DK0741710T3 - Chlorpyrimidin-mellemprodukter - Google Patents

Chlorpyrimidin-mellemprodukter

Info

Publication number
DK0741710T3
DK0741710T3 DK95907107T DK95907107T DK0741710T3 DK 0741710 T3 DK0741710 T3 DK 0741710T3 DK 95907107 T DK95907107 T DK 95907107T DK 95907107 T DK95907107 T DK 95907107T DK 0741710 T3 DK0741710 T3 DK 0741710T3
Authority
DK
Denmark
Prior art keywords
intermediates
processes
chloropyrimidine
chloropyrimidine intermediates
aminopurines
Prior art date
Application number
DK95907107T
Other languages
English (en)
Inventor
Susan Mary Daluge
Michael Tolar Martin
Michelle Joanne Ferry Fugett
Original Assignee
Wellcome Found
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=10749873&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=DK0741710(T3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Wellcome Found filed Critical Wellcome Found
Application granted granted Critical
Publication of DK0741710T3 publication Critical patent/DK0741710T3/da

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic 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
    • C07D239/28Heterocyclic 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
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/48Two nitrogen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic 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
    • C07D239/28Heterocyclic 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
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/50Three nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/40Heterocyclic compounds containing purine ring systems with halogen atoms or perhalogeno-alkyl radicals directly attached in position 2 or 6
DK95907107T 1994-02-04 1995-02-03 Chlorpyrimidin-mellemprodukter DK0741710T3 (da)

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
DK0741710T3 true DK0741710T3 (da) 2000-08-14

Family

ID=10749873

Family Applications (1)

Application Number Title Priority Date Filing Date
DK95907107T DK0741710T3 (da) 1994-02-04 1995-02-03 Chlorpyrimidin-mellemprodukter

Country Status (28)

Country Link
US (8) US6448403B1 (da)
EP (1) EP0741710B1 (da)
JP (1) JP3670012B2 (da)
KR (1) KR100355983B1 (da)
CN (2) CN1161343C (da)
AT (1) ATE192742T1 (da)
AU (1) AU690203B2 (da)
BR (1) BR9506667A (da)
DE (1) DE69516847T2 (da)
DK (1) DK0741710T3 (da)
ES (1) ES2148486T3 (da)
FI (1) FI112477B (da)
GB (1) GB9402161D0 (da)
GR (1) GR3033850T3 (da)
HK (1) HK1004087A1 (da)
HU (1) HU223096B1 (da)
IL (1) IL112539A (da)
MX (1) MX9603091A (da)
MY (1) MY113775A (da)
NO (1) NO310819B1 (da)
NZ (1) NZ278948A (da)
PL (1) PL183885B1 (da)
PT (1) PT741710E (da)
RU (1) RU2140913C1 (da)
SG (1) SG47918A1 (da)
TW (1) TW390877B (da)
WO (1) WO1995021161A1 (da)
ZA (1) ZA95884B (da)

Families Citing this family (39)

* Cited by examiner, † Cited by third party
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
SK284810B6 (sk) 1997-05-13 2005-12-01 Lonza Ag Spôsob výroby (1S,4R)- alebo (1R,4S)-4-(2-amino-6-chlór-9-H- purín-9-yl)-2-cyklopentén-1-metanolu
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
AU5653498A (en) * 1997-11-12 1999-05-31 Glaxo Group Limited Process for preparing a chiral nucleoside analogue
CZ298913B6 (cs) * 1997-11-27 2008-03-12 Lonza Ag Zpusob výroby aminoalkoholu a jeho derivátu
ATE228508T1 (de) * 1998-12-21 2002-12-15 Lonza Ag Verfahren zur herstellung von n-(amino-4,6- dihalogenpyrimidin)-formamiden
EP1423080A4 (en) * 2001-03-01 2009-06-03 Conforma Therapeutics Corp PROCESS FOR TREATING PROLIFERATIVE GENETIC 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
US7138402B2 (en) * 2003-09-18 2006-11-21 Conforma Therapeutics Corporation Pyrrolopyrimidines and related analogs as HSP90-inhibitors
US7560231B2 (en) * 2002-12-20 2009-07-14 Roche Molecular Systems, Inc. Mannitol and glucitol derivatives
US20040266795A1 (en) * 2003-04-30 2004-12-30 Genny Shamai Process for the preparation of famciclovir
WO2004103979A1 (ja) * 2003-05-26 2004-12-02 Sumitomo Chemical Company, Limited 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
GB0320738D0 (en) * 2003-09-04 2003-10-08 Glaxo Group Ltd Novel process
WO2005026167A1 (en) * 2003-09-04 2005-03-24 Teva Pharmaceutical Industries Ltd. Process for preparing famciclovir
DE102004002055A1 (de) * 2004-01-15 2005-08-11 Degussa Ag Verfahren zur Herstellung von 2-Amino-4,6-dichlor-5-formamidopyrimidin
AP2007003921A0 (en) * 2004-08-16 2007-02-28 Atugen Ag Therapeutic uses of inhibitors of rtp801
JP2008534609A (ja) * 2005-03-30 2008-08-28 コンフォーマ・セラピューティクス・コーポレイション Hsp90阻害剤としてのアルキニルピロロピリミジンおよび関連類似体
GB2426247A (en) 2005-05-20 2006-11-22 Arrow Int Ltd Methods of preparing purine derivatives such as famciclovir
US20070105874A1 (en) * 2005-09-23 2007-05-10 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
WO2008155613A1 (en) * 2007-06-21 2008-12-24 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
UA105556C2 (uk) 2010-01-27 2014-05-26 Віів Гелскер Компані Комбінація сполук, що містить інгібітори віл інтегрази з іншими терапевтичними агентами
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
WO2014133085A1 (ja) 2013-02-27 2014-09-04 国立大学法人京都大学 がんの予防または治療用医薬組成物
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

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3485225D1 (de) 1983-08-18 1991-12-05 Beecham Group Plc Antivirale guanin-derivate.
EP0182024B1 (en) 1984-09-20 1991-04-03 Beecham Group Plc Purine derivatives and their pharmaceutical use
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
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
US5631370A (en) 1988-01-20 1997-05-20 Regents Of The University Of Minnesota Optically-active isomers of 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.
SK279618B6 (sk) * 1992-01-22 1999-01-11 Lonza A.G. (Dir.:Basel) N-5-chránené 2,5-diamino-4,6-dichlórpyrimidíny a s
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

Also Published As

Publication number Publication date
ATE192742T1 (de) 2000-05-15
FI112477B (fi) 2003-12-15
CN1105109C (zh) 2003-04-09
PT741710E (pt) 2000-09-29
EP0741710B1 (en) 2000-05-10
KR100355983B1 (ko) 2002-12-28
JPH09508412A (ja) 1997-08-26
NO963239L (no) 1996-10-02
RU2140913C1 (ru) 1999-11-10
FI963070A0 (fi) 1996-08-02
BR9506667A (pt) 1997-09-16
CN1139924A (zh) 1997-01-08
GR3033850T3 (en) 2000-10-31
NZ278948A (en) 1998-01-26
SG47918A1 (en) 1998-04-17
IL112539A0 (en) 1995-05-26
WO1995021161A1 (en) 1995-08-10
MX9603091A (es) 1998-01-31
US6870053B2 (en) 2005-03-22
HUT75300A (en) 1997-05-28
US5917041A (en) 1999-06-29
NO310819B1 (no) 2001-09-03
AU1543895A (en) 1995-08-21
US6087501A (en) 2000-07-11
MY113775A (en) 2002-05-31
CN1161343C (zh) 2004-08-11
US6552193B1 (en) 2003-04-22
FI963070A (fi) 1996-08-02
US6555687B1 (en) 2003-04-29
HU9602114D0 (en) 1996-09-30
DE69516847D1 (de) 2000-06-15
US20030187263A1 (en) 2003-10-02
NO963239D0 (no) 1996-08-02
GB9402161D0 (en) 1994-03-30
IL112539A (en) 2000-08-31
JP3670012B2 (ja) 2005-07-13
HU223096B1 (hu) 2004-03-29
ZA95884B (en) 1996-08-05
DE69516847T2 (de) 2000-10-26
US6448403B1 (en) 2002-09-10
PL183885B1 (pl) 2002-07-31
PL315713A1 (en) 1996-11-25
TW390877B (en) 2000-05-21
EP0741710A1 (en) 1996-11-13
AU690203B2 (en) 1998-04-23
CN1388123A (zh) 2003-01-01
HK1004087A1 (en) 1998-11-13
US5917042A (en) 1999-06-29
ES2148486T3 (es) 2000-10-16
US20020173649A1 (en) 2002-11-21

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