BR9506667A - Composto intermediário de cloro-pirimidina processo para a preparação do composto intermediário de cloro-pirimidina processo para a preparação de 2,5-diamino-4,6-dicloro-pirimidina processo para a preparação de 2,6-diamino-purinas e processo para a preparação de (1s,4s)-4-2-amino-6-(ciclo-propil-amino)-9h-purin-9-il¾-2-ciclo-penteno-1-metanol - Google Patents
Composto intermediário de cloro-pirimidina processo para a preparação do composto intermediário de cloro-pirimidina processo para a preparação de 2,5-diamino-4,6-dicloro-pirimidina processo para a preparação de 2,6-diamino-purinas e processo para a preparação de (1s,4s)-4-2-amino-6-(ciclo-propil-amino)-9h-purin-9-il¾-2-ciclo-penteno-1-metanolInfo
- Publication number
- BR9506667A BR9506667A BR9506667A BR9506667A BR9506667A BR 9506667 A BR9506667 A BR 9506667A BR 9506667 A BR9506667 A BR 9506667A BR 9506667 A BR9506667 A BR 9506667A BR 9506667 A BR9506667 A BR 9506667A
- Authority
- BR
- Brazil
- Prior art keywords
- preparation
- pyrimidine
- diamino
- cyclo
- amino
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 6
- QWBAOXACRYJBED-UHFFFAOYSA-N [Cl].C1=CN=CN=C1 Chemical compound [Cl].C1=CN=CN=C1 QWBAOXACRYJBED-UHFFFAOYSA-N 0.000 title 2
- 150000001875 compounds Chemical class 0.000 title 2
- ZXWGHENZKVQKPX-UHFFFAOYSA-N 4,6-dichloropyrimidine-2,5-diamine Chemical compound NC1=NC(Cl)=C(N)C(Cl)=N1 ZXWGHENZKVQKPX-UHFFFAOYSA-N 0.000 title 1
- MSSXOMSJDRHRMC-UHFFFAOYSA-N 9H-purine-2,6-diamine Chemical class NC1=NC(N)=C2NC=NC2=N1 MSSXOMSJDRHRMC-UHFFFAOYSA-N 0.000 title 1
- 125000006317 cyclopropyl amino group Chemical group 0.000 title 1
- -1 9-substituted-2-aminopurines Chemical class 0.000 abstract 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 238000013160 medical therapy Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/50—Three nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/40—Heterocyclic compounds containing purine ring systems with halogen atoms or perhalogeno-alkyl radicals directly attached in position 2 or 6
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Virology (AREA)
- Public Health (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Communicable Diseases (AREA)
- Veterinary Medicine (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Catalysts (AREA)
- Indole Compounds (AREA)
- Saccharide Compounds (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Liquid Crystal Substances (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9402161A GB9402161D0 (en) | 1994-02-04 | 1994-02-04 | Chloropyrimidine intermediates |
| PCT/GB1995/000225 WO1995021161A1 (en) | 1994-02-04 | 1995-02-03 | Chloropyrimide intermediates |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BR9506667A true BR9506667A (pt) | 1997-09-16 |
Family
ID=10749873
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BR9506667A BR9506667A (pt) | 1994-02-04 | 1995-02-03 | Composto intermediário de cloro-pirimidina processo para a preparação do composto intermediário de cloro-pirimidina processo para a preparação de 2,5-diamino-4,6-dicloro-pirimidina processo para a preparação de 2,6-diamino-purinas e processo para a preparação de (1s,4s)-4-2-amino-6-(ciclo-propil-amino)-9h-purin-9-il¾-2-ciclo-penteno-1-metanol |
Country Status (27)
| Country | Link |
|---|---|
| US (8) | US6448403B1 (pt) |
| EP (1) | EP0741710B1 (pt) |
| JP (1) | JP3670012B2 (pt) |
| KR (1) | KR100355983B1 (pt) |
| CN (2) | CN1105109C (pt) |
| AT (1) | ATE192742T1 (pt) |
| AU (1) | AU690203B2 (pt) |
| BR (1) | BR9506667A (pt) |
| DE (1) | DE69516847T2 (pt) |
| DK (1) | DK0741710T3 (pt) |
| ES (1) | ES2148486T3 (pt) |
| FI (1) | FI112477B (pt) |
| GB (1) | GB9402161D0 (pt) |
| GR (1) | GR3033850T3 (pt) |
| HU (1) | HU223096B1 (pt) |
| IL (1) | IL112539A (pt) |
| MX (1) | MX9603091A (pt) |
| MY (1) | MY113775A (pt) |
| NO (1) | NO310819B1 (pt) |
| NZ (1) | NZ278948A (pt) |
| PL (1) | PL183885B1 (pt) |
| PT (1) | PT741710E (pt) |
| RU (1) | RU2140913C1 (pt) |
| SG (1) | SG47918A1 (pt) |
| TW (1) | TW390877B (pt) |
| WO (1) | WO1995021161A1 (pt) |
| ZA (1) | ZA95884B (pt) |
Families Citing this family (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9402161D0 (en) * | 1994-02-04 | 1994-03-30 | Wellcome Found | Chloropyrimidine intermediates |
| CA2145928C (en) * | 1994-04-27 | 2007-10-09 | Gerhard Stucky | N-(2-amino-4,6-dichloropyrimidin-5-yl)formamide, and a process for its preparation |
| ZA9510482B (en) * | 1994-12-12 | 1996-09-17 | Smithkline Beecham Plc | Pharmaceuticals |
| SK285229B6 (sk) | 1997-05-13 | 2006-09-07 | Lonza Ag | Spôsob výroby derivátov (1R,4S)- alebo (1S,4R)-1-amino-4- (hydroxymetyl)-2-cyklopenténu a enantioméru (1R,4S)-N-butyryl-1- amino-4-(hydroxymetyl)-2-cyklopenténu |
| GB9721780D0 (en) * | 1997-10-14 | 1997-12-10 | Glaxo Group Ltd | Process for the synthesis of chloropurine intermediates |
| AU2702899A (en) * | 1997-10-24 | 1999-05-17 | Glaxo Group Limited | Process for preparing a chiral nucleoside analogue |
| EP1032573A1 (en) * | 1997-11-12 | 2000-09-06 | Glaxo Group Limited | Process for preparing a chiral nucleoside analogue |
| SK284594B6 (sk) * | 1997-11-27 | 2005-07-01 | Lonza Ag | Spôsob výroby derivátov aminoalkoholov a ich soli |
| DK1013647T3 (da) * | 1998-12-21 | 2003-03-10 | Lonza Ag | Fremgangsmåde til fremstilling af N-(amino-4,6-dihalogenpyrimidin)-formamider |
| CA2440809A1 (en) * | 2001-03-01 | 2002-09-12 | Conforma Therapeutics Corp. | Methods for treating genetically-defined proliferative disorders with hsp90 inhibitors |
| EP1440072A4 (en) * | 2001-10-30 | 2005-02-02 | Conforma Therapeutic Corp | PURINE ANALOGS HAVING HSP90 INHIBITORY ACTIVITY |
| US20070129334A1 (en) * | 2001-10-30 | 2007-06-07 | Conforma Therapeutics Corporation | Orally Active Purine-Based Inhibitors of Heat Shock Protein 90 |
| US6780635B2 (en) | 2001-12-27 | 2004-08-24 | Council Of Scientific And Industrial Research | Process for the preparation of optically active azabicyclo heptanone derivatives |
| KR100573859B1 (ko) * | 2002-07-15 | 2006-04-25 | 경동제약 주식회사 | 9-[4-아세톡시-3-(아세톡시메틸)부트-1-일]-2-아미노푸린의제조방법 |
| US7560231B2 (en) * | 2002-12-20 | 2009-07-14 | Roche Molecular Systems, Inc. | Mannitol and glucitol derivatives |
| WO2004099208A1 (en) * | 2003-04-30 | 2004-11-18 | Teva Pharmaceutical Industries Ltd. | Process for the preparation of famciclovir |
| JPWO2004103979A1 (ja) * | 2003-05-26 | 2006-07-20 | 住友化学株式会社 | N−(2−アミノ−4,6−ジクロロピリミジン−5−イル)ホルムアミドの製造方法 |
| KR100573860B1 (ko) * | 2003-06-13 | 2006-04-25 | 경동제약 주식회사 | 2-아미노-9-(2-치환에틸)푸린을 이용한 9-[4-아세톡시-3-(아세톡시메틸)부트-1-일]-2-아미노푸린의 제조방법 |
| US6930093B2 (en) * | 2003-07-10 | 2005-08-16 | Valeant Research & Development | Use of ribofuranose derivatives against inflammatory bowel diseases |
| KR100573861B1 (ko) * | 2003-07-18 | 2006-04-25 | 경동제약 주식회사 | 2-아미노-9-(2-할로게노에틸)푸린 및 그 중간체로서의 2-아미노-6,8-디클로로-9-(2-히드록시에틸)푸린의 제조방법 |
| US20050143400A1 (en) * | 2003-09-04 | 2005-06-30 | Genny Shamai | Process for preparing famciclovir |
| GB0320738D0 (en) | 2003-09-04 | 2003-10-08 | Glaxo Group Ltd | Novel process |
| BRPI0414533A (pt) * | 2003-09-18 | 2006-11-07 | Conforma Therapeutics Corp | composto, composição farmacêutica, e, métodos para inibir um hsp90 e para tratar um indivìduo tendo um distúrbio mediado por hsp90 |
| DE102004002055A1 (de) * | 2004-01-15 | 2005-08-11 | Degussa Ag | Verfahren zur Herstellung von 2-Amino-4,6-dichlor-5-formamidopyrimidin |
| EA012799B1 (ru) * | 2004-08-16 | 2009-12-30 | Кварк Фармасьютикалс, Инк. | Терапевтические применения ингибиторов rtp801 |
| WO2006105372A2 (en) | 2005-03-30 | 2006-10-05 | Conforma Therapeutics Corporation | Alkynyl pyrrolopyrimidines and related analogs as hsp90-inhibitors |
| GB2426247A (en) | 2005-05-20 | 2006-11-22 | Arrow Int Ltd | Methods of preparing purine derivatives such as famciclovir |
| WO2007035963A2 (en) * | 2005-09-23 | 2007-03-29 | Conforma Therapeutics Corporation | Anti-tumor methods using multi drug resistance independent synthetic hsp90 inhibitors |
| EP1857458A1 (en) * | 2006-05-05 | 2007-11-21 | SOLMAG S.p.A. | Process for the preparation of abacavir |
| CN100465174C (zh) * | 2006-06-13 | 2009-03-04 | 中国科学院上海有机化学研究所 | 制备光学纯阿巴卡韦的方法 |
| WO2008072074A1 (en) * | 2006-12-11 | 2008-06-19 | Aurobindo Pharma Limited | An improved process for the preparation of purine derivative |
| EP1939196A1 (en) | 2006-12-21 | 2008-07-02 | Esteve Quimica, S.A. | Process for the preparation of abacavir |
| EP2170840A1 (en) * | 2007-06-21 | 2010-04-07 | Aurobindo Pharma Ltd | An improved process for preparing purine derivative |
| EP2085397A1 (en) | 2008-01-21 | 2009-08-05 | Esteve Quimica, S.A. | Crystalline form of abacavir |
| SMT201800290T1 (it) | 2010-01-27 | 2018-07-17 | Viiv Healthcare Co | Terapia antivirale |
| CZ305457B6 (cs) | 2011-02-28 | 2015-09-30 | Ústav organické chemie a biochemie, Akademie věd ČR v. v. i. | Pyrimidinové sloučeniny inhibující tvorbu oxidu dusnatého a prostaglandinu E2, způsob výroby a použití |
| EP2962693B1 (en) | 2013-02-27 | 2019-01-09 | Kyoto University | Pharmaceutical composition comprising abacavir for the treatment of cancer |
| CN104672239A (zh) * | 2013-11-26 | 2015-06-03 | 上海迪赛诺化学制药有限公司 | 一种采用一锅法制备阿巴卡韦式v中间体的工艺 |
| CN109456329B (zh) * | 2018-11-19 | 2021-03-09 | 迪嘉药业集团有限公司 | 一种泛昔洛韦的制备方法 |
| CN113292507B (zh) * | 2021-06-25 | 2022-07-19 | 潍坊奥通药业有限公司 | 一种2-氨基-6-氯鸟嘌呤及其中间体的制备方法 |
| CN116239596A (zh) * | 2022-11-28 | 2023-06-09 | 安徽贝克制药股份有限公司 | 一种阿巴卡韦杂质a的制备方法及用途 |
| CN118852029B (zh) * | 2024-09-23 | 2025-02-07 | 苏州开元民生科技股份有限公司 | 一种制备2-氨基-4,6-二氯-5-甲酰胺基嘧啶的方法 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0141927B1 (en) | 1983-08-18 | 1991-10-30 | Beecham Group Plc | Antiviral guanine derivatives |
| DE3582399D1 (de) | 1984-09-20 | 1991-05-08 | Beecham Group Plc | Purin-derivate und ihre pharmazeutische verwendung. |
| MY101126A (en) * | 1985-12-13 | 1991-07-31 | Beecham Group Plc | Novel compounds |
| US4965270A (en) | 1987-05-30 | 1990-10-23 | Beecham Group P.L.C. | Purine derivatives |
| GB8724765D0 (en) | 1987-10-22 | 1987-11-25 | Beecham Group Plc | Process |
| US5631370A (en) | 1988-01-20 | 1997-05-20 | Regents Of The University Of Minnesota | Optically-active isomers of dideoxycarbocyclic nucleosides |
| GB2243609B (en) * | 1988-01-20 | 1992-03-11 | Univ Minnesota | Dideoxydidehydrocarbocyclic pyrimidines |
| US4916224A (en) | 1988-01-20 | 1990-04-10 | Regents Of The University Of Minnesota | Dideoxycarbocyclic nucleosides |
| GB8815265D0 (en) | 1988-06-27 | 1988-08-03 | Wellcome Found | Therapeutic nucleosides |
| GB8916698D0 (en) | 1989-07-21 | 1989-09-06 | Beecham Group Plc | Novel process |
| GB8918827D0 (en) | 1989-08-17 | 1989-09-27 | Beecham Group Plc | Novel compounds |
| MY104575A (en) | 1989-12-22 | 1994-04-30 | The Wellcome Foundation Ltd | Therapeutic nucleosides. |
| CZ287049B6 (cs) | 1992-01-22 | 2000-08-16 | Lonza A. G. | N-5-chráněné 2,5-diamino-4,6-dichlorpyrimidiny a způsob jejich přípravy |
| JPH05320143A (ja) * | 1992-03-18 | 1993-12-03 | Mochida Pharmaceut Co Ltd | 新規ピリミジン誘導体 |
| GB9402161D0 (en) * | 1994-02-04 | 1994-03-30 | Wellcome Found | Chloropyrimidine intermediates |
| CA2145928C (en) | 1994-04-27 | 2007-10-09 | Gerhard Stucky | N-(2-amino-4,6-dichloropyrimidin-5-yl)formamide, and a process for its preparation |
-
1994
- 1994-02-04 GB GB9402161A patent/GB9402161D0/en active Pending
-
1995
- 1995-02-03 IL IL11253995A patent/IL112539A/xx not_active IP Right Cessation
- 1995-02-03 EP EP95907107A patent/EP0741710B1/en not_active Expired - Lifetime
- 1995-02-03 NZ NZ278948A patent/NZ278948A/en not_active IP Right Cessation
- 1995-02-03 BR BR9506667A patent/BR9506667A/pt not_active IP Right Cessation
- 1995-02-03 AT AT95907107T patent/ATE192742T1/de active
- 1995-02-03 KR KR1019960704228A patent/KR100355983B1/ko not_active Expired - Lifetime
- 1995-02-03 ZA ZA95884A patent/ZA95884B/xx unknown
- 1995-02-03 HU HU9602114A patent/HU223096B1/hu active IP Right Grant
- 1995-02-03 WO PCT/GB1995/000225 patent/WO1995021161A1/en not_active Ceased
- 1995-02-03 PT PT95907107T patent/PT741710E/pt unknown
- 1995-02-03 DE DE69516847T patent/DE69516847T2/de not_active Expired - Lifetime
- 1995-02-03 PL PL95315713A patent/PL183885B1/pl unknown
- 1995-02-03 MY MYPI95000246A patent/MY113775A/en unknown
- 1995-02-03 DK DK95907107T patent/DK0741710T3/da active
- 1995-02-03 CN CN95191478A patent/CN1105109C/zh not_active Expired - Lifetime
- 1995-02-03 CN CNB021023441A patent/CN1161343C/zh not_active Expired - Lifetime
- 1995-02-03 RU RU96118435A patent/RU2140913C1/ru active
- 1995-02-03 US US08/682,743 patent/US6448403B1/en not_active Expired - Lifetime
- 1995-02-03 ES ES95907107T patent/ES2148486T3/es not_active Expired - Lifetime
- 1995-02-03 AU AU15438/95A patent/AU690203B2/en not_active Expired
- 1995-02-03 JP JP52046795A patent/JP3670012B2/ja not_active Expired - Lifetime
- 1995-02-03 SG SG1996005343A patent/SG47918A1/en unknown
- 1995-03-14 TW TW084102412A patent/TW390877B/zh not_active IP Right Cessation
-
1996
- 1996-07-30 MX MX9603091A patent/MX9603091A/es unknown
- 1996-08-02 NO NO19963239A patent/NO310819B1/no not_active IP Right Cessation
- 1996-08-02 FI FI963070A patent/FI112477B/fi not_active IP Right Cessation
-
1997
- 1997-10-24 US US08/957,603 patent/US6087501A/en not_active Expired - Lifetime
- 1997-10-24 US US08/957,606 patent/US6555687B1/en not_active Expired - Lifetime
- 1997-10-24 US US08/957,605 patent/US5917042A/en not_active Expired - Lifetime
- 1997-10-24 US US08/957,043 patent/US5917041A/en not_active Expired - Lifetime
-
1999
- 1999-10-15 US US09/419,416 patent/US6552193B1/en not_active Expired - Lifetime
-
2000
- 2000-06-30 GR GR20000401551T patent/GR3033850T3/el unknown
-
2002
- 2002-06-27 US US10/184,482 patent/US6870053B2/en not_active Expired - Fee Related
-
2003
- 2003-03-18 US US10/389,815 patent/US20030187263A1/en not_active Abandoned
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