benzotriazol-l-yl)-1,1,3,3tetramethyluronium tetrafluoroborate, 2-(1H-benzotriazoll-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate/1hydroxy-benzotriazole, N,N'-carbonyldiimidazole or triphenylphosphine/carbon tetrachloride, and optionally with the addition of a base such as pyridine, 4dimethylaminopyridine, N-methylmorpholine or triethylamine, appropriately at temperatures between 0 and 150 0 C, preferably at temperatures between 0 and 100 0 C, and the acylation is carried out with a corresponding reactive compound such as the anhydride, ester, imidazolide or halide thereof, optionally in the presence of a tertiary organic base such as triethylamine, Nethyldiisopropylamine or N-methylmorpholine at temperatures between 0 and 150 0 C, preferably at temperatures between 50 and 100°C.

If according to the invention a compound of general formula I is obtained which contains an alkoxycarbonyl group, this may be converted by hydrolysis into a corresponding carboxy compound, or if a compound of general formula I is obtained which contains an amino or alkylamino group, this may be converted by alkylation or reductive alkylation into a corresponding alkylamino or dialkylamino compound, or (1 19 if a compound of general formula I is obtained which contains an amino or alkylamino group, this may be converted by acylation into a corresponding acyl compound, or if a compound of general formula I is obtained which contains a carboxy group, this may be converted by esterification or amidation into a corresponding ester or aminocarbonyl compound, or if a compound of general formula I is obtained which contains a nitro group, this may be converted by reduction into a corresponding amino compound.

The subsequent hydrolysis is preferably carried out in an aqueous solvent, e.g. in water, isopropanol/water, tetrahydrofuran/water or dioxan/water, in the presence of an acid such as trifluoroacetic acid, hydrochloric acid or sulphuric acid or in the presence of an alkali metal base such as lithium hydroxide, sodium hydroxide or potassium hydroxide at temperatures between 0 and 100 0 C, preferably at temperatures between 10 and 50 0

C.

The subsequent reductive alkylation is preferably carried out in a suitable solvent such as methanol, methanol/water, methanol/water/ammonia, ethanol ether, tetrahydrofuran, dioxan or dimethylformamide, optionally with the addition of an acid such as hydrochloric acid in the presence of catalytically activated hydrogen, e.g.

hydrogen in the presence of Raney nickel, platinum or palladium/charcoal, or in the presence of a metal hydride such as sodium borohydride, lithium borohydride or lithium aluminium hydride at temperatures between 0 and 100°C, preferably at temperatures between 20 and 80 0

C.

20 The subsequent alkylation is carried out with an alkylating agent such as an alkyl halide or dialkylsulphate such as methyl iodide, dimethylsulphate or propyl bromide, preferably in a solvent such as methanol, ethanol, methylene chloride, tetrahydrofuran, toluene, dioxan, dimethylsulphoxide or dimethylformamide, optionally in the presence of an inorganic or tertiary organic base such as triethylamine, N-ethyldiisopropylamine or dimethylaminopyridine, preferably at temperatures between 20 0 C and the boiling temperature of the solvent used.

The subsequent acylation is preferably carried out in a solvent such as methylene chloride, diethyl ether, tetrahydrofuran, toluene, dioxan, acetonitrile, dimethylsulphoxide or dimethyl formamide, optionally in the presence of an inorganic or tertiary organic base, preferably at temperatures between 20 0 C and the boiling temperature of the solvent used. The acylation is carried out with a corresponding acid, preferably in the presence of a dehydrating agent, e.g. in the presence of isobutyl chloroformate, tetraethyl orthocarbonate, trimethyl orthoacetate, 2,2-dimethoxypropane, tetramethoxysilane, thionylchloride, trimethylchlorosilane, phosphorus trichloride, phosphorus pentoxide, N,N'dicyclohexylcarbodiimide, N,N'-dicyclohexylcarbodiimide/Nhydroxysuccinimide, N,N'-dicyclohexylcarbodiimide/lhydroxy-benzotriazole, 2-(1H-benzotriazol-l-yl)-1,1,3,3tetramethyluronium tetrafluoroborate, 2-(1H-benzotriazoll-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate/1hydroxy-benzotriazole, N,N'-carbonyldiimidazole or triphenylphosphine/carbon tetrachloride, and optionally with the addition of a base such as pyridine, 4dimethylamino-pyridine, N-methylmorpholine or triethylamine, appropriately at temperatures of between 0 and 150 0 C, preferably at temperatures of between 0 and 21 100 0 C, and the acylation is carried out with a corresponding reactive compound such as an anhydride, ester, imidazole or halide thereof, optionally in the presence of a tertiary organic base such as triethylamine, N-ethyl-diisopropylamine or N-methyl-morpholine at temperatures of between 0 and 150 0 C, preferably at temperatures of between 50 and 100 C.

The subsequent esterification or amidation is appropriately carried out by reacting a corresponding reactive carboxylic acid derivative with a corresponding alcohol or amine as described hereinbefore.

The subseqent reduction of a nitro group is preferably carried out by hydrogenolysis, e.g. with hydrogen in the presence of a catalyst such as palladium/charcoal or Raney nickel in a solvent such as methanol, ethanol, ethyl acetate, dimethylformamide, dimethylformamide/acetone or glacial acetic acid, optionally with the addition of an acid such as hydrochloric acid or glacial acetic acid at temperatures between 0 and 50 0 C, but preferably at ambient temperature, and at a hydrogen pressure of from 1 to 7 bar, but preferably from-3 to 5 bar.

In the reactions described hereinbefore, any reactive groups present such as carboxy, amino, alkylamino or imino groups may be protected during the reaction by conventional protecting groups which are cleaved again after the reaction.

For example, a protecting group for a carboxy group may be a trimethylsilyl, methyl, ethyl, tert.butyl, benzyl or tetrahydropyranyl group and protecting groups for an amino, alkylamino or imino group may be an acetyl, trifluoroacetyl, benzoyl, ethoxycarbonyl, tert.butoxycarbonyl, benzyloxycarbonyl, 22 benzyl, methoxybenzyl or 2,4-dimethoxybenzyl group and additionally, for the amino group, a phthalyl group.

Any protecting group used is optionally subsequently cleaved for example by hydrolysis in an aqueous solvent, e.g. in water, isopropanol/water, tetrahydrofuran/water or dioxan/water, in the presence of an acid such as trifluoroacetic acid, hydrochloric acid or sulphuric acid or in the presence of an alkali metal base such as lithium hydroxide, sodium hydroxide or potassium hydroxide, at temperatures between 0 and 100 0 C, preferably at temperatures between 10 and 50 0

C.

However, a benzyl, methoxybenzyl or benzyloxycarbonyl group is cleaved, for example hydrogenolytically, e.g.

with hydrogen in the presence of a catalyst such as palladium/charcoal in a suitable solvent such as methanol, ethanol, ethyl acetate, dimethylformamide, dimethylformamide/acetone or glacial acetic acid, optionally with the addition of an acid such as hydrochloric acid or glacial acetic acid at temperatures between 0 and 50 0 C, but preferably at ambient temperature, and at a hydrogen pressure of 1 to 7 bar, but preferably 3 to 5 bar.

A methoxybenzyl group may also be cleaved in the presence of an oxidising agent such as cerium(IV)ammonium nitrate in a solvent such as methylene chloride, acetonitrile or acetonitrile/water at temperatures of between 0 and 50 0

C,

preferably at ambient temperature.

A 2,4-dimethoxybenzyl group, however, is preferably cleaved in trifluoroacetic acid in the presence of anisole.

A tert.butyl or tert.butyloxycarbonyl group is preferably cleaved by treating with an acid such as trifluoroacetic

LI

23 acid or hydrochloric acid, optionally using a solvent such as methylene chloride, dioxan, ethyl acetate or ether.

A phthalyl group is preferably cleaved in the presence of hydrazine or a primary amine such as methylamine, ethylamine or n-butylamine in a solvent such as methanol, ethanol, isopropanol, toluene/water or dioxan at temperatures between 20 and 50 0

C.

Moreover, chiral compounds of general formula I obtained may be resolved into their enantiomers and/or diastereomers: Thus, for example, the compounds of general formula I obtained which occur as racemates may be separated by methods known per se (cf. Allinger N. L. and Eliel E. L.

in "Topics in Stereochemistry", Vol. 6, Wiley Interscience, 1971) into their optical antipodes and compounds of general formula I with at least 2 asymmetric carbon atoms may be resolved into their diastereomers on the basis of their physical-chemical differences using methods known per se, e.g. by chromatography and/or fractional crystallisation, and, if these compounds are obtained in racemic form, they may subsequently be resolved into the enantiomers as mentioned above.

The enantiomers are preferably separated by column separation on chiral phases or by recrystallisation from an optically active solvent or by reacting with an optically active substance which forms salts or derivatives such as e.g. esters or amides with the racemic compound, particularly acids and the activated derivatives or alcohols thereof, and separating the diastereomeric mixture of salts or derivatives thus obtained, e.g. on the basis of their differences in solubility, whilst the free antipodes may be released from the pure diastereomeric 24 salts or derivatives by the action of suitable agents.

Optically active acids in common use are e.g. the D- and L-forms of tartaric acid or dibenzoyltartaric acid, dio-tolyltartaric acid, malic acid, mandelic acid, camphorsulphonic acid, glutamic acid, aspartic acid, Nacetyl-aspartic acid or quinic acid. An optically active alcohol may be for example or (-)-menthol and an optically active acyl group in amides, for example, may be a or (-)-menthyloxycarbonyl group.

Furthermore, the compounds of formula I may be converted into the salts thereof, particularly for pharmaceutical use into the physiologically acceptable salts with inorganic or organic acids. Acids which may be used for this purpose include for example hydrochloric acid, hydrobromic acid, sulphuric acid, phosphoric acid, fumaric acid, succinic acid, lactic acid, citric acid, tartaric acid, maleic or methanesulphonic acid.

Moreover, if the new compounds of formula I contain a carboxy group, they may subsequently, if desired, be converted into the salts thereof with inorganic or organic bases, particularly for pharmaceutical use into the physiologically acceptable salts thereof. Suitable bases for this purpose include for example sodium hydroxide, potassium hydroxide, arginine, cyclohexylamine, ethanolamine, diethanolamine and triethanolamine.

The compounds of general formulae I to V used as starting materials are known from the literature in some cases or are described in the Examples.

As already mentioned, the new compounds of general formula I wherein R i denotes a hydrogen atom or a prodrug group have valuable pharmacological properties, particularly an inhibitory effect on various kinases and cycline/CDK complexes, on the proliferation of cultivated human tumour 25 cells and, when administered orally, on the growth of tumours in nude mice which have been infected with human tumour cells.

For example, the compounds listed in Table 1 were tested for their biological properties as follows: Test 1 Inhibition of cycline/CDK enzyme, in vitro activity High Five T insect cells (BTI-TN-5B1-4) which had been infected with a high titre of recombinant baculovirus were used to produce active human cycline/CDK holoenzymes. By using a baculovirus vector which contained two promoters (polyhedrin enhancer promoter, P10 enhancer promoter), GST-tagged cyclines cycline D1 or cycline D3) with the corresponding His 6 -tagged CDK subunit for CDK4 or CDK6) were expressed in the same cell. The active holoenzyme was isolated by affinity chromatography on glutathione sepharose. Recombinant GST-tagged pRB (aa 379-928) was produced in E. coli and purified by affinity chromatography on glutathione sepharose.

The substrates used for the kinase assays depended on the specific kinases. Histone H1 (Sigma) was used as the substrate for cycline E/CDK2, cycline A/CDK2, cycline B/CDK1 and for v-cycline/CDK6. GST-tagged pRB (aa 379- 928) was used as substrate for cycline D1/CDK4, cycline D3/CDK4, cycline D1/CDK6 and for cycline D3/CDK6.

Lysates of the insect cells infected with recombinant baculovirus or recombinant kinases (obtained from the lysates by purification) were incubated together with radiolabelled ATP in the presence of a suitable substrate with various concentrations of the inhibitor in a 1% DMSO (dimethyl sulphoxide) solution for 45 minutes at 30 0

C.

26 The substrate proteins with associated radioactivity were precipitated with 5% TCA (trichloroacetic acid) in waterrepellent PVDF multi-well microtitre plates (Millipore) or with 0.5% phosphoric acid solution on Whatman P81 filters.

After the addition of scintillation liquid the radioactivity was measured in a Wallace 1450 Microbeta Liquid Scintillation Counter. For each concentration of the substance double measurements were carried out; IC, 0 values were calculated for the enzyme inhibition.

Test 2 Inhibition of the proliferation of cultivated human tumour cells Cells of the Leiomyosarcoma tumour cell line SK-UT-1B (obtained from the American Type Culture Collection (ATCC)) were cultivated in Minimum Essential Medium with non-essential amino acids (Gibco), supplemented with sodium pyruvate (1 mmol), glutamine (2 mmol) and foetal calf serum (Gibco) and harvested during the loggrowth phase. Then the SK-UT-1B cells were added to Cytostar® multi-well plates (Amersham) at a density of 4000 cells per well and incubated overnight in an incubator. Various concentrations of the compounds (dissolved in DMSO; final concentration: were added to the cells. After 48 hours' incubation "C-thymidine (Amersham) was added to each well and incubation was continued for a further 24 hours. The quantity of 14

C

thymidine incorporated into the tumour cells in the presence of the inhibitor and representing the number of cells in the S phase was measured in a Wallace 1450 Microbeta Liquid Scintillation Counter. IC 0 values for the inhibition of proliferation inhibition of incorporated "C-thymidine) were calculated, correcting for the background radiation. All the measurements were done twice.

27 Test 3 In vivo effects on tumour-bearing nude mice 106 cells [SK-UT-1B, or non-small cell lung tumour NCI- H460 (obtained from ATCC)] in a volume of 0.1 ml were injected subcutaneously into male and/or female nude mice (NMRI nu/nu; 25-35g; N 10-20); alternatively, small fragments of SK-UT-1B or NCI-H460 cell clumps were implanted subcutaneously. One to three weeks after the injection or implantation a kinase inhibitor was administered daily by oral route for a period of 2 to 4 weeks (by oesophageal tube). The size of the tumour was measured three times a week using a digital sliding gauge.

The effect of a kinase inhibitor on the tumour growth was determined as a percentage inhibition compared with a control group treated with placebo.

Table 2 which follows contains the results obtained in in vitro test 2: 28 Compound Inhibition of SKUT (example no.) -1B proliferation

IC,

0

[IM]

1(11) 0.032 1(8) 0.060 1(26) 0.036 1(3) 0.040 1(1) 0.100 1(96) 0.005 1(91) 0.010 1(95) 0.008 1(51) 0.013 1(105) 0.019 1(110) 0.020 1(117) 0.020 1(71) 0.030 In view of their biological properties, the new compounds of general formula I, their isomers and physiologically acceptable salts are suitable for the treatment of diseases characterised by excessive or abnormal cell proliferation.

Such diseases include (with no claim to completeness): viral infections HIV and Kaposi's sarcoma); inflammation and autoimmune diseases colitis, arthritis, Alzheimer's disease, glomerulonephritis and wound healing); bacterial, fungal and/or parasitic infections; leukaemias, lymphoma and solid tumours; skin diseases psoriasis); bone diseases; cardiovascular diseases restenosis and hypertrophy). They are also useful for protecting proliferating cells hair, intestinal, blood and progenitor cells) against DNA damage caused by radiation, UV treatment and/or cytostatic treatment.

29 The new compounds may be used for the short-term or longterm treatment of the abovementioned diseases, optionally in conjunction with other 'state of the art' compounds such as other cytostatics.

The dosage required to achieve such an effect is appropriately 0.1 to 30 mg/kg, preferably 0.3 to 10 mg/kg by intravenous route, and 0.1 to 100 mg/kg, preferably 0.3 to 30 mg/kg by oral route, in each case administered 1 to 4 times a day. For this purpose, the compounds of formula I prepared according to the invention may be formulated, optionally together with other active substances, with one or more inert conventional carriers and/or diluents, e.g.

with corn starch, lactose, glucose, microcrystalline cellulose, magnesium stearate, polyvinylpyrrolidone, citric acid, tartaric acid, water, water/ethanol, water/glycerol, water/sorbitol, water/polyethylene glycol, propylene glycol, cetylstearyl alcohol, carboxymethylcellulose or fatty substances such as hard fat or suitable mixtures thereof, to produce conventional galenic preparations such as plain or coated tablets, capsules, powders, suspensions or suppositories.

The Examples which follow are intended to illustrate the invention: 30 Example I Methyl 1-acetyl-2-indolinone-5-carboxylate 10.5 g of methyl 2-indolinone-5-carboxylate (prepared analogously to Ogawa, Hidenori et al. in Chem.Pharm.Bull 36, 2253-2258 (1988)) are stirred in 30 ml of acetic anhydride for 4 hours at 140 0 C. The mixture is then left to cool, poured onto ice water and the precipitate is suction filtered. The product is washed with water once more, then taken up in methylene chloride, dried over sodium sulphate and concentrated by evaporation.

Yield: 11 g (86 of theory), Rf value: 0.63 (silica gel, methylene chloride/methanol 50:1) Example II Methyl l-acetyl-3-(l-ethoxy-l-butyl-methylene]-2- 11 g of methyl l-acetyl-2-indolinone-5-carboxylate are stirred in 110 ml of acetic anhydride and 30 ml of triethyl orthovalerate for 2 hours at 100 0 C. Then it is concentrated by rotary evaporation, the residue is washed with ether and suction filtered.

Yield: 11.5 g (67 of theory), Revalue: 0.55 (silica gel, methylene chloride/petroleum ether/ethyl acetate 4:5:1) The following compounds are prepared analogously to Example II: methyl l-acetyl-3-(1-ethoxy-methylene]-2-indolinone-5carboxylate Prepared from methyl and trimethyl orthoformate 31 methyl l-acetyl-3-(l-ethoxy-l-methyl-methylene]-2- Prepared from methyl and triethyl orthoacetate methyl l-acetyl-3-(l-ethoxy-l-ethyl-methylene]-2- Prepared from methyl and triethyl orthopropionate Example III 28.0 g of Rink resin (MBHA resin made by Novobiochem) were allowed to swell in 330 m of dimethylformamide. Then 330 ml of 30% piperidine in dimethyl formamide were added and the mixture was shaken for 7 minutes to cleave the 9Hfluoren-9-yl-methoxycarbonyl group. Then the resin was washed several times with dimethylformamide. Finally, 7.3 g 10.5 g of 2-indolinone-5-carboxylic acid (prepared analogously to Ogawa, Hidenori et al., Chem. Pharm. Bull 36, 2253-2258 (1988)), 5.6 g of hydroxybenzotriazole, 13.3 g of O-(benzotriazol-l-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate and 5.7 ml of N-ethyl-diisopropylamine in 300 ml of dimethylformamide were added and the mixture was shaken for 1 hour. The solution was suction filtered and the resin was washed five times with 300 ml of dimethylformamide and three times with 300 ml of methylene chloride. To dry it, nitrogen was blown through the resin.

Yield: 20 g of charged resin Example IV 0.4 g of the charged resin prepared in Example III were stirred with 2.5 ml of acetic anhydride at 90°C for 1 hour. Then 2.5 ml of trimethyl orthovalerate were added and the mixture was shaken for a further 3 hours at 110 0

C.

32 Then the resin was suction filtered and washed with dimethylformamide, methanol and finally with methylene chloride.

Yield: 0.6 g of moist resin The following charged resins were prepared analogously to Example IV: resin charged with 3-Z-(l-ethoxy-methylene)-5-amido-2indolinone by reacting the product of Example I and triethyl orthoformate resin charged with 3-Z-(1-methoxy-l-methyl-methylene)- 5-amido-2-indolinone by reacting the product of Example I and trimethyl orthoformate resin charged with amido-2-indolinone by reacting the product of Example I and trimethyl orthopropionate resin charged with 3-Z-(l-methoxy-l-propyl-methylene)- 5-amido-2-indolinone by reacting the product of Example I and trimethyl orthobutyrate resin charged with 3-Z-(l-methoxy-l-ethenyl-methylene)- 5-amido-2-indolinone by reacting the product of Example I and 3,3,3-triethoxyprop-l-ene resin charged with 3-Z-(l-methoxy-l-(3-bromo-propyl)methylene)-5-amido-2-indolinone by reacting the product of Example I and trimethyl 4-bromo-orthobutyrate resin charged with 3-Z-(l-methoxy-l-(2-phenylsulphonylethyl)-methylene)-5-amido-2-indolinone by reacting the product of Example I and triethyl 3-phenylsulphonylorthopropionate 33 Example V 4-(N-Ethyl-aminomethyl)-nitrobenzene 6 g of 4-nitrobenzylbromide are dissolved in 25 ml of ethanol, mixed with 25 ml of 10% ethanolic ethylamine solution and refluxed for 2 hours. Then the solution is concentrated by rotary evporation, the residue is taken up in methylene chloride and washed with dilute sodium hydroxide solution. Then the organic phase is concentrated by evaporation.

Yield: 2.3 g (-46 of theory), Revalue: 0.20 (silica gel, methylene chloride/methanol 9:1) The following compounds are prepared analogously to Example V: 4-[N-(4-chlorophenyl-methyl)-aminomethyl]-nitrobenzene 4-(N-cyclohexyl-aminomethyl)-nitrobenzene 4-(N-isopropyl-aminomethyl)-nitrobenzene 4-(N-butyl-aminomethyl)-nitrobenzene 4-(N-methoxycarbonylmethyl-aminomethyl)-nitrobenzene 4-(N-benzyl-aminomethyl)-nitrobenzene 4-(pyrrolidino-methyl)-nitrobenzene 4-(morpholino-methyl)-nitrobenzene 4-(piperidino-methyl)-nitrobenzene.

4-(hexamethyleneimino-methyl)-nitrobenzene 34 4- (4-hydroxy-piperidino-methyl) -nitrobenzene 4- (4-methyl -piperidino-methyl) -nitrobenzene 4- (4-ethyl -piperidino-methyl) -nitrobenzene 4- (4-isopropyl-piperidino-methyl) -nitrobenzene 4- (4-phenyl-piperidino-methyl) -nitrobenzene 4- (4-benzyl -piperidino-methyl) -nitrobenzene 4- (4-ethoxycarbonyl-piperidino-methyl) -nitrobenzene 4- (dimethylamino-methyl) -nitrobenzene 4- (di-n-propylamino-methyl) -nitrobenzene 4- (4-tert .butoxycarbonyl-piperazino-methyl) -nitrobenzene 3- (direthylamino-methyl) -nitrobenzene 4- (2-diethylamino-ethyl) -nitrobenzene 4- (2-morpholino-ethyl) -nitrobenzene 4- (2-pyrrolidino-ethyl) -nitrobenzene 4- (2-piperidino-ethyl) -nitrobenzene 4- (N-ethyl-N-benzyl-aminomethyl) -nitrobenzene 4- (N-n-propyl-N-benzyl-aminomethyl) -nitrobenzene 4- [N-methyl-N- (4-chlorophenylmethyl) -aminomethyl] nitrobenzene 35 4- [N-methyl-N- (4-bromophenylmethyl) -aminomethyl] nitrobenzene 4- [N-methyl-N- (3-chiorophenylmethyl) -aminomethyl] nitrobenzene 4- [N-methyl-N- (3,4-dimethoxyphenylmethyl) -aminomethyl] nitrobenzene 4- [N-methyl-N- (4-methoxyphenylmethyl) -aminomethyl) nitrobenzene 4-EN- (2,2,2-trifluoroethyl) -N-benzyl-aminomethyl] nitrobenzene 4- (2,2,2-trifluoroethyl) (4-chiorophenylmethyl) aminomethyl] -nitrobenzene 4- 6-dimethyl-piperidino-methyl) -nitrobenzene 4- (thiomorpholino-methyl) -nitrobenzene 4- (S-oxido-thiomorpholino-methyl) -nitrobenzene 4- S-dioxido-thiomorpholino-methyl) -nitrobenzene 4- (azetidino-methyl) -nitrobenzene 4- 5-dihydropyrrol-l-yl-methyl) -nitrobenzene 4- (3,6-dihydro-2H-pyridin-l-yl-methyl) -nitrobenzene 4- (2-methoxycarbonyl-pyrrolidino-methyl) -nitrobenzene 4- 5-dimethyl-piperidino-methyl) -nitrobenzene 36 4- (4-phenyl-piperazinyl-methyl) -nitrobenzene 4- (4-phenyl-4-hydroxy-piperidino-methyl) -nitrobenzene 4- (3,4,5-trimethoxy-beizyl) -N-methyl-aminomethyl] nitrobenzene 4- 4-dimethoxy-benzyl) -N-ethyl-aminomethyl] nitrobenzene 4- (3-chlorobenzyl) -N-methyl-aminomethyl] -nitrobenzene 4- 6-dichlorobenzyl) -N-methyl-aminomethyl] nitrobenzene 4- (4-trifluoromethylbenzyl) -N-methyl-aminomethyl] nitrobenzene 4- (N-benzyl-N-isopropyl-aninomethyl) -nitrobenzene 4- (N-benzyl-N-tert .butyl-aminomethyl) -nitrobenzene 4- (diisopropylamino-methyl) -nitrobenzene 4- (di-n-propylamino-methyl) -nitrobenzene 4- (diisobutylamino-methyl) -nitrobenzene 4- (2,3,4,5-tetrahydro-benzo(d)azepin-3-yl-methyl) nitrobenzene 4- (2,3-dihydro-isoindol-2-yl-methyl) -nitrobenzene 4- (6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinolin-2-ylmethyl) -ritrobenzene 37 4- (1,2,3,4-tetrahydro-isoquinolin-2-yl-methyl) nitrobenzene 4- (2-hydroxyethyl) -N-benzyl-aminomethyl] -nitrobenzene 4- (1-ethyl-pentyl) (pyridin-2-yl-methyl) aminomethyl] -nitrobenzene 4- (N-phenethyl -N-methyl -aminomethyl) -nitrobenzene 4- (3,4-dihydroxy-phenethyl) -N-methyl-aminomethyl] nitrobenzene 4- IN- 5-trimethoxy-phenethyl) -N-methyl-aminomethyl] nitrobenzene 4- 4-dimethoxy-phenethyl) -N-methyl-aminomethyl] nitroberizene 4- (4-nitro-phenethyl) -N-methyl-aminomethyl] nitrobenzene 4- (N-phenethyl-N-benzyl-aminomethyl) -nitrobenzene 4- (N-phenethyl-N-cyclohexyl-aminomethyl) -nitrobenzene 4- (pyridin-2-yl) -ethyl) -N-methyl-aminomethyl] nitrobenzene 4- (pyridin-4-yl) -ethyl) -N-methyl-aminomethyl] nitrobenzene 4- (pyridin-4-yl-methyl) -N-methyl-aminomethyl] nitrobenzene 4- (dibenzylamino-methyl) -nitrobenzene 38 4- (4-nitro-benzyl) -N-propyl-aminomethyl] -nitrobenzene 4-[IN-benzyl-N- (3-cyano-propyl) -aminomethyl] -nitrobenzene 4- (N-benzyl-N-allyl-aminomethyl) -nitrobenzene 4- (benzo(1,3)dioxol-5-yl-methyl) -N-methyl-aminomethyl] nitrobenzene 4- (7-chloro-2,3,4,5-tetrahydro-benzo(d)azepin-3-ylmethyl) -nitrobenzene 4- (7,8-dichloro-2,3,4,5-tetrahydro-benzo(d)azepin-3-ylmethyl) -nitrobenzene 4- (7-methoxy-2,3,4,5-tetrahydro-benzo(d)azepin-3-ylmethyl) -nitrobenzene 4- (7-methyl-2,3,4,5-tetrahydro-benzo(d)azepin-3-ylmethyl) -nitrobenzene 4- (7,8-dimethoxy-2,3,4,5-tetrahydro-benzo(d)azepin-3-ylmethyl) -nitrobenzene 4-(6,7-dichloro-1,2,3,4-tetrahydro-isoquinolin-2-ylmethyl) -nitrobenzene 4-(6,7-dimethyl-1,2,3,4-tetrahydro-isoquinolin-2-ylmethyl) -nitrobenzene 4- (6-chloro-1,2,3,4-tetrahydro-isoquinolin-2-yl-methyl) nitrobenzene 4- (7-chloro-1,2,3,4-tetrahydro-isoquinolin-2-yl-methyl) nitrobenzene 39 4- (G-methoxy-l,2,3,4-tetrahydro-isoquinolin-2-yl-methyl) nitrobenzene 4- (7-methoxy-1,2,3,4-tetrahydro-isoquilolin-2-yl-methyl) nitrobenzene 4- (2,3,4,5-tetrahydro-azepino(4,5-b)pyrazil-3-yl) -methyl) nitrobenzene 4-(7-amino-2,3,4,5-tetrahydro-azepiflo(4,5-b)pyrazifl3-ylmethyl) -nitrobenzene 4-(2-amino-5,6,7,8-tetrahydro-azepiflo(4,5-d)thiazol-G-ylmethyl) -nitrobenzene 4-(5,G,7,8-tetrahydro-azepiflo(4,5-d)thiazol-G-yl-methyl)nitrobenzene Example VI 4- (N-Ethyl -N-tert .butoxycarbonvl-aminomethyl) -nitrobenzene 2.2 g of 4-(N-ethyl-aminomethyl)-litrobelzee are dissolved in 50 ml of ethyl acetate and stirred with 2.6 g of di-tert.butyl-dicarbonate for 30 minutes at ambient temperature. Then the solution is washed with water and concentrated by evaporation.

Yield: 3.4 g (97 11 of theory), Rf value: 0.90 (silica gel, methylene chloride/methanol 9:1) The following compounds are prepared analogously to Example VI: 4- (4-chlorophenylmethyl) -N-tert .butoxycarbonylaminomethyl] -nitrobenzene 40 4- (N-cyclohexyl-N-tert .butoxycarbonyl-aminomethyl) nitrobenzene 4- (N-isopropyl-N-tert .butoxycarbonyl-aminomethyl) nitrobenzene 4- (N-butyl-N-tert .butoxycarbonyl-aminomethyl) -nitrobenzene 4- (N-methoxycarbonylmethyl-N-tert.butoxycarbonylaminomethyl) -nitrobenzene 4- (N-benzyl-N-tert .butoxycarbonyl-aminomethyl) nitrobenzene 4- (N-ethyl-N-tert .butoxycarbonyl-aminomethyl) -nitrobenzene Example VII (N-Ethyl-N-tert .butoxvcarbonvl-aninomethvl) -aniline 6.4 g of 4- (N-ethyl-N-tert .butoxycarbonyl-aminomethyl) nitrobenzene are dissolved in 60 ml of methanol and hydrogenated with 1.5 g of Raney nickel at ambient temperature under 3 bar. The catalyst is then filtered off and the solution is evaporated down.

Yield: 4.78 g R. value: 0.70 (silica gel, methylene chloride/methanol 50:1) The following compounds are prepared analogously to Example VII: 4- (4-chlorophenylmethyl) -N-tert .butoxycarbonylaminomethyl) -aniline 4- (N-cyclohexyl-N-tert .butoxycarbonyl-aminomethyl) -aniline 41 4- (N-isopropyl-N-tert .butoxycarbonyl-aminomethyl) -aniline 4- (N-butyl-N-tert .butoxycarbonyl-aminomethyl) -aniline 4- (N-methaxycarbonylmethyl-N-tert.butoxycarbonylaminomethyl) -aniline 4- (N-benzyl-N-tert .butoxycarbonyl-aminomethyl) -aniline 4- (pyrrolidino-methyl) -aniline 4- (morpholino-methyl) -aniline 4- (piperidino-methyl) -aniline 4- (hexamethyleneimino-methyl) -aniline 4- (4-hydroxy-piperidino-methyl) -aniline 4- (4-methyl-piperidino-methyl) -aniline 4- (4-ethyl-piperidino-methyl) -aniline 4- (4-isopropyl-piperidino-methyl) -aniline 4- (4-phenyl -piperidino-methyl) -aniline 4- (4-benzyl-piperidino-methyl) -aniline 4- (4-ethoxycarbonyl-piperidino-methyl) -aniline 4- (dimethylarnino-methyl) -aniline 4- (di-n-propylamino-methyl) -aniline 4- (4-tert .butoxycarbonyl-piperazino-methyl) -aniline 42 3- (dimethylamino-methyl) -aniline 4- (2-diethylamino-ethyl) -aniline 4- (2-morpholino-ethyl) -aniline 4- (2-pyrrolidino-ethyl) -aniline 4- (2-piperidino-ethyl) -aniline 4- (N-ethyl-N-benzyl-aminomethyl) -aniline 4- (N-propyl-N-benzyl-aminomethyl) -aniline 4- (N-methyl-N- (4-chlorophenylmethyl) -aminomethyl) -aniline 4- (N-methyl-N- (4-bromophenylmethyl) -aminomethyl) -aniline 4- (N-methyl-N- (3-chlorophenylmethyl) -aminomethyl) -aniline 4- (N-methyl-N- (3,4-dimethoxyphenylmethyl) -aminomethyl) aniline 4- (N-methyl-N- (4-methoxyphenylmethyl) -aminomethyl) -aniline 4-EN- (2,2,2-trifluoroethyl) -N-benzyl-aminomethyl] -aniline 4-EN- (2,2,2-trifluoroethyl) (4-chlorophenylmethyl) aminomethyl] -aniline 4- 6-dimethyl-piperidino-methyl) -aniline 4- (thiomorpholino-methyl) -aniline 4- (S-oxido-thiomorpholino-methyl) -aniline 4- S-dioxido-thiomorpholino-methyl) -aniline 43 4- (azetidino-methyl) -aniline 4- (2,5-dihydropyrrol-l-yl-methyl) -aniline 4- (3,6-dihydro-2H-pyridin-l-yl-methyl) -aniline 4- (2-methoxycarbonyl-pyrrolidino-methyl) -aniline 4- (3,5-dimethyl-piperidino-methyl) -aniline 4- (4-phenyl-piperazino-methyl) -aniline 4- (4-phenyl-4-hydroxy-piperidino-methyl) -aniline 4- 5-trimethoxybenzyl )-N-methyl-aminomethyl] aniline 4- 4-dimethoxybenzyl) -N-ethyl-aminomethyl] -aniline 4- (N-benzyl-N-ethyl-aminomethyl) -aniline 4- (3-chilorobenzyl) -N-methyl-aminomethyl] -aniline 4- 6-dichlorobenzyl) -N-methyl-aminomethyl] -aniline 4- (4-trifluoromethylbenzyl) -N-methyl-aminomethyl) aniline 4- (N-benzyl-N-isopropyl-aminomethyl) -aniline 4- (N-benzyl-N-tert .butyl-aminomethyl) -aniline 4- (diisopropylamino-methyl) -aniline 4- (di-n-propylamino-methyl) -aniline 44 4- (diisobutylamino-methyl) -aniline 4- (2,3,4,5-tetrahydro-benzo(d)azepin-3-yl-methyl) -aniline 4- (2,3-dihydro-isoindol-2-yl-methyl) -aniline 4- (6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinolin-2-ylmethyl) -aniline 4- (1,2,3,4-tetrahydra-isoquinolin-2-yl-methyl) -aniline 4- (2-hydroxyethyl) -N-benzyl-aminomethyll -aniline 4-IN- (1-ethyl -pentyl) (pyridin-2-yl-methyl) aminomethyl] -aniline 4- (N-phenethyl-N-methyl-aminomethyl) -aniline 4-EN- (3,4-dihydroxy-phenethyl) -N-methyl-aminonethyl) aniline 4- 5-trimethoxy-phenethyl) -N-methyl-aminomethyl] aniline 4- 4-dimethoxy-phenethyl) -N-methyl-aminomethyl) aniline 4- (4-nitro-phenethyl) -N-methyl-aminomethyl) -aniline 4- (N-phenethyl-N-benzyl-aminomethyl) -aniline 4- (N-phenethyl-N-cyclohexyl-aminomethyl) -aniline 4- (pyridin-2-yl) -ethyl) -N-methyl-aminomethyl] aniline 45 4- (pyridin-4-yl) -ethyl) -N-methyl-aminomethyl] aniline 4- (pyridin-4-yl-methyl) -N-methyl-aminomethyl] -aniline 4- (dibenzylamino-methyl) -aniline 4- (4-nitro-benzyl) -N-propyl--aminomethyll -aniline 4- [N-benzyl-N- (3-cyano-propyl) -aminomethyl) -aniline 4- (N-benzyl-N-allyl-aminomethyl) -aniline 4- [N-benzyl-N- (2,2,2-trifluoroethyl) -aminomethyl] -aniline 4-EN- (benzo(1,3)dioxol-5-yl-methyl) -N-methyl-aminomethyl] aniline 4- (7-chloro-2,3,4,5-tetrahydro-benzo(d)azepin-3-ylmethyl) -aniline 4- (7,8-dichloro-2,3,4,5-tetrahydro-benzo(d)azepin-3-ylmethyl) -aniline 4- (7-methoxy-2,3,4,5-tetrahydro-benzo(d)azepin-3-ylmethyl) -aniline 4- (7-methyl-2,3,4,5-tetrahydro-benzo(d)azepin-3-ylmethyl) -aniline 4- (7,8-dimethoxy-2,3,4,5-tetrahydro-benzo(d)azepin-3-ylmethyl) -aniline 4-(6,7-dichloro-1,2,3,4-tetrahydro-isoquinolin-2-ylmethyl) -aniline -46 4-(6,7-dimethyl-1,2,3,4-tetrahydro--isoquinolin-2-ylmethyl) -aniline 4- (6-chloro-1,2,3,4-tetrahydro-isoquinolin-2-yl-methyl) aniline 4- (7-chloro-1,2,3,4-tetrahydro-isoquinolin-2-yl-methyl) aniline 4- (6-methoxy-1,2,3,4-tetrahydro-isoquinolin-2-yl-nethyl) aniline 4- (7-methoxy-1,2,3,4-tetrahydro-isoquinolin-2-yl-methyl) aniline 4-(2,3,4,5-tetrahydro-azepino(4,5-b)pyrazin-3-yl-methyl)aniline 4- (7-amino-2,3,4,5-tetrahydro-azepino(4,5-b)pyrazin-3-ylmethyl) -aniline 4-(2-amino-5,6,7,8-tetrahydro-azepino(4,5-d)thiazol-6-ylmethyl) -aniline 4-(5,6,7,8-tetrahydro-azepino(4,5-d)thiazol-6-yl-methyl)aniline 47 Preparation of the end products: Example 1 BIBE 1790 3-Z-(l-phenylamino-l-butyl-methylene)-5-amido-2-indolinone 600 g of a resin prepared according to Example IV were suspended in 3 ml of dimethylformamide and shaken with 0.4 g of aniline for 10 hours at 70 0 C. Then the mixture was filtered and the resin was washed several times with methylene chloride, methanol and dimethylformamide. Then 3 ml of methanolic ammonia were added for 2 hours in order to cleave the-acetyl group. Finally, after further washing with dimethylformamide and methylene chloride, 4 ml of trifluoroacetic acid in methylene chloride were added over 90 minutes, the resin was separated off and the solution was concentrated by evaporation. The residue was taken up in a little IN sodium hydroxide solution and extracted with a little methylene chloride. The organic phase was dried over sodium sulphate and concentrated by rotary evaporation.

Yield: 37 mg Rf value: 0.6 (silica gel, methylene chloride/methanol 9:1)

C

20

H

21

N

3 0 2 mass spectrum: m/z 335 The following compounds are prepared analogously to Example 1: 3-Z-(1-phenylamino-methylene)-5-amido-2-indolinone Prepared from the resin prepared according to Example IV(1) and aniline Rf value: 0.59 (silica gel, methylene chloride/methanol 9:1)

C

16

,H

3

N

3 0 2 mass spectrum: m/z 279 48 3-Z-[1-(4-methyl-phenylamino)-1-methyl-methylene]-5amido-2-indolinone Prepared from the resin according to Example IV(2) and 4methylaniline Rf value: 0.44 (silica gel, methylene chloride/methanol 9:1)

C

1

,H

17

N

3 0 2 mass spectrum: m/z 307 3-Z-[1-(4-Chloro-phenylamino)-1-methyl-methylene]-5amido-2-indolinone Prepared from-the resin according to Example IV(2) and 4chloroaniline Rf value: 0,45 (silica gel, methylene chloride/methanol 9:1)

C

1 ,Hl 4 C1N302 mass spectrum: m/z 327/329 3-Z-[1-(4-ethyl-phenylamino)-1-methyl-methylene]-5amido-2-indolinone Prepared from the resin according to Example IV(2) and 4ethylaniline Rf value: 0.43 (silica gel, methylene chloride/methanol 9:1)

C

19

H,

1

N

3 0 2 mass spectrum: m/z 321 3-Z-[1-(4-methoxy-phenylamino)-1-methyl-methylene]-5amido-2-indolinone Prepared from the resin according to Example IV(2) and 4methoxyaniline R, value: 0.46 (silica gel, methylene chloride/methanol 9:1)

C

1

H

1 7

,N

3

O,

mass spectrum: m/z 323 49 3-Z-[1-(4-iodo-phenylamino)-1-methyl-methylene]-5amido-2-indolinone Prepared from the resin according to Example IV(2) and 4iodoaniline Rf value: 0.36 (silica gel, methylene chloride/methanol 9:1)

C

17

HIIN

3 0 2 mass spectrum: m/z 419 3-Z-[1-(4-fluoro-phenylamino)-1-methyl-methylene]-5amido-2-indolinone Prepared from-the resin according to Example IV(2) and 4fluoroaniline Rf value: 0.60 (silica gel, methylene chloride/methanol 9:1)

C

1

,H,

4

FN

3 02 mass spectrum: m/z 311 3-Z-[1-(4-bromo-phenylamino)-1-methyl-methylene]-5amido-2-indolinone Prepared from the resin according to Example IV(2) and 4bromoaniline R, value: 0.53 (silica gel, methylene chloride/methanol 9:1)

C

17

H

14 BrN 3

O

2 mass spectrum: m/z 371/373 3-Z-(l-phenylamino-l-methyl-methylene)-5-amido-2indolinone Prepared from the resin according to Example IV(2) and aniline Rf value: 0,58 (silica gel, methylene chloride/methanol 9:1)

C

17 Hs 1

N

3 0 2 mass spectrum: m/z 293 (M 3-Z-(l-amino-l-methyl-methylene)-5-amido-2-indolinone 50 Prepared from the resin according to Example IV(2) and ammonia Rf value: 0,23 (silica gel, methylene chloride/methanol 9:1)

C

11

HIN

3 0 2 mass spectrum: m/z 217 (11) 3-Z-[1-(4-piperidinomethyl-phenylamino)-1-methylmethylene]-5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4-(piperidinomethyl)-aniline Rf value: 0,31- (silica gel, methylene chloride/methanol 9:1)

C

23

H

26 N402 mass spectrum: m/z 390 (12) 3-Z-[l-(4-pyrrolidinomethyl-phenylamino)-1-methylmethylene]-5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4pyrrolidinomethyl-aniline Rf value: 0.20 (silica gel, methylene chloride/methanol 4:1)

C

22

H

24

N

4 0 2 mass spectrum: m/z 376 (M (13) 3-Z-[1-(4-Dipropylaminomethyl-phenylamino)-1-methylmethylene]-5-amido-2-indolinone Prepared from the resin according to Example 11(2) and 4dipropylaminomethyl-aniline Rf value: 0.71 (silica gel, methylene chloride/methanol 4:1)

C

24 H3,N 4 0 2 mass spectrum: m/z 406 (14) 3-Z-[1-[4-(2-piperidinoethyl)-phenylamino]-1-methylmethylene]-5-amido-2-indolinone 51 Prepared from the resin according to Example IV(2) and 4- (2-piperidinoethyl)-aniline Rf value: 0.38 (silica gel, methylene chloride/methanol 4:1)

C

24

H

28

N

4 0 2 mass spectrum: m/z 404 (M 3-Z-[1-[4-(2-diethylaminoethyl)-phenylamino]-1-methylmethylene]-5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4- (2-diethylaminoethyl)-aniline Rf value: 0.33-(silica gel, methylene chloride/methanol 4:1)

C

23

H

2 BN402 mass spectrum: m/z 393 (M (16) 3-Z-[l-(4-Hexamethyleneiminomethyl-phenylamino)-1methyl-methylene]-5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4-hexamethyleneiminomethyl-aniline Rf value: 0.34 (silica gel, methylene chloride/methanol 4:1)

C

24

H

28 N40 2 mass spectrum: m/z 404 (17) 3-Z-[1-[4-(N-methyl-N-methansulphonyl-amino)phenylamino]-1-methyl-methylene]-5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4-(N-methyl-N-methanesulphonyl-amino)-aniline R, value: 0.36 (silica gel, methylene chloride/methanol 9:1)

C

19

H

20

N

4 0 4

S

mass spectrum: m/z 400 (18) 3-Z-[1-(4-methanesulphonylamino-phenylamino)-1-methylmethylene]-5-amido-2-indolinone 52 Prepared from the resin according to Example IV(2) and 4-methanesulphonylamino-aniline Rf value: 0.31(silica gel, methylene chloride/methanol 9:1)

C

18

HIN

4 0 4

S

mass spectrum: m/z 386 (19) 3-Z-[1-(4-Bromophenylamino)-1-ethyl-methylene]-5amido-2-indolinone Prepared from the resin according to Example IV(3) and 4-bromoaniline Rf value: 0.52- (silica gel, methylene chloride/methanol 9:1) C1,H 16 BrN 30 2 mass spectrum: m/z 385/387 (M /M+2 3-Z- [1-(4-piperidinomethyl-phenylamino)-1-ethylmethylene]-5-amido-2-indolinone Prepared from the resin according to Example IV(3) and 4-piperidinomethyl-aniline Rf value: 0.42 (silica gel, methylene chloride/methanol 4:1)

C

24 H28N402 mass spectrum: m/z 404 (M (21) 3-Z-[l-(4-piperidinomethyl-phenylamino)-1-propylmethylene]-5-amido-2-indolinone Prepared from the resin according to Example IV(4) and 4-piperidinomethyl-aniline Rf value: 0.49 (silica gel, methylene chloride/methanol 4:1)

C

25

H

30

N

4 0 2 mass spectrum: m/z 418 (22) 3-Z-[1-(4-Bromophenylamino)-1-propyl-methylene]-5amido-2-indolinone 53 Prepared from the resin according to Example IV(4) and 4-bromoaniline Rf value: 0,53 (silica gel, methylene chloride/methanol 9:1)

C,

19

H

1 BrN 30 2 mass spectrum: m/z 399/401 (23) 3-Z-[(4-Bromophenylamino)-methylene]-5-amido-2indolinone Prepared from the resin prepared according to Example IV(1) and 4-bromoaniline

C,,H

12 BrN30 2 mass spectrum: m/z 357/359 (24) 3-Z-[(4-piperidinomethyl-phenylamino)-methylene]-5amido-2-indolinone Prepared from the resin prepared according to Example IV(1) and 4-piperidinomethyl-aniline

C

22

H

24

N

4 0 2 mass spectrum: m/z 376 3-Z-[1-(4-Bromophenylamino)-1-butyl-methylene]-5amido-2-indolinone Prepared from the resin according to Example IV and 4-bromoaniline Rf value: 0,53 (silica gel, methylene chloride/methanol 9:1)

C

20

H

20 BrN 3 0 2 mass spectrum: m/z 413/415 (M (26) 3-Z-[1-(4-piperidinomethyl-phenylamino)-1-butylmethylene]-5-amido-2-indolinone Prepared from the resin according to Example IV and 4-piperidinomethyl-aniline R, value: 0.48 (silica gel, methylene chloride/methanol 4:1)

C

26

H

32

N

4 0, 54 mass spectrum: m/z 432 (27) 3-Z-Il-(4-piperidinomethyl-phenylamino)-1-ethenylmethylene]-5-amido-2-indolinone Prepared from the resin according to Example IV(5) and 4-piperidinomethyl-aniline (28) 3-Z-[1-(4-piperidinomethyl-phenylamino)-l-(3bromopropyl)-methylene]-5-amido-2-indolinone Prepared from the resin according to Example IV(6) and 4-piperidinomethyl-aniline (29) 3-Z-Il-(4-piperidinomethyl-phenylamino)-1-(2phenylsulphonylethyl)-methylene]-5-amido-2-indolinone Prepared from the resin according to Example IV(7) and 4-piperidinomethyl-aniline 3-Z-[1-[4-(2,6-dimethylpiperidinomethyl)-phenylamino]- 1-methyl-methylene]-5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4-(2,6-dimethylpiperidinomethyl)-aniline (31) 3-Z-[l-(4-Thiomorpholinomethyl-phenylamino)-1-methylmethylene]-5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4-thiomorpholinomethyl-aniline Rf value: 0.53 (silica gel, methylene chloride/methanol 9:1)

C

22

H

24

N

4 0 2

S

mass spectrum: m/z 408 (32) 3-Z-[l-[(4-Thiomorpholino-S-oxido-methyl)phenylamino]-1-methyl-methylene]-5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4- (thiomorpholino-S-oxido-methyl) -aniline Rf value: 0.21 (silica gel, methylene chloride/methanol 9:1) 55

C

22

H

24

N

4 03S mass spectrum: m/z 424 (33) 3-Z-[1-[4-(Thiomorpholino-S,S-dioxido-methyl)phenylamino]-1-methyl-methylene]-5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4-(thiomorpholino-S,S-dioxido-methyl)-aniline (34) 3-Z-[l-(4-Azetidionomethyl-phenylamino)-1-methylmethylenel -5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4-azetidionomethyl-aniline 3-Z-Il-[4-(2,5-Dihydropyrrol-l-yl-methyl)phenylaminol-i -methyl-methylene] -5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4-(2,5-dihydropyrrol-l-yl-methyl)-aniline Rf value: 0.10 (silica gel, methylene chloride/methanol 9:1)

C

22

H

22

N

4 0 2 mass spectrum: m/z 375 (36) 3-Z-[l-(4-(3,6-Dihydro-2H-pyridin-l-yl-methyl) phenylamino]-1-methyl-methylene]-5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4-(3,6-dihydro-2H-pyridin-l-yl-methyl)-aniline R, value: 0.20 (silica gel, methylene chloride/methanol 9:1)

C

23

H

24 40 2 mass spectrum: m/z 389 (37) 3-Z-[1-14-(2-ethoxycarbonyl-pyrrolidinomethyl)phenylamino]-1-methyl-methylene]-5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4- (2-ethoxycarbonyl-pyrrolidinomethyl) -aniline Rf value: 0.50 (silica gel, methylene chloride/methanol 9:1) 56

C

2 4

H

2 6

N

4 04 mass spectrum: m/z 435 (MH)' (38) 3-Z-[l-[4-(3,5-dimethyl-piperidinomethyl)phenylamino]-1-methyl-methylene] -5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4-(3,5-dimethyl-piperidinomethyl)-aniline Rf value: 0.16 (silica gel, methylene chloride/methanol 9:1)

C

25

H

30

N

4 0 2 mass spectrum: m/z 418 (39) 3-Z-[1-[4-(4-phenyl-piperazinylmethyl)-phenylamino]- 1-methyl-methylene]-5-amido-2-indolinone-trifluoroacetate Prepared from the resin according to Example IV(2) and 4-(4-phenyl-piperazinylmethyl)-aniline Rf value: 0.40 (silica gel, methylene chloride/methanol 9:1)

C

28

H

29

N

5 0 2 mass spectrum: m/z 468 3-Z-[1-[4-(4-phenyl-4-hydroxy-piperidinylmethyl)phenylamino]-l-methyl-methylene]-5-amido-2-indolinonetrifluoroacetate Prepared from the resin according to Example IV(2) and 4-(4-phenyl-4-hydroxy-piperidinylmethyl)-aniline

C

29

H

30

N

4 0 3 mass spectrum: m/z 483 (41) 3-Z- (3-methoxy-phenylamino) amido-2-indolinone Prepared from the resin according to Example IV(2) and 3-methoxy-aniline Rf value: 0.40 (silica gel, methylene chloride/methanol 9:1)

C

18

H

17

N

3 0 3 Mass spectrum: m/z 323 57 (42) 3-Z-[l-(3-ethoxycarbonyl-phenylamino)-1-methylmethylene]-5-amido-2-indolinone Prepared from the resin according to Example IV(2) and ethyl 3-amino-benzoate

C

20

H

19 30 4 Mass spectrum: m/z 365 (43) 3-Z-[l-(4-dimethylaminomethyl-phenylamino)-1methylmethylen]-5-amido-2-indolinone trifluoroacetate Prepared from the resin according to Example IV(2) and 4-dimethylaminomethyl-aniline

C

20

H

22

N

4 0 2 Mass spectrum: m/z 351 (44) 3-Z- (4-Cyclohexyl-piperidinylmethyl) phenylamino]-1-methyl-methylene]-5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4-(4-cyclohexyl-piperidinylmethyl)-aniline (45) 3-Z- (4-morpholinyl-phenylamino) -1-methylmethylene]-5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4-morpholinyl-aniline

C

21

H

22 40 3 Mass spectrum: m/z 378 (46) 3-Z-[l-(N-methyl-piperidin-4-ylamino)-1-methylmethylene)-5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4-amino-N-methyl-piperidine

C

17

H

22

N

4 0 2 Mass spectrum: m/z 314 (47) 3-Z-[l-(4-methylcyclohexylamino)-1-methyl-methylene]- 5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4-methyl-cyclohexylamine 58

C

18

H

23

N

3 0 2 Mass spectrum: m/z 313 (48) 3-Z- (l-Cyclopentylamino,-l-methyl-methylene) 2-indolinone Prepared from the resin according to Example IV(2) and cyclopentylamine Rf value: 0. 70 (silica gel, methylene chloride /methanol 4:1)

C

16

H

19

N

3 0 2 Mass spectrum: m/z 285 (Mi) (49) 3-Z- (1-isopropylamino-1-methyl-methylene) 2 -indolinone Prepared from the resin according to Example IV(2) and isopropylamine

C

1 4 1 7 3 2 Mass spectrum: m/z 259 (50) 3-Z- [1-(4-ethoxycarbonylmethylaminomethylphenylamino) -1-methyl-methylene] -5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4- (ethoxycarbonylmethyl-N-tert .butyloxycarbonylaminomethyl) -aniline

C

21

H

22

N

4 0 4 Mass spectrum: m/z 394 (51) 3-Z- El- (4-benzylaminomethyl-phenylamino) -1-methylmethylene] -5-amido-2-indolinone Prepared from the resin according to Example IV(2) and 4- (N-benzyl-N-tert .butyloxycarbonyl-aminomethyl) -aniline Rf value: 0.24 (silica gel, methylene chloride/methanol= 9:1)

C

2

SH

24

N

4 0 2 Mass spectrum: m/z 412 59 (52) 3-Z-[l-(4-Butylaminomethyl-phenylamino)-1-methylmethylene]-5-amido-2-indolinone trifluoroacetate Prepared from the resin according to Example IV(2) and 4-(N-butyl-N-tert.butyloxycarbonyl-aminomethyl)-aniline Rf value: 0.40 (silica gel, methylene chloride/methanol 4:1)

C

22

H

26

N

4 0 2 Mass spectrum: m/z 378 (53) 3-Z- Ill- (4-ethylaminomethyl-phenylamino) -1-methylmethylene]-5-amido-2-indolinone trifluoroacetate Prepared from'the resin according to Example IV(2) and 4-(N-ethyl-N-tert.butyloxycarbonyl-aminomethyl)-aniline Rf value: 0.20 (silica gel, methylene chloride/methanol 4:1)

C

20

H

22

N

4 0 2 Mass spectrum: m/z 351 (54) 3-Z-[l-(4-Cyclohexylaminomethyl-phenylamino)-1-methylmethylene] -5-amido-2-indolinone trifluoroacetate Prepared from the resin according to Example IV(2) and 4-(cyclohexyl-(N-tert.butyloxycarbonyl-amino-methyl)aniline

C

24

H

28

N

4 0 2 Mass spectrum: m/z 405 3-Z-[l-(4-isopropylaminomethyl-phenylamino)-1-methylmethylene]-5-amido-2-indolinone trifluoroacetate Prepared from the resin according to Example IV(2) and 4-(N-isopropyl-N-tert .butyloxycarbonyl-aminomethyl)-aniline

C

21

H

24

N

4 0 2 Mass spectrum: m/z 365 (56) 3-Z-(l-(4-trifluoromethoxy-phenylamino)-i-methylmethylene -5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and 4trifluoromethoxy-aniline

C

18

H

14

F

3

N

3 0 3 mass spectrum: m/z 377 (57) 3-Z- [1-(4-difluoromethoxy-phenylamino) -1-methylmethylene] -5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and 4di fluoromethoxy- aniline Rf value: 0.5 (silica gel, methylene chloride/methanol 9:1)

C

18

H

15

F

2

N

3 0 3 mass spectrum: m/z 359 (58) 3-Z- [1-(4-bromo-3-chloro-phenylamino) -1-methylmethylene] -5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and 4bromo-3 -chioro-aniline

C

17

H

13 BrC1N 3 0 2 mass spectrum: m/z 405/407/409 (59) 3-Z-[Il- (4-trifluoromethyl-3-bromo-phenylamino) -1methyl-methylene] -5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and 4trifluoromethyl-3 -bromo-aniline

C

1

,H

13 BrF 3

N

3 02 mass spectrum: m/z 439/441 3-Z- [1-(4-chioro-phenylamino) -methylene] -5-amido-2indolinone Prepared from the resin produced in Example IV(l) and 4chloro-aniline

C

1 6

GH

12 C1N 3 0 2 mass spectrum: m/z 312/314 (61) 3-Z- [1-(3-bromo-phenylamino) -1-iethyl-methylene] amido-2-indolinone Prepared from the resin produced in Example IV(2) and 3bromo-aniline 61

C

17

H,

4 BrN 30 2 mass spectrum: m/z 371/373 (M (62) 3-Z-[1-(3-chloro-phenylamino)-1-methyl-methylene]-5amido-2-indolinone Prepared from the resin produced in Example IV(2) and 3chloro-aniline

C

17

H

14 C1N 3 0 2 mass spectrum: m/z 327/329 (M (63) 3-Z-[l-(2-chloro-phenylamino)-1-methyl-methylene]-5amido-2-indolinone Prepared from the resin produced in Example IV(2) and 2chloro-aniline

C

1

,H,

4

CN

3 0 2

O

mass spectrum: m/z 327/329 (M (64) 3-Z-[1-(4-bromo-3-methyl-phenylamino)-1-methylmethylene]-5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and 4bromo-3-methyl-aniline Rf value: 0.60 (silica gel, methylene chloride/methanol 9:1

C,

8 H1,BrN 3

O

2 mass spectrum: m/z 385/387 (M+ 3-Z-[1-(4-bromo-3-methoxy-phenylamino)-1-methylmethylene]-5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and 4bromo-3-methoxy-aniline Rf value: 0.60 (silica gel, methylene chloride/methanol 9:1

C

18

H

16 BrN 3

O

3 mass spectrum: m/z 401/403 (66) 3-Z-[1-(4-fluoro-3-nitro-phenylamino)-1-methylmethylene]-5-amido-2-indolinone 62 Prepared from the resin produced in Example IV(2) and 4fluoro-3-nitro-aniline Rf value: 0.40 (silica gel, methylene chloride/methanol 9:1

C

17

H

13

FN

4 0 4 mass spectrum: m/z 356 (67) 3-Z-[1-(4-bromo-3-nitro-phenylamino)-1-methylmethylene]-5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and 4bromo-3-nitro-aniline Rf value: 0.50' (silica gel, methylene chloride/methanol 9:1

C

1

,H

13 BrN 4 0 4 mass spectrum: m/z 416/418 (M (68) 3-Z-[1-(4-Ethyl-3-nitro-phenylamino)-1-methylmethylene]-5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and 4ethyl-3-nitro-aniline Rf value: 0.70 (silica gel, methylene chloride/methanol 9:1

C

19 HIsN 4 0 4 mass spectrum: m/z 366 (69) 3-Z-[1-(4-chloro-3-nitro-phenylamino)-1-methylmethylene]-5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and 4chloro-3-nitro-aniline

C

1

,H,

3 C1N 4 0 4 mass spectrum: m/z 371/373 (M 3-Z-[l-(3-Nitro-phenylamino)-1-methyl-methylene]-5amido-2 -indolinone Prepared from the resin produced in Example IV(2) and 3nitro-aniline

C

17

HI

4

N

4 04 63 mass spectrum: m/z 338 (71) 3-Z-[1-(4-Methyl-3-nitro-phenylamino)-1-methylmethylene]-5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and 4methyl-3-nitro-aniline Rf value: 0.50 (silica gel, methylene chloride/methanol 9:1

C

18

H

16

N

4 0 4 mass spectrum: m/z 352 (72) 3-Z-[1-(4-bromo-3-methoxycarbonyl-phenylamino)-1methyl-methylene]-5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and methyl Rf value: 0.50 (silica gel, methylene chloride/methanol 9:1 C1 9 H16BrN30 4 mass spectrum: m/z 429/431 (73) 3-Z-[l-(4-Carbamoyl-phenylamino)-1-methyl-methylene- 5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and 4aminobenzamide Rf value: 0,20 (silica gel, methylene chloride/methanol 9:1

C,

1 6HiN 4 0 3 mass spectrum: m/z 336 (74) 3-Z-[1-(4-(Piperidino-carbonyl)-phenylamino)-lmethyl-methylene]-5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and 1- (4-amino-benzoyl)-piperidine Rf value: 0.50 (silica gel, methylene chloride/methanol 9:1

C

2

,H

24

N

4 0 3 mass spectrum: m/z 404 64 3-Z-[1-(4-(2-(diethylamino)-ethyl-carbamoyl)phenylamino)-l-methyl-methylene]-5-amido-2-indolinonetrifluoracetate Prepared from the resin produced in Example IV(2) and 4amino-N-[2-(diethylamino)-ethyl]-benzamide Rf value: 0.30 (silica gel, methylene chloride/methanol 9:1 C 4

H

29 mass spectrum: m/z 436 (M+H (76) 3-Z-[l-(4-trifluoromethyl-phenylamino)-1-methylmethylene]-5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and 4trifluoromethyl-aniline

C

1 8

H

14

F

3

N

3 0 2 mass spectrum: m/z 361 (77) 3-Z-[l-(3-Hydroxymethyl-phenylamino)-1-methylmethylene]-5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and 3aminobenzylalcohol

C

1 8 17 3 03 mass spectrum: m/z 323 (78) 3-Z-[l-(4-(Hydroxycarbonyl-phenylamino)-1-methylmethylene]-5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and 4aminobenzoic acid R. value: 0.20 (silica gel, methylene chloride/methanol 4:1

C

18

H

15 30 4 mass spectrum: m/z 336 (79) 3-Z- (4-Ethoxycarbonylmethyl-3-nitro-phenylamino) 1-methyl-methylene]-5-amido-2-indolinone 65 Prepared from the resin produced in Example IV(2) and ethyl 4-amino-2-nitro-phenylacetate Rf value: 0.70 (silica gel, methylene chloride/methanol 9:1

C

21

H

20

N

4 0, mass spectrum: m/z 424 3-Z-[l-(3-Methoxycarbonyl-4-methyl-phenylamino)-1methyl-methylene]-5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and methyl 3-amino-6-methyl-benzoate Rf value: 0.70' (silica gel, methylene chloride/methanol 9:1

C

20 HIN3O4 mass spectrum: m/z 365 (81) 3-Z-[1-(3-Diethylcarbamoyl-4-methyl-phenylamino)-1methyl-methylene]-5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and 3amino-6-methyl-benzoic acid diethylamide R, value: 0.50 (silica gel, methylene chloride/methanol 9:1

C

23

H

2 6N403 mass spectrum: m/z 406 (82) 3-Z-[1-(3-Ethylcarbamoyl-4-methyl-phenylamino)-1methyl-methylene]-5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and 3amino-6-methyl-benzoic acid ethylamide Rf value: 0.40 (silica gel, methylene chloride/methanol 9:1)

C

21

H

22

N

4 0 3 mass spectrum: m/z 378 (83) 3-Z-[1-(3-Sulphamoyl-4-methyl-phenylamino)-1-methylmethylene]-5-amido-2-indolinone 66 Prepared from the resin produced in Example IV(2) and 3amino-6-methyl-phenylsulphonic acid amide Rf value: 0.30 (silica gel, methylene chloride/methanol 9:1)

C

18

H

18

N

4 0 4

S

mass spectrum: m/z 386 (84) 3-Z-[l-(3-Acetylamino-4-methyl-phenylamino)-1-methylmethylene]-5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and 4amino-2-acetylamino-toluene R, value: 0.65 (silica gel, methylene chloride/methanol 9:1)

C

20

H

2 oN 4 0 3 mass spectrum: m/z 364 3-Z-[1-(4-(2-Dimethylamino-ethoxy)-phenylamino)-1methyl-methylene]-5-amido-2-indolinone-trifluoroacetate Prepared from the resin produced in Example IV(2) and 4- (2-dimethylamino-ethoxy)-aniline Rf value: 0,10 (silica gel, methylene chloride/methanol 4:1

C

21 H,4N403 mass spectrum: m/z 380 (86) 3-Z-[l-(4-(2-Piperidino-ethoxy)-phenylamino)-lmethyl-methylene]-5-amido-2-indolinone-trifluoroacetate Prepared from the resin produced in Example IV(2) and 4- (2-piperidino-ethoxy)-aniline Rf value: 0.70 (silica gel, methylene chloride/methanol 4:1

C

24

H

28 N403 mass spectrum: m/z 420 (87) 3-Z-[1-(4-(3-Dimethylamino-propoxy)-phenylamino)-1methyl-methylene]-5-amido-2-indolinone-trifluoroacetate 67 Prepared from the resin produced in Example IV(2) and 4- (3-dimethylamino-propoxy)-aniline R, value: 0.10 (silica gel, methylene chloride/methanol 4:1

C

22

H

26

N

4 0 3 mass spectrum: m/z 394 (88) 3-Z-[1-(4-(3-Piperidino-propoxy)-phenylamino)-1methyl-methylene]-5-amido-2-indolinone-trifluoroacetate Prepared from the resin produced in Example IV(2) and 4- (3-piperidino-propoxy)-aniline Rf value: 0.20' (silica gel, methylene chloride/methanol 4:1

C

25

H

30 N403 mass spectrum: m/z 434 (89) 3-Z-[1-(4-(3-(N-Benzyl-N-methylamino)-propoxy)phenylamino)-1-methyl-methylene]-5-amido-2-indolinonetrifluoroacetate Prepared from the resin produced in Example IV(2) and 4- [3-(N-benzyl-N-methylamino)-propoxy]-aniline Rf value: 0.60 (silica gel, methylene chloride/methanol 4:1

C

28

H

3 0N4 03 mass spectrum: m/z 470 3-Z-[1-(4-(N-benzyl-aminomethyl)-phenylamino)methylene]-5-amido-2-indolinone-trifluoroacetate Prepared from the resin produced in Example IV(1) and 4- (N-benzyl-N-tert.butoxcarbonyl-aminomethyl)-aniline

C

24

H

22

N

4 0 2 mass spectrum: m/z 399 (91) 3-Z-[l-(4-(N-(4-chlorobenzyl)-aminomethyl)phenylamino)-1-methyl-methylene]-5-amido-2-indolinonetrifluoroacetate Prepared from the resin produced in Example IV(2) and 4- 68 [N-(4-chlorobenzyl-N-tert.butoxycarbonyl-aminomethyl)aniline Rf value: 0.40 (silica gel, methylene chloride/methanol 9:1)

C

25

H

23 C1N 4 0 2 mass spectrum: m/z 446/448 (92) 3-Z-[1-(4-(N-(3,4,5-Trimethoxybenzyl)-N-methylaminomethyl)-phenylamino)-1-methyl-methylene]-5-amido-2indolinone-trifluoroacetate Prepared from the resin produced in Example IV(2) and 4- [N-((3,4,5-trimethoxy-benzyl)-N-methyl-aminomethyl]aniline Rf value: 0.50 (silica gel, methylene chloride/methanol 9:1)

C

29

H

32

N

4 0 mass spectrum: m/z 516 (93) 3-Z-[1-(4-(N-(3,4-Dimethoxy-benzyl)-N-methyl-aminomethyl) -phenylamino) -1-methyl -methylene] -5-amido-2indolinone-trifluoroacetate Prepared from the resin produced in Example IV(2) and 4- [N-(3,4-dimethoxy-benzyl)-N-methyl-aminomethyl]-aniline Rf value: 0.40 (silica gel, methylene chloride/methanol 9:1)

C

28

H

30

N

4 0 4 mass spectrum: m/z 486 (94) 3-Z-[l-(4-(N-(3,4-Dimethoxy-benzyl)-N-ethylaminomethyl) -phenylamino) -1-methyl-methylene -5-amido-2indolinone-trifluoroacetate Prepared from the resin produced in Example IV(2) and 4- [N-(3,4-dimethoxy-benzyl)-N-ethyl-aminomethyl]-aniline R, value: 0.40 (silica gel, methylene chloride/methanol 9:1)

C

29

H

32 4 04 mass spectrum: m/z 500 (MI) 69 3-Z-[li- (N-Benzyl-N-ethyl-aminomethyl) phenylamino) -1-methyl-methylene] -5-amido-2-indolinonetrifluoroacetate Prepared from the resin produced in Example IV(2) and 4- (N-benzyl-N-ethyl-aminomethyl) -aniline Rf value: 0.50 (silica gel, methylene chloride/methanol 9:1)

C

2 7

H

2 8 4 2 mass spectrum: m/z 440 (96) 3-Z- (N-Benzyl-N-methyl-aminomethyl) phenylamino) -1-methyl-methylene] -5-amido-2-indolinonetrifluoroacetate Prepared from the resin produced in Example IV(2) and 4- (N-benzyl-N-methyl-aminomethyl) -aniline Rf value: 0,55 (silica gel, methylene chloride/methanol 9:1)

C

26

H

26

N

4 0 2 mass spectrum: m/z 426 (97) 3-Z- Il- (N-Benzyl-N-methyl-aminomethyl) phenylamino) -1-ethyl-methylene] -5-amido-2-indolinonetrifluoroacetate Prepared from the resin produced according to Example IV(3) and 4- (N-benzyl-N-methyl-aminomethyl) -aniline R. value: 0.50 (silica gel, methylene chloride/methanol= 9:1)

C

27

H-

28

N

4 0 2 mass spectrum: m/z 440 (98) 3-Z-[li- (N-Benzyl-N-methyl-aminomethyl) phenylamino) -1-propyl-methylene] -5-amido-2-indolinonetrifluoroacetate Prepared from the resin produced according to Example IV(4) and 4- (N-benzyl-N-methyl-amino-methyl) -aniline Rf value: 0. 50 (silica gel, methylene chloride /methanol 9:1)

C

28

H

3

N

0 2 mass spectrum: m/z 454 (99) 3-Z- (4-chlorobenzyl) -N-methyl-aminomethyl) phenylamino) -1-methyl-methylene] -5-amido-2-indolinonetrifluoroacetate Prepared from the resin produced in Example IV(2) and 4- (4-chlorobenzyl) -N-methyl-aminomethyl] -aniline Rf value: 0.40 (silica gel, methylene chloride/methanol 9:1)

C

2 6H 25 C1N 4 02 mass spectrum: m/z 460/462 (100) 3-Z- (3-chlorobenzyl) -N-methyl-aminomethyl) phenylamino) -1-methyl-methylene] -5-amido-2-indolinonetrifluoroacetate Prepared from the resin produced in Example IV(2) and 4- (3-chlorobenzyl) -N-methyl-aminomethyl] -aniline Rf value: 0.40 (silica gel, methylene chloride /methanol= 9:1)

C

26

H

25 C1N 4 02 mass spectrum: m/z 460/462 (101) 3-Z-[l-(4-(N-(2,6-dichlorobenzyl)-N-methylaminomethyl) -phenylamino) -1-methyl-methylene] -5-amido-2indolinone-trifluoroacetate.

Prepared from the resin produced in Example IV(2) and 4- 6-dichlorobenzyl) -N-methyl-aminomethyl] -aniline Rf value: 0,38 (silica gel, methylene chloride/methanol= 9:1)

C

26

H

24 C1 2

N

4 0 2 mass spectrum: m/z 494/496/498 (102) 3-Z- (4-trifluoromethylbenzyl) -N-methylaminomethyl) -phenylamino) -1-methyl-methylene] -5-amido-2- 71 indol inone- trifluoroacetate Prepared from the resin produced in Example IV(2) and 4- (4-trifluoromethylbenzyl) -N-methyl-aminomethyl] -aniline Rf value: 0,38 (silica gel, methylene chloride/methanol 9:1)

C

27

H

25

F

3

N

4 0 2 mass spectrum: m/z 494 WM) (103) 3-Z- (N-Benzyl-N-isopropyl-aminomethyl) phenylamino) -1-methyl-methylene] -5-amido-2-indolinonetrifluoroacetate Prepared from-~the resin produced in Example IV(2) and 4- (N-benzyl-N-isopropyl-aminomethyl) -aniline Rf value: 0.50 (silica gel, methylene chloride/methanol 9:1)

C

28

H

3

N

02 mass spectrum: m/z 454 (104) (N-benzyl-N-tert.butyl-aminomethyl) phenylamino) -1-methyl-methylene] -5-amido-2-indolinonetrifluoroacetate Prepared from the resin produced in Example IV(2) and 4- (N-benzyl-N-tert .butyl-aininomethyl) -aniline Rf value: 0.50 (silica gel, methylene chloride/methanol= 9:1)

C

29

H

32

N

4 0 2 mass spectrum: m/z 468 (105) 3-Z- (N-benzyl-N-methyl-aminomethyl) phenylamino) -methylene] -5-amido-2-indolinonetrifluoroacetate Prepared from the resin produced in Example IV(1) and 4- (N-benzyl-N-methyl-aminomethyl) -aniline

C

25

H

24

N

4 02 mass spectrum: m/z 413 72 (106) 3-Z-(l-(4-(N-benzyl-N-ethyl-aminomethyl)phenylamino) -1-methyl-methylene] -5-amido-2-indolinonetrifluoroacetate Prepared from the resin produced in Example IV(1) and 4- (N-benzyl-N-ethyl-aminomethyl) -aniline

C

26 26 4 2 mass spectrum: m/z 427 (M+H 4 (107) 3-Z- (Diisopropylamino-methyl) -phenylamino) 1-methyl-methylene] -5-amido-2-indolinone-trifluoroacetate Prepared from the resin produced in Example IV(2) and 4- (diisopropylam-fino-methyl) -aniline Rf value: 0.50 (silica gel, methylene chloride/methanol 4:1)

C

24

H

3

N

02 mass spectrum: m/z 406 (108) 3-Z- (Di-n-propylamino-methyl) -phenylamino) methylene] -5-amido-2-indolinone-trifluoroacetate Prepared from the resin produced in Example IV(2) and 4- (di-n-propylamino-methyl) -aniline

C

23

H

28

N

4 0 2 mass spectrum: m/z 393'(M+ H+) (109) 3-Z- (diisobutylamino-methyl) -phenylamino) 1-methyl-methylene] -5-amido-2-indolinone-trifluoroacetate Prepared from the resin produced in Example IV(2) and 4- (diisobutylamino-methyl) -aniline Rf value: 0.50 (silica gel, methylene chloride/methanol 9:1)

C

2 6

H-

34

N

4 0 2 mass spectrum: m/z 434 (110) 3-Z-[1-(4-(2,3,4,5-Tetrahydro-benzo(d)azepin-3-ylmethyl) -phenylamino) -1-methyl -methylene] -5-amido-2indol inone-trifluoroacetate

C,

73 Prepared from the resin produced in Example IV(2) and 4- (2,3,4,5-tetrahydro-benzo(d)azepin-3-yl-methyl) -aniline Rf value: 0.30 (silica gel, methylene chloride/methanol 9:1)

C

28 11 28

N

4 0 2 mass spectrum: m/z 452 (111) 3-Z-[1-(4-(l,3-Dihydro-isoindol-2-yl-methyl)phenylamino) -1-methyl-methylenel -5-amido-2-indolinonetrifluoroacetate Prepared from the resin produced in Example IV(2) and 4- (1,3-dihydro-isoindol-2-yl-methyl) -aniline Rf value: 0,35 (silica gel, methylene chloride/methanol= 9:1)

C

26

H

24

N

4 0 2 mass spectrum: m/z 425 (112) 3-Z-[1-(4-(6,7-Dimethoxy-l,2,3,4-tetrahydroisoquinolin-2-yl-methyl) -phenylamino) -1-methyl-methylene] 5-amido-2-indolinone-trifluoroacetate Prepared from the resin produced in Example IV(2) and 4- 7-dimethoxy-1, 2,3, 4-tetrahydro-isoquinolin-2-ylmethyl) -aniline Rf value: 0.50 (silica gel, methylene chloride/methanol 9:1)

C

29

H-

30

N

4 0 4 mass spectrum: m/z 499 (113) 3-Z-[l-(4-(1,2,3,4-tetrahydro-isoquinolin-2-ylmethyl) -phenylamino) -1-methyl-methylene] -5-amido-2indolinone -trifluoroacetate Prepared from the resin produced in Example IV(2) and 4- (1,2,3,4-tetrahydro-isoquinolin-2-yl-methyl) -aniline 74 (114) 3-Z-[l-(4-(N-(Ethoxycarbonylmethyl)-N-benzylaminomethyl)-phenylamino)-1-methyl-methylene]-5-amido-2indolinone-trifluoroacetate Prepared from the resin produced in Example IV(2) and 4- [N-(ethoxycarbonylmethyl)-N-benzyl-aminomethyl)-aniline Rf value: 0.60 (silica gel, methylene chloride/methanol 9:1)

C

29

H

3 ON4 0 4 mass spectrum: m/z 498 (115) 3-Z-[1-(4-(N-(2-Hydroxyethyl)-N-benzyl-aminomethyl)phenylamino)-1-methyl-methylene]-5-amido-2-indolinonetrifluoroacetate Prepared from the resin produced in Example IV(2) and 4- [N-(2-hydroxyethyl)-N-benzyl-aminomethyl)-aniline R. value: 0.40 (silica gel, methylene chloride/methanol 9:1)

C

27

H

28 40 3 mass spectrum: m/z 456 (116) 3-Z-[1-(4-(N-(-Ethyl-pentyl)-N-(pyridin2yl methyl) amido-2-indolinone-trifluoroacetate Prepared from the resin produced in Example IV(2) and 4- [N-(l-ethyl-pentyl)-N-(pyridin-2-yl-methyl)-aminomethyl]aniline Rf value: 0,45 (silica gel, methylene chloride/methanol 9:1)

C

31 1 37

N

5 0 2 mass spectrum: m/z 511 (117) 3-Z-[l-(4-(Piperidino-methyl)-3-nitro-phenylamino)- 1-methyl-methylene]-5-amido-2-indolinone Prepared from the resin produced in Example IV(2) and 4- (piperidino-methyl)-3-nitro-aniline Rf value: 0.70 (silica gel, methylene chloride/methanol 9:1)

C

23

H

25

N

5 0 4 mass spectrum: m/z 436 (118) 3-Z- (N-Phenethyl-N-methyl-aminomethyl) phenylamino) -1-methyl-methylene] -5-amido-2-indolinonetrifluoroacetate Prepared from the resin produced in Example IV(2) and 4- (N-phenethyl-N-methyl-aminomethyl) -aniline Rf value: 0.50o (silica gel, methylene chloride /methanol 9:1)

C

27

H

28

N

4 0 2 mass spectrum:' m/z 441 (119) 3-Z-[Il- (N-phenethyl-N-ethyl-aminomethyl) phenylamino) -1-methyl-methylene] -5-amido-2-indolinone (120) 3-Z- (3,4-dihydroxy-phenethyl) -N-methylamino-methyl) -phenylamino) -1-methyl-methylene] -5-amido-2indol inone (121) 3-Z-[1-(4-(N-(3,4,5-trimethoxy-phenethyl)-N-methylaminomethyl) -phenylamino) -1-methyl-methylene] 2 -indolinone (122) 3-Z-[1-(4-(N-(3,4-dimethoxy-phenethyl)-N-methylamino-methyl) -phenylamino) -1-methyl-methylene] -5-amido-2indolinone (123) 3-Z-[l-(4-(N-(4-nitro-phenethyl)-N-methylaminomethyl) -phenylamino) -1-methyl-methylene] -5-amido-2indol inone (124) 3-Z- (N-phenethyl-N-benzyl-aminomethyl) phenylamino) -l-methyl-methylene] -5-amido-2-indolinone 76 (125) 3-Z- (N-phenethyl-N--cyclohexyl-aminomethyl) phenylamino) -1-methyl-methylene] -5-amido-2-indolinone (126) 3-Z-[1-(4-(N-(4-nitro-phenethyl)-N-isopropylaminomethyl) -phenylamino) -1-methyl-methylene] -5-arnido-2indol inane (127) 3-Z-[1-(4-(N-(2-(pyridin-2-yl)-ethyl)-N-methylamino-methyl) -phenylamino) -1-methyl-methylene] -5-amido-2indolinone (128) 3-Z-[1-(4-(N-(2-(pyridin-4-yl)-ethyl)-N-methylamino-methyl) -phenylamino) -1-methyl-methylene] -5-amido-2indol inane (129) 3-Z- (pyridin-2-yl-methyl) -N-methyl-aminomethyl) -phenylamino) -1-methyl-methylenel -5-amido-2indol inane (130) 3 (4 (pyridin-3 -y1-methyl)--N-methyl -aminomethyl) -phenylamino) -1-methyl-methylene] -5-amido-2indol inane (131) 3 (pyridin-4-yl-methyl) -N-methyl -aminomethyl) -phenylamino) -1-methyl-methylene] -5-amido-2indol inane (132) 3-Z- (dibenzylamino-methyl) -phenylamino) -1methyl-methylene] -5-amido-2-indolinone (133) 3-Z- (4-nitro-benzyl) -N-propyl-aminomethyl) phenylamino) -1-methyl-methylene] -5-amido-2-indalinone (134) 3-Z- (N-benzyl-N- (3-cyano-propyl) -aminomethyl) phenylamino) -1-methyl -methylene] -5-amido-2-indalinone 77 (135) 3-Z-[1-(4-(N-benzyl-N-allyl-aminomethyl)phenylamino) -1-methyl-methylene] -5-amido-2-indolinone (136) 3-Z-[l-(4-(imidazol-1-yl-methyl)-phenylamino)-1methyl-methylene] -5-amido-2-indolinone (137) 3-Z- (imidazol-2-yl-amino-methyl) -phenylamino) 1-methyl-methylene] -5-amido-2-indolinone (138) 3-Z-[1-(4-(N--benzyl-N-(2,2,2-trifluoroethyl)aminomethyl) -phenylamino) -1-methyl-methylene] -5-amido-2indolinone (139) 3-Z-[l-(4-(N-(benzo(1,3)dioxol-5-yl-methyl)--Nmethyl-aminomethyl) -phenylamino) -1-methyl -methylene] amido -2-indol inone (140) 3-Z-[l-(4-(7-chloro-2,3,4,5-tetrahydrobenzo azepin-3-yl-methyl) -phenylamino) -1-methylmethylene] -5-amido-2-indolinone (141) 3-Z-[1-(4-(7,8-dichloro-2,3,4,5-tetrahydrobenzo(d)azepin-3-yl-methyl) -phenylamino) -1-methylmethylene] -5-amido-2-indolinone (142) 3-Z-[1-(4-(7-bromo-2,3,4,5-tetrahydrobenzo(d)azepin-3-yl-methyl) -phenylamino) -1-methylmethylene] -5-amido-2-indolinone (143) 3-Z-[1-(4-(7-fluoro-2,3,4,5-tetrahydrobenzo(d)azepin-3-yl-methyl) -phenylamino) -1-methylmethylene] -5 -amido- 2- indolinone (144) 3-Z-[l-(4-(7-methoxy-2,3,4,5-tetrahydrobenzo(d)azepin-3-yl-methyl) -phenylamino) -1-methylmethylene] -5-amido-2-indolinone 78 (145) 3-Z-[1-(4-(7-methyl-2,3,4,5-tetrahydrobenzo(d)azepin-3-yl-methyl) -phenylamino) -1-methylmethylene] -5-amido-2-indolinone (146) 3-Z-11-(4-(7,8-dimethoxy-2,3,4,5-tetrahydrobenzo azepin-3-y1-methyl) -phenylamino) -1-methylmethylene] -5-amido-2-indolinone (147) 3-Z-[1-(4-(6,7-dichloro-1,2,3,4-tetrahydroisoquinolin-2-yl-methyl) -phenylamino) -1-methyl-methylene] 5-amido-2 -indolinone (148) 3-Z-[1-(4-(6,7-dimethyl-1,2,3,4-tetrahydroisoquinolin-2-yl-methyl) -phenylamino) -1-methyl-methylene] 5-amido-2 -indolinone (149) 3-Z-[1-(4-(6,7-difluoro-1,2,3,4-tetrahydroisoquinolin-2-y1-methyl) -phenylamino) -1-methyl-methylene] 5-amido-2-indolinone (150) 3-Z--[1-(4-(6-chloro-1,2,3,4-tetrahydro-isoquinolin- 2-yl-methyl) -phenylamino) -1-methyl-methylene] -5-amido-2indol inane (151) 3-Z-t1-(4-(7-chloro-1,2,3,4-tetrahydro-isoquinolin- 2-yl-methyl) -phenylamino) -1-methyl-methylene] -5-amido-2indol inane (152) 3-Z-[1-(4-(6-methoxy-1,2,3,4-tetrahydro-isoquinolin- 2-y1-methyl) -phenylamino) -1-methyl-methylene] 2 -indolinone (153) 3-Z-[1-(4-(7-methoxy-1.,2,3,4-tetrahydro-isoquinolin- 2-yl-methyl) -phenylamino) -1-methyl-methylene] -5-amido-2indol inane 79 (154) 3-Z-[1-(4-(2,3,4,5-tetrahydro-azepino(4,5-b)pyrazin- 3-yl-methyl) -phenylamino) -1-methyl-methylene] 2- indolinone (155) 3-Z-[-(4-(7-Amino-2,3,4,5-tetrahydro-azepino(4,5b)pyrazin-3-y1-methyl) -phenylamino) -1-methyl-methylene] amido- 2- indolinone (156) 3-Z-[1-(4-(2-amino-5,6,7,8-tetrahydro-azepino(4,5d)thiazol-6-yl-methyl) -phenylamino) -1-methyl-methylene] amido-2 -indolinone (157) 3-Z-[l-(4-(5,6,7,8-tetrahydro-azepino(4,5-d)thiazol- 6-yl-methyl) -phenylamino) -1-methyl-methylene] 2-indolinone (158) 3-Z- [1-(pyridin-3-yl-amino) -1-methyl-methylene] amido-2 -indolinone (159) 3-Z-[1-(thiazol-2-yl-amino)-1-methyl-methylene] amido-2 -indolinone (160) 3-Z-[1-(benzimidazbl-2-yl-amino)-1-methyltnethylene] -5-amido-2-indolinone (161) 3-Z-[1-(5-methyl-isoxazol-3-y-amino)-1-methylmethylene] -5-amido-2-indolinone (162) 3-Z- [1-(imidazol-2-yl-amino) -1-methyl-methylene] 5-amido-2-indolinone (163) 3-Z-[1-(5-methyl-pyridin-2-yl-amino)-1-methylmethylene] -5-amido-2-indolinone (164) 3-Z-[1-(5-bromo-pyridin-2-yl-amino)-1-methylmethylene] -5-amido-2-indolinone 80 (165) 3-Z-[l-(2-chloro-pyridin-5-yl-amino)-l-methylmethylene]-5-amido-2-indolinone Example 2 3-Z-[1-(4-Diethylcarbamoyl-phenylamino)-1-methylmethvlene]-5-amido-2-indolinone 2 g of the resin prepared in Example IVb are reacted analogously to Example 1 with 2 g of ethyl 4-aminobenzoate in dimethylformamide at 110 0 C. The moist charged resin is suspended in 15 ml of dioxane and 15 ml of methanol and stirred with 12 ml of 1N sodium hydroxide solution for hours. Then the mixture is neutralised with dilute hydrochloric acid and washed with methylene chloride, methanol and dimethylformamide. 300 mg of the resin are then suspended in 3 ml of dimethylformamide and left to stand with 0.2 ml of diethylamine, 0.5 g of TBTU (Obenzotriazol-l-yl-N,N,N',N'-tetramethyluroniumtetrafluoroborate), and 0.8 ml of N-ethyl-diisopropylamine for 40 hours at ambient temperature. Finally, the product is cleaved from the resin as described in Example 1.

Yield: 61 mg, Rf value: 0.30 (silica gel, methylene chloride/methanol 9:1)

C

22

H

24 N403 mass spectrum: m/z 392 The following compounds are prepared analogously to Example 2: 3-Z-[1-(4-benzylcarbamoyl-phenylamino)-1-phenylmethylene]-5-amido-2-indolinone Prepared analogously to Example 2 with benzylamine Rf value: 0.30 (silica gel, methylene chloride/methanol 9:1)

C

25 H22N403 81 mass spectrum: m/z 426 3-Z-[1-(4-(N-methoxycarbonylmethyl-carbamoyl)phenylamino)-1-phenyl-methylene]-5-amido-2-indolinone Prepared analogously to Example 2 with glycinethyl ester R, value: 0.50 (silica gel, methylene chloride/methanol 9:1)

C

21

H

20 mass spectrum: m/z 408 (M 3-Z-[1-(4-dimethylcarbamoyl-phenylamino)-1-phenylmethylene]-5-amido-2-indolinone Prepared analogously to Example 2 with dimethylamine Rf value: 0.40 (silica gel, methylene chloride/methanol 9:1)

C

20

H

20

N

4 0 3 mass spectrum: m/z 364 3-Z-[1-(4-(N-(2-piperidino-ethyl)-carbamoyl)phenylamino)-1-methyl-methylene]-5-amido-2-indolinonetrifluoroacetate Prepared analogously to Example 2 with 1-(2-amino-ethyl)piperidine Rf value: 0.30 (silica gel, methylene chloride/methanol 4:1)

C

25

H

29

N

5 0 3 mass spectrum: m/z 448 3-Z-[1-(4-(N-methyl-piperazino-carbamoyl)phenylamino)-1-phenyl-methylene]-5-amido-2-indolinonetrifluoroacetate Prepared analogously to Example 2 with N-methyl-piperazine Rf value: 0.40 (silica gel, methylene chloride/methanol 4:1)

C

23

H

25

N

5 0 3 mass spectrum: m/z 419 (M 82 3-Z-[1-(4-(N-(2-Diethylamino-ethyl)-N-methylcarbamoyl)-phenylamino)-1-phenyl-methylene]-5-amido-2indolinone-trifluoroacetate Prepared analogously to Example 2 with N,N-diethyl-N'methyl-ethylenediamine R, value: 0.20 (silica gel, methylene chloride/methanol 4:1)

C

25

H

3 INs0 3 mass spectrum: m/z 449 3-Z-[1-(4-Butylcarbamoyl-phenylamino)-1-phenylmethylene]-5-amido-2-indolinone Prepared analogously to Example 2 with butylamine Rf value: 0.80 (silica gel, methylene chloride/methanol 4:1)

C

2

,H

24

N

4 0 3 mass spectrum: m/z 392 Example 3 3-Z-[1-(4-(N-methyl-N-benzoyl-amino)-phenylamino)-1methyl-methylene]-5-amido-2-indolinone g of a resin prepared according to Example IVb are reacted analogously to Example 1 with 3.4 g of 4-(9Hfluoren-9-yl-methoxycarbonyl)-methylamino)-aniline in dimethylformamide. Then the 9H-fluoren-9-ylmethoxycarbonyl group is cleaved with 40 ml of piperidine in dimethylformamide and the resin is washed several times. Then 400 mg of the resin are suspended in 4 ml of dimethylformamide and 0.3 ml of triethylamine and reacted with 0.3 ml of benzoylchloride for one hour at ambient temperature. Finally, the product is cleaved from the resin with trifluoroacetic acid as described in Example 1.

Yield: 25 mg, 83 Rf value: 0.51 (silica gel, methylene chloride/methanol 9:1) 24

N

4 03 mass spectrum: m/z 426 (M The following compounds are prepared analogously to Example 3: 3-Z-[1-(4-(N-methyl-N-propionyl-amino)-phenylamino)- 1-methyl-methylene]-5-amido-2-indolinone Prepared analogously to Example 3 with propionic acid chloride Rf value: 0.52 (silica gel, methylene chloride/methanol 9:1)

C

21

H

22

N

4 0 3 mass spectrum: m/z 378 (M 3-Z-[1-(4-(N-methyl-N-butyryl-amino)-phenylamino)- 1-methyl-methylene]-5-amido-2-indolinone Prepared analogously to Example 3 with butyric acid chloride Rf value: 0.28 (silica gel, methylene chloride/methanol 9:1)

C

22

H

24

N

4 0 3 mass spectrum: m/z 392 3-Z-[1-(4-(N-methyl-N-ethanesulphonyl-amino)phenylamino)-1-methyl-methylene]-5-amido-2-indolinone Prepared analogously to Example 3 with ethanesulphonic acid chloride Rf value: 0.30 (silica gel, methylene chloride/methanol 9:1)

C

2 0H 22

N

4 0 4

S

mass spectrum: m/z 413 3-Z-[1-(4-(N-methyl-N-propanesulphonyl-amino)phenylamino)-1-methyl-methylene]-5-amido-2-indolinone 84 Prepared analogously to Example 3 with propanesulphonic acid chloride Rf value: 0.31 (silica gel, methylene chloride/methanol 9:1)

C

21

H

24

N

4 0 4

S

mass spectrum: m/z 451 (M+Na') 3-Z-[1-(4-(N-methyl-N-phenylsulphonylamino)phenylamino-1-methyl-methylene]-5-amido-2-indolinone Prepared analogously to Example 3 with phenylsulphonic acid chloride Rf value: 0.46- (silica gel, methylene chloride/methanol 9:1)

C

24

H

22

N

4 0 4

S

mass spectrum: m/z 462 3-Z-[1-(4-(N-methyl-N-acetyl-amino)-phenylamino)-1methyl-methylene]-5-amido-2-indolinone Prepared analogously to Example 3 with acetylchloride Rf value: 0.20 (silica gel, methylene chloride/methanol 9:1)

C

20

H

2 N,4 03 mass spectrum: m/z 364'(M') 3-Z-[1-(4-(N-methyl-N-phenylmethylsulphonyl-amino)phenylamino)-1-methyl-methylene]-5-amido-2-indolinone Prepared analogously to Example 3 with phenylmethanesulphonic acid chloride R, value: 0.43 (silica gel, methylene chloride/methanol 9:1)

C

25

H

24

N

4 0 4

S

mass spectrum: m/z 475 85 Example 4 Methyl 3-Z-[1-(4-(N-benzyl-N-methyl-aminomethyl)phenylamino)-1-methyl-methylene]-2-indolinone-5carboxylate g (28 mmol) of methyl l-acetyl-3-(l-ethoxy-l-methylare dissolved in ml of dimethylformamide and stirred with 6.3 g (28 mmol) of 4-(N-benzyl-N-methyl-aminomethyl)-aniline for 6 hours at 80 0 C. Then 30 ml of conc. ammonia are added and the mixture is left to stand for 2 hours at 45 0 C. The solution is evaporated down and the residue is washed with ethanol and ether. Then it is chromatographed over a small silica gel column with ethyl acetate/ethanol Yield: 8.6 g (70 of theory), melting point: 150-152 °C

C

2

H

27

N

3 0 3

O

mass spectrum: m/z 442 The following compounds are prepared analogously to Example 4: methyl 3-Z-[1-(4-(piperidino-methyl)-phenylamino)-1-

C

24

H

27

N

3 0 3 mass spectrum: m/z 406 (M+H methyl 3-Z-[1-(4-bromo-phenylamino)-1-methyl-

C

18 HisBrN 2 0 3 mass spectrum: m/z 386/388 (M methyl 3-Z-[1-(4-chloro-phenylamino)-1-methyl-

C

18 HisC1N 2 0 3 mass spectrum: m/z 342/344 86 methyl 3-Z- (N-methyl-N-methylsulphonyl-amino) phenylamino) -1-ethyl -methylene]

C

20

H

21

N

3 0 5

S

mass spectrum: m/z 415 methyl 3-Z-[l-(4-(2,3,4,5-tetrahydro-benzo(d)azepin-3yl-methyl) -phenylamino) -1-methyl-methylene] -2-indolinone- S -carboxylate

C

29

H

29

N

3 0 2 mass spectrum: m/z 467 Example 3-Z- (N-benzyl-N-methyl-aminomethyl) -phenylamino) 1-methyl-methylenel -2-indolinone-5-carboxylic acid 2.3 g (5 mmol) of methyl 3-Z-[l-(4-(N-benzyl-N-methylaminomethyl) -phenylamino) -1-methyl-methylene] -2are dissolved in 50 ml of methanol and 50 ml of dioxane and stirred with 25 ml of lN sodium hydroxide solution for 1 hour at 70 0 C. Then the mixture is neutralised with 25 ml of 1N hydrochloric acid and evaporated to dryness. The residue is washed several times with water and dried.

Yield: 1.9 g (85 %6 of theory),

C

26

H

25

N

3 0 3 mass spectrum: m/z 428 The following compounds are prepared analogously to Example 3-Z-[Il- (Piperidino-methyl) -phenylamino) -1-methylmethylene] -2-indolinone-5-carboxylic acid

C

23

H

25

N

3 0 3 mass spectrum: m/z 392 87 3-Z- [1-(4-bromo-phenylamino) -1-methyl-methylene] -2acid 3-Z- [1-(4-chloro-phenylamino) -1-methyl-methylene] -2indolinone-5-carboxylic acid

C

17

H

1 3 C1N20 3 mass spectrum: m/z 327/329 3-Z- (N-methyl-N-methylsulphonyl-amino) phenylamino) -1-methyl-methylene] acid

C

19

H

19

N

3 0 5

S

mass spectrum: m/z 401 3-Z-[1-(4-(2,3,4,5-tetrahydro-benzo(d)azepin-3-ylmethyl) -phenylamino) -1-methyl-methylene] carboxylic acid

C

28 H27NO0 mass spectrum: m/z 453 Example 6 3-Z- (N-benzyl-N-methyl-aminomethyl) -phenylamino) .1-methyl-methylene] -2-indolinone-5-diethvlcarbamoyl-2indolinone 0.3 g of 3-Z- (N-benzyl-N-methyl-aminomethyl) phenylamino) -1-methyl-methylene] -2-indolinone-2acid are dissolved with 1.2 g of N-ethyl-diisopropylethylamine in 8 ml of dimethylformamide. Then 0.1 g of diethylamine and 0.4 g of TBTU (O-benzotriazol-l-yl-N,N,N' -tetramethyluroniumtetrafluoroborate) are added and the mixture is stirred f or 20 hours at ambient temperature. It is then evaporated down and the residue is suspended in water and extracted with methylene chloride. The organic phase is evaporated 88 down and chromatographed over a silica gel column with methylene chloride/ethanol (19:1).

Yield: 0.2 g (68% of theory), Rf value: 0.36 (silica gel, methylene chloride/ethanol 19:1)

C

30

H

3 4N402 mass spectrum: m/z 482 The following compounds are prepared analogously to Example 6: 3-Z-[l-(4-(Piperidino-methyl)-phenylamino)-1-methylmethylene]-2-indolinone-5-diethylcarbamoyl-2-indolinone Prepared from the compound produced in Example 5(1) and diethylamine C27H34N402 mass spectrum: m/z 446 3-Z-[l-(4-(N-methyl-N-methylsulphonyl-amino)phenylamino) -1-methyl-methylene diethylcarbamoyl-2-indolinone Prepared from the compound produced in Example 5(4) and diethylamine

C

23

H

28

N

4 0 4

S

mass spectrum: m/z 457 3-Z-[l-(4-(2,3,4,5-tetrahydro-benzo(d)azepin-3-ylmethyl) diethylcarbamoyl-2-indolinone 3-Z-[1-(4-(2,3,4,5-tetrahydro-benzo(d)azepin-3-ylmethyl) dimethylcarbamoyl-2-indolinone 3-Z-[1-(4-(N-Phenylmethyl-N-methylamino-methyl)phenylamino)-l-methyl-methylene]-5-methylcarbamoyl-2- 89 indolinone 3-Z- (N-Phenylmethyl-N-methylamino-methyl) phenylamino) -1-methyl-methylene] -5-dimethylcarbamoyl-2indolinone 3-Z- (N-Phenylmethyl-N-methylamino-methyl) phenylamino) -1-methyl-methylene] -5-diethylcarbamoyl-2indol inane 3-Z- (N-Phenylmethyl-N-methylamino-methyl) phenylamino) -1-methyl-methylene] -5-propylcarbamoyl-2indolinone 3-Z- (N-Phenylmethyl-N-methylamino-methyl) phenylamino) -1-methyl-methylene] -5-dipropylcarbamoyl-2indolinone 3-Z- (direthylamino-methyl) -phenylamino) -1methyl-methylene] -5-methylcarbamoyl-2-indolinone (11) 3-Z- (dimethylantino-methyl) -phenylamino) -1methyl-methylene] -5-dimethylcarbamoyl-2-indolinone (12) 3-Z- (dimethylamino-methyl) -phenylamino) -1methyl-methylene] -5-diethylcarbamoyl-2-indolinone (13) 3-Z-[11- (dimethylamino-methyl) -phenylamino) -1methyl-methylene] -5-propylcarbamoyl-2-indolinone (14) 3-Z- (dimethylarnino-methyl) -phenylamino) -1methyl-methylenel -5-dipropylcarbamoyl-2-indolinone 3-Z- (dimethylamino-methyl) -phenylamino) -1methyl-methylene] -5-methylcarbamoyl-2-indolinone 90 (16) 3-Z- (dimethylamino-methyl) -phenylamino) -1methyl-methylene] -5-dimethylcarbamoyl-2-indolinone (17) 3-Z- (dimethylamino-methyl) -phenylamino) -1methyl-methylene] -5-diethylcarbamoyl-2-indolinone (18) 3-Z- (dimethylamino-methyl) -phenylamino-1methyl-methylene] -5-propylcarbamoyl-2-indolinone (19) 3-Z- (direthylamino-methyl) -phenylamino) -1methyl-methylene] -5-dipropylcarbamoyl-2-indolinone 3-Z- [1-(4-chioro-phenylamino) -1-methyl-methylene] -methylcarbamoyl indolinone (21) 3-Z- [1-(4-chloro-phenylamino) -1-methyl-methylene] dimethylcarbamoyl indolinone (22) 3-Z- [1-(4-chioro-phenylamino) -i-methyl-rnethylene] diethylcarbamoyl-2-indolinone (23) 3-Z- [1-(4-chioro-phenylamino) -1-methyl-methylene] propyl carbamoyl indol inone (24) (4-chioro-phenylamino) -1-methyl-methylene] dipropylcarbamoyl indolinone 3-Z- (1-phenylamino-1-methyl-methylene) methyilcarbamoyl indol inone (26) 3-Z- (i-phenylamino-1-methyl-methylene) dimethylcarbamoyl indolinone (27) 3-Z- (l-Phenylamino-1-methyl-methylene) diethylcarbamoyl-2-indolinone 91 Example 7 3-Z-[1-(4-methyl-3-amino-phenylamino)-1-methyl-methylene]- 5-amido-2-indolinone 130 mg of 3-Z-[1-(4-methyl-3-nitro-phenylamino)-1-methylmethylene]-5-amido-2-indolinone are dissolved in 9 ml of methanol and hydrogenated with 50 mg of Raney nickel at ambient temperature under 3 bar of hydrogen pressure. The catalyst is filtered off and the solution is evaporated down.

Yield: 97 mg (70 of theory), Rf value: 0.60- (silica gel, methylene chloride/Ethanol 4:1)

C

18

,H

1

N

4 0 2 mass spectrum: m/z 322 The following compound is prepared analogously to Example 7: 3-Z-[1-(4-(piperidino-methyl)-3-amino-phenylamino)-1methyl-methylene]-5-amido-2-indolinone Prepared aus 3-Z-[1-(4-(piperidino-methyl)-3-nitro-phenylamino)-1-methyl-methylene]-5-amido-2-indolinone Rf value: 0,15 (silica gel, methylene chloride/ethanol 9:1)

C

23

H

27

N

5 0 2 mass spectrum: m/z 406

J

92 Example 8 Dry ampoule containing 75 mg of active substance per 10 ml Composition: Active substance Mannitol water for injections 75.0 mg 50.0 mg ad 10.0 ml Preparation: Active substance and mannitol are dissolved in water.

After packaging the solution is freeze-dried. To produce the solution ready for use, the product is dissolved in water for injections.

Example 9 Dry ampoule containing 35 mg of active substance per 2 ml Composition: Active substance Mannitol water for injections 35.0 mg 100.0 mg ad 2.0 ml Preparation: Active substance and mannitol are dissolved in water.

After packaging, the solution is freeze-dried.

To produce the solution ready for use, the product is dissolved in water for injections.

93 Example Tablet containing 50 mg of active substance Composition: Active substance Lactose Maize starch Polyvinylpyrrolidone Magnesium stearate 50.0 mg 98.0 mg 50.0 mg 15.0 mg 2.0 mg 215.0 mg Preparation: and are mixed together and granulated with an aqueous solution of is added to the dried granulated material. From this mixture tablets are pressed, biplanar, faceted on both sides and with a dividing notch on one side.

Diameter of the tablets: 9 mm.

Example 11 Tablet containing 350 mg of active substance Composition: Active substance Lactose Maize starch Polyvinylpyrrolidone Magnesium stearate 350.0 mg 136.0 mg 80.0 mg 30.0 mg 4.0 mc 600.0 mg (lI 94 Preparation: and are mixed together and granulated with an aqueous solution of is added to the dried granulated material. From this mixture tablets are pressed, biplanar, faceted on both sides and with a dividing notch on one side.

Diameter of the tablets: 12 mm.

Example 12 Capsules containing 50 mg of active substance Composition: Active substance Dried maize starch Powdered lactose Magnesium stearate 50.0 mg 58.0 mg 50.0 mg 2.0 mq 160.0 mg Preparation: is triturated with This trituration is added to the mixture of and with vigorous mixing.

This powder mixture is packed into size 3 hard gelatin capsules in a capsule filling machine.

95 Example 13 Capsules containing 350 mg of active substance Composition: Active substance Dried maize starch Powdered lactose Magnesium stearate 350.0 mg 46.0 mg 30.0 mg 4.0 mq 430.0 mg Preparation: is triturated with This trituration is added to the mixture of and with vigorous mixing.

This powder mixture is packed into size 0 hard gelatin capsules in a capsule filling machine.

Example 14 Suppositories containing 100 mg of active substance 1 suppository contains: Active substance Polyethyleneglycol 1500) Polyethyleneglycol 6000) Polyethylenesorbitan monostearate 100.0 mg 600.0 mg 460.0 mg 840.0 mg 2,000.0 mg Preparation: The polyethyleneglycol is melted with the polyethylenesorbitan monostearate. The milled active substance is 9- 7-03;17:48 10/ 36 -96homogeneously dispersed in the melt at 40*C. The melt is cooled to 38 0 C and poured into lightly pre-cooled suppository moulds.

Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step

S

10 or group of integers or.steps but not the exclusion of any other integer or step or group of integers or steps.

4 The reference to any prior art in this specification is not, and should not be taken as, an acknowledgment or any form or suggestion that that prior art forms part of the common general knowledge in Australia.

COMS ID No: SMBI-00327262 Received by IP Australia: Time 18:02 Date 2003-07-09

Claims

9- 7-03;17:48 97 THE CLAIMS DEFINING THE INVENTION ARE AS FOLLOWS: 1. Substituted indolinones of general formula 11/ 36 R4 -N- ,ee8 wherein X denotes an oxygen or sulphur atom, R, denotes a hydrogen atom, a C 1 .4-alkoxy-carbonyl or C,.4-alkanoyl group, R, denotes a carboxy or C-. 4 -alkoxy-carbonyl group or an aminocarbonyl group optionally substituted by one or two C_,-alkyl groups, whilst the substituents may be identical or different, R, denotes a hydrogen atom or a C,.,-alkyl group which may be substituted at the 2 position, in relation to the carbon atom of the R 3 group by a fluorine, chlorine or bromine atom, by a hydroxy, C_.,-alkoxy, Cz.,-alkylsulphenyl, -alkylsulphinyl, C,.,-alkylsulphonyl, phenylsulphenyl, phenylsulphinyl, phenylsulphonyl, amino, C 1 3 -alkylamino, di-(C 1 ,_-alkyl)-amino, C 2 .s-alkanoylamino or N- (C._-alkylamino) 6 -alkanoylamino group, COMS ID No: SMBI-00327262 Received by IP Australia: Time 18:02 Date 2003-07-09 1' I. 98 R 4 denotes a hydrogen atom, a C._g-alkyl group or a Cs_,-Cycloalkyl group optionally substituted by a C 1 3 -alkyl group wherein a methylene group in the 3 or 4 position in relation to the carbon atom of the R 3 -C(R 4 NRs)= group may be substituted by an imino group optionally substituted by a C 1 3 -alkyl group, a phenyl or naphthyl group which may be substituted by a fluorine, chlorine, bromine or iodine atom, by a methoxy group optionally substituted by 1 to 3 fluorine atoms, by a C 2 3 -alkoxy which may be substituted in the 2 or 3 position by a C 1 3 -alkylamino, di-(Cl_ 3 -alkyl)-amino or to 7-membered cycloalkyleneimino group, whilst additionally an alkyl moiety in the abovementioned alkylamino and dialkylamino groups may be substituted by a phenyl group, by a trifluoromethyl, amino, C 13 -alkylamino, di- (Ci_ 3 -alkyl) -amino, C 2 alkanoylamino, N-(C 1 -3-alkyl)- C 2 -5-alkanoylamino, C 1 _s-alkylsulphonylamino, N- (C 1 3 -alkyl)- Cls-alkylsulphonylamino, phenylsulphonylamino, N- (C 1 3 alkyl) -phenylsulphonylamino, aminosulphonyl, C_ 3 -alkylaminosulphonyl or di-(C_ 3 -alkyl) -aminosulphonyl group, whilst additionally an alkyl moiety in the abovementioned alkylamino and dialkylamino groups may be substituted by a phenyl group, by a carbonyl group which is substituted by a hydroxy, C _3-alkoxy, amino, C 1 _3-alkylamino or N-(C 1 _s-alkyl)- Cl_ 3 -alkylamino group, whilst additionally an alkyl moiety in the abovementioned groups may be substituted by a carboxy, C_ 3 -alkoxycarbonyl or phenyl group or in the 2 or 3 position by a di-(C,3-alkyl)-amino, piperazino,
99- N-(C 1 3 -alkyl)-piperazino or 5- to 7-membered cyc- loalkyleneimino group, by a C,- 3 -alkyl group which is substituted by an amino, C 7 _,-alkylamino, C 5 -cycloalkylamino or phenyl- CI_ 3 -alkylamino group which may additionally be substituted at the amino nitrogen atom by a C,3-alkyl group wherein the hydrogen atoms are wholly or partially replaced by fluorine atoms, by a C 5 ,--cycloalkyl, C2-4-alkenyl or Cl 4 -alkyl group, whilst the abovementioned C 1 4 -alkyl substituent may in each case be additionally mono, di- or trisubstituted by a cyano, carboxy, C 1 3 -alkoxycarbonyl, pyridyl, imidazolyl, benzo[l,3]dioxole or phenyl group, wherein the phenyl group may be substituted by fluorine, chlorine or bromine atoms, by methyl, methoxy, trifluoromethyl, cyano or nitro groups and the substituents may be identical or different, or may be substituted in the 2, 3 or 4 position by a hydroxy group, by a C 1 3 -alkyl group which may be substituted by a hydroxy, carboxy, thiomorpholino, 1-oxido- thiomorpholino, 1,1-dioxido-thiomorpholino, piperazino, N- (C, 3 -alkyl) -piperazino or N-phenyl-piperazino group, by a 5- to 7-membered cycloalkenyleneimino group or by a 4- to 7-membered cycloalkyleneimino group, wherein the abovementioned 5- to 7-membered cycloalkyleneimino groups may be substituted by one or two C, 3 -alkyl groups, by a C,_-cycloalkyl or phenyl group, by a C 1 3 -alkyl, C 5 7 -cycloalkyl, phenyl, carboxy or C,_ 4 -alkoxy-carbonyl group and by a hydroxy group and in the abovementioned cycloalkyleneimino groups a methylene group adjacent to the nitrogen atom may be replaced by a carbonyl group, 9- 7-03;17:48 12/ 36 100 by a C 13 -alkyl group which is substituted by a 5- to 7- membered cycloalkyleneimino group, whilst a phenyl group optionally mono- or disubstituted by fluorine, chlorine or bromine atoms or by methyl or methoxy groups, wherein the substituents may be identical or different, or an oxazolo, imidazolo, thiazolo, pyridino, pyrazino or pyrimidino group, optionally substituted by a fluorine, chlorine, bromine or iodine atom or by a methyl, methoxy or amino group, may be fused to the abovementioned 5- to 7-membered cycloalkyleneimino groups via two adjacent carbon atoms, whilst additionally the abovementioned monosubstituted r phenyl groups may be substituted by a fluorine, chlorine 15 or bromine atom or by a methyl, methoxy or nitro group, a 5-membered heteroaromatic group which contains an imino group, an oxygen or sulphur atom or an imino group, an oxygen or sulphur atom and one or two nitrogen atoms, or 1 a 6-membered heteroaromatic group which contains one, two r or three nitrogen atoms, whilst the abovementioned 5- and 6-membered heteroaromatic groups may additionally be •substituted by a chlorine or bromine atom or by a methyl group, or a phenyl ring may be fused to the abovementioned 5- or 6-membered heteroaromatic groups via two adjacent carbon atoms, and RS denotes a hydrogen atom or a C.,-alkyl group whilst any carboxy, amino or imino groups present may be substituted by groups which can be cleaved in vivo, COMS ID No: SMBI-00327262 Received by IP Australia: Time 18:02 Date 2003-07-09 9- 7-03:17:48 13/ 36 100A the stereoisomers and salts thereof, with the proviso that if X denotes an oxygen atom and RI and R 5 each denote an hydrogen atom, R 4 may not denote a 'phenyl group which is substituted by an CI.3-alkylamino, di-(C 1 3 alkyl) amino, C 1 -5-alkylsulphonylamino, phenylsulphonylamino, aminosulphonyl, CI-3 alkylaminosulphonyl, di- (C- 3 alkyl) aminosulphonyl or N-(C1-s-alkyl)-Ci-3 alkylaminocarbonyl group. q to *o 9* **e COMS ID No: SMBI-00327262 Received by IP Australia: Time 18:02 Date 2003-07-09 101 2. Substituted indolinones of general formula I according to claim 1, wherein X denotes an oxygen atom, RI denotes a hydrogen atom, R 2 denotes an aminocarbonyl group, R 3 denotes a hydrogen atom or a C 1 4 -alkyl group which may be substituted, at the 2 position in relation to the carbon atom of the R3--C(R 4 NR) group, by a chlorine or bromine atom or by a phenylsulphonyl group, R 4 denotes a hydrogen atom, a C 1 3 -alkyl group or a cyclopentyl or cyclohexyl group optionally substituted by a methyl group, whilst in the cyclopentyl and cyclohexyl group a methylene group in the 3 or 4 position in relation to the carbon atom of the R 3 -C(R 4 NRs)= group may be replaced by an imino group optionally substituted by a methyl group, a phenyl group which is substituted by a fluorine, chlorine, bromine or iodine atom, by a methoxy group optionally substituted by 1 to 3 fluorine atoms, by a C2- 3 -alkoxy which is substituted in the 2 or 3 position by methylamino, dimethylamino or 5- to 7- membered cycloalkyleneimino group, whilst additionally a methyl group in the abovementioned amino groups may be substituted by a phenyl group, by a trifluoromethyl, amino, C2-.-alkanoylamino, N-(C 13 -alkyl)-C2- 5 -alkanoylamino, Ci_-alkylsulphonylamino, N-(C 1 3 -alkyl)- 102 Cls-alkylsulphonylamino, phenylsulphonylamino, N-(C 13 -alkyl)-phenylsulphonylamino or aminosulphonyl group, whilst additionally an alkyl moiety in the abovementioned alkylamino and dialkylamino groups may be substituted by a phenyl group, by a carbonyl group which is substituted by a hydroxy, C 1 3 -alkoxy, amino, C 1 3 -alkylamino or N- (CIs-alkyl)- C 13 -alkylamino group, whilst additionally an alkyl moiety in the abovementioned groups may be substituted by a carboxy, C,_ 3 -alkoxycarbonyl or phenyl group or in the 2 or 3 position by a di-(C 1 3 -alkyl)-amino, pipera- zino, N-(C 1 _3-alkyl)-piperazino or 5- to 7-membered cyc- loalkyleneimino group, by a C 1 3 -alkyl group which is substituted by an amino, CI_ 7 -alkylamino, Cs_,-cycloalkylamino or phenyl- C 13 -alkylamino group which may additionally be substituted at the amino nitrogen atom by a C.3 -alkyl group wherein the hydrogen atoms are wholly or partially replaced by fluorine atoms, by a cyclohexyl, C 24 -alkenyl or CI_ 4 -alkyl group, whilst the abovementioned C,_4-alkyl substituent may in each case be additionally substituted by a cyano, carboxy, C_ 3 -alkoxycarbonyl, pyridyl, imidazolyl, benzo[1,3]dioxole or phenyl group, wherein the phenyl group may be monosubstituted by a fluorine, chlorine or bromine atom or by a methyl, methoxy, cyano, trifluoromethyl or nitro group, or di- or trisubstituted by fluorine, chlorine or bromine atoms or by methyl or methoxy groups, and the substituents may be identical or different, or may be substituted in the 2, 3 or 4 position by a hydroxy group, by a C 1 _3-alkyl group which may be substituted by a hydroxy, carboxy, thiomorpholino, 1-oxido- 9- 7-03;17:48 14/ 36 103 thiomorpholino, 1,1-dioxido-thiomorpholino, piperazino, N- 3 -alkyl) -piperazino or N-phenyl-piperazino group, by a 5- to 7-membered cycloalkenyleneimino group or by a 4- to 7-membered cycloalkyleneimino group, wherein the abovementioned 5- to 7-membered cycloalkyleneimino groups may be substituted by one or two C.,-alkyl groups, by a cyclohexyl or phenyl group, by a C,-a-alkyl, cyclohexyl, phenyl, carboxy or C,. 4 -alkoxy-carbonyl group and by a hydroxy group and in the abovementioned cycloalkyleneimino groups a methylene group adjacent to the nitrogen atom may be replaced by a carbonyl group, by a C ,-alkyi group which is substituted by a 5- to 7- membered cycloalkyleneimino group, whilst a phenyl group 15 optionally mono- or disubstituted by fluorine, chlorine or bromine atoms or by methyl or methoxy groups, wherein the substituents may be identical or different, or a pyrazino or thiazolo group, optionally substituted by an amino group, may be fused to the abovementioned 5- to 7- 20 membered cycloalkyleneimino groups via two adjacent carbon atoms, Swhilst additionally the abovementioned monosubstituted phenyl groups may be substituted by a fluorine, chlorine or bromine atom or by a methyl, methoxy or nitro group, a pyridyl group optionally substituted by a chlorine or bromine atom or by a methyl group, an oxazolyl, isoxazolyl, imidazolyl or thiazolyl group optionally substituted by a methyl group, to which a phenyl ring may be fused via two adjacent carbon atoms, and R, denotes a hydrogen atom or a C, ,-alkyl group, COMS ID No: SMBI-00327262 Received by IP Australia: Time 18:02 Date 2003-07-09 9- 7-03:17:48 -103A the sterecisomers and salts thereof, with the proviso that if XC denotes an oxygen atom and R, and R 5 each denote an hydrogen atom, R 4 may not denote a phenyl group which is substituted by an C 16 phenylsulphonylamino, aminosuJlphonyl or N- (C 15 -alkylJ -C 1 3 alkylaminocarbonyl group. 15/ 36 *to COMS ID No: SMBI-00327262 Received by IP Australia: Time 18:02 Date 2003-07-09 9- 7-03;17:48 16/ 36 104 3. Substituted indolinones of general formula I according to claim 2, wherein R 2 is in the 5 position, the stereoisomers and the salts thereof. 4. Substituted indolinones of general formula I according 10 to claim 1, wherein X denotes an oxygen atom, R, denotes a hydrogen atom, R, in the 5 position denotes an aminocarbonyl group, R, denotes a hydrogen atom or a C .,-alkyl group which may be terminally substituted by a chlorine or bromine atom or 20 by a phenylsulphonyl group, R 4 denotes a hydrogen atom, a C. 3 ,-alkyl group or a cyclopentyl or cyclohexyl group optionally substituted by a methyl group, whilst in the cyclohexyl group a methylene S. 25 group in the 4 position in relation to the carbon atom of the R 3 -C(R 4 NR 5 group may be replaced by an imino group optionally substituted by a methyl group, a phenyl group which may be substituted by a fluorine, chlorine, bromine or iodine atom, by a methyl or ethyl group, which may in each case be substituted by a c -alkylamino, di- (C,.,-alkyl)-amino, thiomorpholino, 1-oxido-thiomorpholino, 1,1-dioxido- thiomorpholino, N-phenyl-piperazino, 5- to 6-membered cycloalkenyleneimino group or by a 5- to 7-membered COMS ID No: SMBI-00327262 Received by IP Australia: Time 18:02 Date 2003-07-09 9- 7-03 17:48 17/ 36 105 cycloalkyleneimino group, whilst the abovementioned 5- to 7-membered cycloalkyleneimino groups may be substituted by one or two methyl groups, by a cyclohexyl or phenyl group, by a methyl, cyclohexyl or phenyl group and by a hydroxy group, or by a methyl or ethyl group which may be substituted by a phenyl group which is substituted by a 5 to 7-membered cycloalkyleneimino group, whilst additionally a phenyl ring is fused to the abovementioned cycloalkyleneimino groups via 2 adjacent carbon atoms, by a methyl or ethyl group substituted by an amino, methylamino or ethylamino group, each of which is additionally substituted at the amino nitrogen atom by a benzyl or phenylethyl group, wherein the phenyl moiety in the abovementioned groups may be monosubstituted by a fluorine, chlorine or bromine atom or by a methyl, methoxy, cyano, trifluoromethyl or nitro group or di- or trisubstituted by fluorine, chlorine or bromine atoms or S* by methyl or methoxy groups, and the substituents may be identical or different, o* whilst additionally the abovementioned monosubstituted 25 phenyl groups may be substituted.by a fluorine, chlorine or bromine atom or by a methyl, methoxy or nitro group, and R 5 denotes a hydrogen atom or a C~,-alkyl group, the stereoisomers and the salts thereof. Substituted indolinones of general formula I according to claim 1, wherein X denotes an oxygen atom, COMS ID No: SMBI-00327262 Received by IP Australia: Time 18:02 Date 2003-07-09 106 RI denotes a hydrogen atom, R 2 in the 5 position denotes an aminocarbonyl group, R 3 denotes a hydrogen atom or a C 1 _4-alkyl group, R 4 denotes a phenyl group which may be substituted by a fluorine, chlorine, bromine or iodine atom, by a methyl or ethyl group, which may be substituted in each case by a C 13 -alkylamino, di-(C 1 3 -alkyl)-amino, thiomorpholino, 1-oxido-thiomorpholino, 1,1-dioxido- thiomorpholino, N-phenyl-piperazino, 5- to 6-membered cycloalkenyleneimino group or by a 5- to 7-membered cycloalkyleneimino group, whilst the abovementioned 5- to 7-membered cycloalkyleneimino groups may be substituted by one or two methyl groups, by a cyclohexyl or phenyl group, by a methyl, cyclohexyl or phenyl group and by a hydroxy group, or by a methyl or ethyl group which may be substituted by a phenyl group which is substituted in the 4 position by a to 7-membered cycloalkyleneimino group, whilst additionally a phenyl ring is fused to the abovementioned cycloalkyleneimino groups via 2 adjacent carbon atoms, by a methyl or ethyl group substituted by an amino, methylamino or ethylamino group, each of which is additionally substituted at the amino nitrogen atom by a benzyl or phenylethyl group, and wherein the phenyl moiety may be monosubstituted by a fluorine, chlorine or bromine atom or by a methyl, methoxy, cyano, trifluoromethyl or nitro group, disubstituted by methyl or methoxy groups or trisubstituted by methyl or methoxy groups, and the substituents may be identical or different, 9- 7-03:17:48 #8/3 1 S/ 3 6 107 whilst additionally the abovementioned ronosubstituted phenyl groups may be substituted by a fluorine, chlorine or bromine atom or by a methyl, methoxy or nitro group, and R, denotes a hydrogen atom or a C 3 4 -alkyl group, the stereoisomers and the. salts thereof. 6. The following gubstituted indolinones of general formula I according to claim 1: 3-2-L- (4-piperidinomethyl-phelamilo) methyl-methy- eq..is lane] -5-amido-2-indolinone, 3-2- [i-(4-bromo-phenylamino) -1-methyl-methylene] arido-2-indolinone, 3-2-El- (4-piperidiniomethyl-phenylanino) -1-butyl- methyJlenel -5-amido-2-indolinone. 3-Z-[Il- (4-chlorophenylamino) -i-methyl-methylene] amido-2-indolinone and 3-Z- (1-phenylamino-methylene) -5-amido-2-indolinole (N-benzyl-N-methyl-aminomethyl) phenylamino) -1-methyl-methylene] -5-amido-2-indolinone, 3-z- (4-chlorobenzyl) -aminomethyl) phenylamino) -1-methyl-methylene) -S-amido-2-indolinone, 3-Z- El- (N-benzyl-N-ethyl-arninomethyl) -phenylamil]- 1-methyl-methylene] -5-amido-2-indolinonle, COMS ID No: SMBI-00327262 Received by IP Australia: Time 18:02 Date 2003-07-09 9- 7-03:17:!48 #9/3 19 1/ 3 6 102 3-Z-(1-C4- (N-benzyl-aminonethyl) -phenylamJno) -1- methyl-rnethylenej -5-amido-2-indolinone, 3-Z-I:i- (N-benazyl-N-methyl-aminomethyl)- S phenylamnino) -methylene) -5-amido-2-indolinone, l-(4-(2,3,4,5-te-trahydro-ben-zo(d)azepin-3-yl- methyl) -phenylamino) -1-methyl-methylene] -5-amido-2- indol inone, 3-Z- [1-(4-piperidinomethyl-3-nitro-phenylamino) 1-methyl-methylene] -S-amido-2-indolinone and 3-Z- l(1C4-methyl-3-nitro-phenylamino) -1-methyl- methylene) -5-amido-2-indolinone as well as the sterecisomers and the salts thereof.. 7. (N-Benzyl-N-methyl-aminonethyl)- phenylamino) -1-methyl-methylene) -5-amido-2-indolinone and the salts thereof. a. 3-Z-[1-(4-(2,3,4,5-.Tetrahydro-benzo(d)azepin-3-yl- methyl) -phenylamino) -1-methyl-methylene] -5-amido-2- 0 25 indolinone and the salts thereof. .0.0 9. Physiologically acceptable salts of the compounds according to any one of claims 1 to B. 0. haaeucAl compositions con1taining a compouqnd according to-any one of claims 1 to 8 or a salt accor-ding to claim 9 and optionally o~ne or more inert carriers and/or diluents. 3S 11. Use of a compound according to any one of claims 1 to 8 or a salt according to claim 9 for prepar~ing COMS ID No: SMBI-00327262 Received by IP Australia: Time 18:02 Date 2003-07-09 9- 7-03;17:48 20/ 36 109 a pharmaceutical composition which is suitable for treating excessive or anomalous cell proliferation. 12. Process for preparing a pharmaceutical composition according to claim 10, wherein a compound according to any one of claims 1 to 8 or a salt according to claim 9 is incorporated in one or more inert carriers and/or diluents by a non-chemical method. 3 13. Process for preparing the compounds according to any one of claims 1 to 9, wherein °ooo• 0000 •go• a. a compound of general formula Z3 (II) *0 *e 0 0000 00.o 0 ago• 0 *990 0000 oo *0 0 wherein. X and R, are defined as in claims 1 to 8, has the meanings given for R, in claims 1 to 8, R, denotes a hydrogen atom or a protecting group for the nitrogen atom of the lactam group, whilst one of the groups or R, may also denote a bond to a solid phase optionally formed via a spacer and the other group or R, is as hereinbefore defined, and Z, denotes a halogen atom, a hydroxy, alkoxy or aralkoxy group, is reacted with an amine of general formula COMS ID No: SMBI-00327262 Received by IP Australia: Time 18:02 Date 2003-07-09 110 Rs H N (III), R4 wherein R 4 and R s are defined as in claims 1 to 8, and if necessary any protecting group used for the nitrogen atom of the lactam group is cleaved or a compound thus obtained is cleaved from a solid phase, or b. in order to prepare a compound of general formula I wherein R 2 denotes one of the aminocarbonyl groups mentioned in claims 1 to 8, a compound of general formula R3 R4 -N HO-CO R0 (IV), RI wherein R I and R 3 are defined as in claims 1 to 6, or a reactive derivative thereof, is amidated with an amine of general formula H (R 7 NR,) (V) wherein R 7 and R 8 which may be identical or different denote hydrogen atoms or C 1 3 -alkyl groups, and subsequently, if desired, a compound of general formula I thus obtained which contains an alkoxycarbonyl group may be converted by hydrolysis into a corresponding carboxy compound, or 9- 7-03;17:48 21/ 36 111 a compound of general formula I thus obtained which contains an amino or alkylamino group may be converted by alkylation or reductive alkylation into a corresponding alkylamino or dialkylamino compound, or a compound of general formula I thus obtained which contains an amino or alkylamino group may be.converted by acylation into a corresponding acyl compound, or a compound of general formula I thus obtained which contains a carboxy group may be converted by esterification or amidation into a corresponding ester or aminocarbonyl compound, or a compound of general formula I thus obtained which contains a nitro group is converted by reduction into a corresponding amino compound, or 20 if necessary any protecting group used during the reactions to protect reactive groups is cleaved, or a compound of general formula I thus obtained is resolved i into the stereoisomers thereof, or "25 0 o COMS ID No: SMBI-00327262 Received by IP Australia: Time 18:02 Date 2003-07-09 9- 7-03;17:48 22/ 36 rO1LlPhJ37i7-99asabntDc-WOPlirn -112- a compound of general formula I thus obtained is converted into the salts thereof, with an inorganic or organic acid or base. 14. The process according to claim 13 wherein the compound of general formula I.thus obtained is converted into the physiologically acceptable salts thereof. S@OO 15. Use of a compound according to any one of claims 1 to 8 ooo 10 or a salt according to claim 9 or a composition according to claim 10 for treating excessive or anomalous cell proliferation. 16. Use of a compound according to any one of claims 1 to 8 or a salt according to claim 9 in the manufacture of a medicament for the treatment of excessive or abnormal cell proliferation. 17. Substituted indolinones according to claim 1 20 substantially as hereinbefore described with reference to the Examples. DATED this 9th day of July, 2003 Boehringer Ingelheim Pharma KG by DAVIES COLLISON CAVE Patent Attorneys for the Applicant COMS ID No: SMBI-00327262 Received by IP Australia: Time 18:02 Date 2003-07-09