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FI95259B - Förfarande för framställning av farmaceutiskt aktiva 7-substituerade-2-amino-3,5-dihydro-4H-pyrrolo/3,2-d/pyrimidin-4-oner - Google Patents

Förfarande för framställning av farmaceutiskt aktiva 7-substituerade-2-amino-3,5-dihydro-4H-pyrrolo/3,2-d/pyrimidin-4-oner Download PDF

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Publication number
FI95259B
FI95259B FI914015A FI914015A FI95259B FI 95259 B FI95259 B FI 95259B FI 914015 A FI914015 A FI 914015A FI 914015 A FI914015 A FI 914015A FI 95259 B FI95259 B FI 95259B
Authority
FI
Finland
Prior art keywords
formula
amino
pyrimidin
dihydro
pyrrolo
Prior art date
Application number
FI914015A
Other languages
English (en)
Finnish (fi)
Other versions
FI95259C (sv
FI914015A0 (sv
Inventor
Iii John A Secrist
Mark David Erion
John A Montgomery
Steven E Ealick
Original Assignee
Biocryst Pharm Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Biocryst Pharm Inc filed Critical Biocryst Pharm Inc
Publication of FI914015A0 publication Critical patent/FI914015A0/sv
Publication of FI95259B publication Critical patent/FI95259B/sv
Application granted granted Critical
Publication of FI95259C publication Critical patent/FI95259C/sv

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/06Antigout agents, e.g. antihyperuricemic or uricosuric agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

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  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Immunology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Transplantation (AREA)
  • Dermatology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Compounds Of Unknown Constitution (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Claims (5)

1 H /A. N HN Y--\ (I) 10 \ AAV h2n n CHjAr 15 vari (a) -CHjAr är R R 1 2 väri (i) R, är väte, halogen, C,-C3-alkyl, C,-C3-alkoxi, bensyloxi eller hydroxi och R2 är väte, halogen, C,-C3-alkyl,
20 C,-C3-alkoxi, bensyloxi eller hydroxi, (ii) R, är väte eller C,-C3-alkyl och R2 är trifluormetyl eller (iii) R, är tri-fluormetyl och R2 är väte eller C,-C3-alkyl; eller (b) -CH2Ar är f^CH~ \ / x 25 väri X är svavel eller syre och vari anslutningen till tio-fen- eller furanringen är i 2- eller 3-positionen; eller en tautomer därav, kannetecknat av att en forening med formeln li 27 95259 H r3o2c. .n. (V) R4CNH-C=N CHjAr Il I 10. sr5 väri Ar har ovan angiven betydelse, R3 är lägre alkyl, R4 är karbocyklisk aryl, säsom fenyl, och Rs är lägre alkyl, kon-denseras genom att omsätta denna förening med vattenfri am-15 moniak och cykliseras vid förhöjd temperatur, varvid man erhäller en förening med formeln I, och om sä önskas, i) debensyleras en förening med formeln I, väri R] och/el-ler R2 är bensyloxi, varvid man erhäller motsvarande förening med formeln I, väri Rj och/eller R2 är hydroxi, eller 2 0 ii) dehalogeneras en förening med formeln I, väri R, och/el ler R2 är halogen, varvid man erhäller motsvarande förening med formeln I, väri R, och/eller R2 är väte.
1. Förfarande för framställning av en farmaceutiskt aktiv 7-substituerad-2-amino-3,5-dihydro-4H-pyrrolo[3,2-d]pyrimi-din-4-on med formeln 5 0
2. Förfarande enligt patentkrav 1, kannetecknat av att man 25 framställer 2-amino-3,5-dihydro-7-(3-klorfenylmetyl)-4H-pyr- rolo[3,2-d]pyrimidin-4-on.
3. Förfarande enligt patentkrav 1, kannetecknat av att man framställer 2-amino-3,5-dihydro-7 -(fenylmetyl)-4H-pyrrolo- 30 [3,2-d]pyrimidin-4-on.
4. Förfarande enligt patentkrav 1, kannetecknat av att man framställer 2-amino-3,5-dihydro-7-(3-tienylmetyl)-4H-pyrro- 1o[3,2 -d]pyrimidin-4 -on. 35
5. Förfarande enligt patentkrav 1, kännetecknat av att man framställer 2-amino-3,5-dihydro-7-(2-furanylmetyl)-4H-pyrro-lo[3,2-d]pyrimidin-4-on.
FI914015A 1989-02-27 1991-08-26 Förfarande för framställning av farmaceutiskt aktiva 7-substituerade-2-amino-3,5-dihydro-4H-pyrrolo/3,2-d/pyrimidin-4-oner FI95259C (sv)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US31606389A 1989-02-27 1989-02-27
US31606389 1989-02-27
US9001021 1990-02-27
PCT/US1990/001021 WO1990010631A1 (en) 1989-02-27 1990-02-27 9-substituted-8-unsubstituted-9-deazaguanines

Publications (3)

Publication Number Publication Date
FI914015A0 FI914015A0 (sv) 1991-08-26
FI95259B true FI95259B (sv) 1995-09-29
FI95259C FI95259C (sv) 1996-01-10

Family

ID=23227309

Family Applications (1)

Application Number Title Priority Date Filing Date
FI914015A FI95259C (sv) 1989-02-27 1991-08-26 Förfarande för framställning av farmaceutiskt aktiva 7-substituerade-2-amino-3,5-dihydro-4H-pyrrolo/3,2-d/pyrimidin-4-oner

Country Status (15)

Country Link
US (2) US5565463A (sv)
EP (1) EP0460116B1 (sv)
JP (1) JP2760364B2 (sv)
KR (1) KR100208315B1 (sv)
AT (1) ATE157363T1 (sv)
AU (1) AU640649B2 (sv)
CA (1) CA2047216C (sv)
DE (1) DE69031337T2 (sv)
DK (1) DK0460116T3 (sv)
ES (1) ES2106732T3 (sv)
FI (1) FI95259C (sv)
HU (1) HU217870B (sv)
NO (1) NO180049C (sv)
RU (1) RU2093513C1 (sv)
WO (1) WO1990010631A1 (sv)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0500653A4 (en) * 1989-10-31 1995-08-23 Biocryst Inc Inhibitors of purine nucleoside phosphorylase
US5726311A (en) * 1989-11-29 1998-03-10 Biocryst Pharmaceuticals, Inc. 7-disubstituted-methyl-4-oxo-3H,5H-pyrrolo 3,2-d!pyrimidine and pharmaceutical uses and compositions containing the same
US5236926A (en) * 1992-02-03 1993-08-17 Warner-Lambert Company 9-substituted-8-halo or -8-hydroxy-9-deazaguanines as inhibitors or PNP for pharmaceutical compositions
AU6855594A (en) 1993-06-30 1995-01-24 Biocryst Pharmaceuticals, Inc. 9-deazahypoxanthines as pnp inhibitors
US5650511A (en) * 1995-12-12 1997-07-22 Biocryst Pharmaceuticals, Inc. Process for the preparation of 9-deazaguanine derivatives
AR012871A1 (es) * 1997-05-29 2000-11-22 Novartis Ag 2-amino-7-(2-hidroxietilo-1-sustituido)-3,5-dihidropirrolo (3,2-d)pirimidin -4-onas, composiones farmaceuticas y el uso de las mismas para la manufacturade un medicamento.
US6355244B1 (en) 1997-11-17 2002-03-12 University Of Kentucky Research Foundation Methods and compositions for the treatment of psoriasis
US6174888B1 (en) 1998-05-28 2001-01-16 Novartis Ag 2-amino-7-(1-substituted-2-hydroxyethyl)-3,5-dihydropyrrolo[3,2-D]pyrimidin-4-ones
US20110104186A1 (en) 2004-06-24 2011-05-05 Nicholas Valiante Small molecule immunopotentiators and assays for their detection
US7763257B2 (en) 2004-12-09 2010-07-27 Christina Juneau Compositions comprising transforming growth factor (TGF)-β1 and TGF-β2 in admixture of proteins obtained from dairy products
UA104579C2 (uk) 2007-12-10 2014-02-25 Байокрист Фармасьютикалз, Инк. Спосіб лікування раку кровотворної системи із застосуванням фородезину у комбінації з ритуксимабом
WO2014205194A1 (en) 2013-06-22 2014-12-24 Nitor Therapeutics Compositions and methods for potentiating immune response for the treatment of infectious diseases and cancer
WO2020186187A1 (en) 2019-03-13 2020-09-17 University Of Pittsburgh - Of The Commonwealth System Of Higher Education Methods for treating bladder and urethra dysfunction and disease
GB202218782D0 (en) 2022-12-13 2023-01-25 Mehrling Thomas Purine nucleoside phosphorylase inhibitor for metabolic syndrome

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL76546A (en) * 1984-10-12 1988-12-30 Warner Lambert Co 9-(heteroarylalkyl)-6-purine(thi)one derivatives,their preparation and pharmaceutical compositions containing them
US4772606A (en) * 1985-08-22 1988-09-20 Warner-Lambert Company Purine derivatives
IE60433B1 (en) * 1986-08-26 1994-07-13 Warner Lambert Co Novel 9-deazaguanines
US4923872A (en) * 1986-08-26 1990-05-08 Warner-Lambert Co. Analogues of pyrrolo[3,2d]pyrimidin-4-ones
CA1294960C (en) * 1986-10-24 1992-01-28 Thomas C. Malone 7-deazaguanines as immunomodulators
NO169490C (no) * 1988-03-24 1992-07-01 Takeda Chemical Industries Ltd Analogifremgangsmaate for fremstilling av terapeutisk aktive pyrrolopyrimidinderivater
DE58902899D1 (de) * 1988-12-14 1993-01-14 Ciba Geigy Ag 2',3'-dideoxypurinnucleosid/purinnucleosid-phosphorylase-inhibitor kombinationstherapie und zusammensetzungen dafuer.

Also Published As

Publication number Publication date
DK0460116T3 (da) 1998-03-30
DE69031337T2 (de) 1998-03-05
HUT58737A (en) 1992-03-30
CA2047216A1 (en) 1990-08-28
AU5524890A (en) 1990-10-09
JPH04503675A (ja) 1992-07-02
JP2760364B2 (ja) 1998-05-28
NO180049B (no) 1996-10-28
WO1990010631A1 (en) 1990-09-20
EP0460116A4 (en) 1992-05-13
DE69031337D1 (de) 1997-10-02
ES2106732T3 (es) 1997-11-16
EP0460116B1 (en) 1997-08-27
FI95259C (sv) 1996-01-10
NO913332L (no) 1991-08-26
EP0460116A1 (en) 1991-12-11
US5565463A (en) 1996-10-15
FI914015A0 (sv) 1991-08-26
HU217870B (hu) 2000-04-28
KR920701209A (ko) 1992-08-11
NO913332D0 (no) 1991-08-26
CA2047216C (en) 1999-03-30
US5721240A (en) 1998-02-24
AU640649B2 (en) 1993-09-02
ATE157363T1 (de) 1997-09-15
RU2093513C1 (ru) 1997-10-20
KR100208315B1 (ko) 1999-07-15
NO180049C (no) 1997-02-05

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GB Transfer or assigment of application

Owner name: BIOCRYST PHARMACEUTICALS, INC.

BB Publication of examined application