EA200000859A1 - Способ синтеза ингибиторов протеазы вич - Google Patents

Способ синтеза ингибиторов протеазы вич

Info

Publication number
EA200000859A1
EA200000859A1 EA200000859A EA200000859A EA200000859A1 EA 200000859 A1 EA200000859 A1 EA 200000859A1 EA 200000859 A EA200000859 A EA 200000859A EA 200000859 A EA200000859 A EA 200000859A EA 200000859 A1 EA200000859 A1 EA 200000859A1
Authority
EA
Eurasian Patent Office
Prior art keywords
synthesis
protease inhibitors
hiv protease
isobutylbenzenesulfonamido
tetrahydro
Prior art date
Application number
EA200000859A
Other languages
English (en)
Other versions
EA003022B1 (ru
Inventor
Эмил Эл-Фархан
Дейвид Д. Дейнинджер
Стивен Макги
Джон О'Каллахан
Марк Стюарт Робертсон
Кейт Роджерс
Стивен Джон Рут
Хардев Сингх
Роджер Деннис Танг
Original Assignee
Глаксо Груп Лимитед
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 Глаксо Груп Лимитед filed Critical Глаксо Груп Лимитед
Publication of EA200000859A1 publication Critical patent/EA200000859A1/ru
Publication of EA003022B1 publication Critical patent/EA003022B1/ru

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D307/18—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D307/20—Oxygen 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
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/18—Antivirals for RNA viruses for HIV
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Abstract

Описан усовершенствованный способ синтеза (3S)-тетрагидро-3-фурилового эфира N-[(1S,2R)-3-(4-амино-N-изобутилбензолсульфонамидо)-1-бензил-2-гидроксипропил]карбаминовой кислоты, который включает в себя четыре стадии, из соединения формулы (A) и, кроме того, новое промежуточное соединение.Международная заявка была опубликована вместе с отчетом о международном поиске.
EA200000859A 1998-03-20 1999-03-18 Способ синтеза ингибиторов протеазы вич EA003022B1 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9805898.5A GB9805898D0 (en) 1998-03-20 1998-03-20 Process for the sythesis of hiv protease inhibitors
PCT/GB1999/000852 WO1999048885A1 (en) 1998-03-20 1999-03-18 Process for the synthesis of hiv protease inhibitors

Publications (2)

Publication Number Publication Date
EA200000859A1 true EA200000859A1 (ru) 2001-04-23
EA003022B1 EA003022B1 (ru) 2002-12-26

Family

ID=10828884

Family Applications (1)

Application Number Title Priority Date Filing Date
EA200000859A EA003022B1 (ru) 1998-03-20 1999-03-18 Способ синтеза ингибиторов протеазы вич

Country Status (32)

Country Link
US (1) US6281367B1 (ru)
EP (1) EP1066276B1 (ru)
JP (1) JP3363439B2 (ru)
KR (1) KR100555278B1 (ru)
CN (1) CN1308319C (ru)
AP (1) AP1226A (ru)
AT (1) ATE242772T1 (ru)
AU (1) AU751534B2 (ru)
BR (1) BR9908970A (ru)
CA (1) CA2324217C (ru)
CZ (1) CZ299193B6 (ru)
DE (1) DE69908761T2 (ru)
DK (1) DK1066276T3 (ru)
EA (1) EA003022B1 (ru)
EE (1) EE04750B1 (ru)
ES (1) ES2203090T3 (ru)
GB (1) GB9805898D0 (ru)
HK (1) HK1032047A1 (ru)
HR (1) HRP20000609B1 (ru)
HU (1) HUP0105439A3 (ru)
ID (1) ID26587A (ru)
IL (1) IL138127A (ru)
IS (1) IS2273B (ru)
NO (1) NO317648B1 (ru)
NZ (1) NZ506563A (ru)
PL (1) PL201810B1 (ru)
PT (1) PT1066276E (ru)
RS (1) RS49954B (ru)
SK (1) SK283939B6 (ru)
TR (1) TR200002698T2 (ru)
WO (1) WO1999048885A1 (ru)
ZA (1) ZA200004482B (ru)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5843946A (en) 1992-08-25 1998-12-01 G.D. Searle & Co. α-and β-amino acid hydroxyethylamino sulfonamides useful as retroviral protease inhibitors
US6548706B2 (en) * 1999-12-23 2003-04-15 Aerojet Fine Chemicals Llc Preparation of 2S,3S-N-isobutyl-N-(2-hydroxy-3-amino-4-phenylbutyl) -p-nitrobenzenesulfonylamide hydrochloride and other derivatives of 2-hydroxy-1,3-diamines
EP2314564A3 (en) * 1999-12-23 2012-04-04 Ampac Fine Chemicals LLC Improved preparation of 2S,3S-N-isobutyl-N-(2-hydroxy-3-amino-4-phenylbutyl)-p-nitrobenzenesulfonylamide hydrochloride and other derivatives of 2-hydroxy-1,3-diamines
HUE034389T2 (en) 2002-05-16 2018-02-28 Janssen Sciences Ireland Uc Pseudopolymorphic forms of an HIV protease inhibitor
US7772411B2 (en) 2003-12-23 2010-08-10 Tibotec Pharmaceuticals Ltd. Process for the preparation of (3R,3aS,6aR)-hexahydrofuro [2,3-b] furan-3-yl (1S,2R)-3[[(4-aminophenyl) sulfonyl] (isobutyl) amino]-1-benzyl-2-hydroxypropylcarbamate
AR073248A1 (es) 2008-09-01 2010-10-20 Tibotec Pharm Ltd Proceso para la preparacion de (1s, 2r)-3- ((4-aminofenil) sulfonil) ( isobutil) amino)-1- bencil-2- hidroxipropilcarbamato de (3r, 3as,6ar)- hexahidrofuro-(2,3-b) furan-3- ilo (darunavir) y compuestos intermediarios utiles en dicho proceso.
AP3551A (en) 2010-01-27 2016-01-18 Viiv Healthcare Co Antiviral therapy
WO2012032389A2 (en) 2010-09-10 2012-03-15 Lupin Limited Process for preparation of substantially pure fosamprenavir calcium and its intermediates
CN111233794A (zh) * 2020-03-27 2020-06-05 江巨东 一种安普那韦的精制方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1071930A (zh) * 1991-07-10 1993-05-12 伊莱利利公司 用作治疗艾滋病的人免疫缺陷病毒蛋白酶的抑制剂
US5843946A (en) * 1992-08-25 1998-12-01 G.D. Searle & Co. α-and β-amino acid hydroxyethylamino sulfonamides useful as retroviral protease inhibitors
US5723490A (en) * 1992-09-08 1998-03-03 Vertex Pharmaceuticals Incorporated THF-containing sulfonamide inhibitors of aspartyl protease
IS2334B (is) * 1992-09-08 2008-02-15 Vertex Pharmaceuticals Inc., (A Massachusetts Corporation) Aspartyl próteasi hemjari af nýjum flokki súlfonamíða

Also Published As

Publication number Publication date
EP1066276A1 (en) 2001-01-10
IS2273B (is) 2007-07-15
CA2324217A1 (en) 1999-09-30
ZA200004482B (en) 2001-11-28
CN1308319C (zh) 2007-04-04
CZ299193B6 (cs) 2008-05-14
EA003022B1 (ru) 2002-12-26
YU55900A (sh) 2003-02-28
HUP0105439A2 (en) 2002-06-29
IS5605A (is) 2000-08-29
CZ20003457A3 (cs) 2001-04-11
CN1293668A (zh) 2001-05-02
WO1999048885A1 (en) 1999-09-30
EP1066276B1 (en) 2003-06-11
GB9805898D0 (en) 1998-05-13
HRP20000609A2 (en) 2001-04-30
AP1226A (en) 2003-11-21
CA2324217C (en) 2008-02-19
AP2000001911A0 (en) 2000-09-30
KR100555278B1 (ko) 2006-03-03
RS49954B (sr) 2008-09-29
NO20004664L (no) 2000-09-19
SK283939B6 (sk) 2004-05-04
US6281367B1 (en) 2001-08-28
KR20010042022A (ko) 2001-05-25
ATE242772T1 (de) 2003-06-15
TR200002698T2 (tr) 2000-12-21
HK1032047A1 (en) 2001-07-06
NO317648B1 (no) 2004-11-29
HUP0105439A3 (en) 2002-08-28
IL138127A0 (en) 2001-10-31
AU2947599A (en) 1999-10-18
ID26587A (id) 2001-01-18
DK1066276T3 (da) 2003-10-06
DE69908761T2 (de) 2004-02-19
AU751534B2 (en) 2002-08-22
JP3363439B2 (ja) 2003-01-08
EE04750B1 (et) 2006-12-15
PL201810B1 (pl) 2009-05-29
EE200000568A (et) 2002-02-15
JP2002507609A (ja) 2002-03-12
DE69908761D1 (de) 2003-07-17
NZ506563A (en) 2003-05-30
PT1066276E (pt) 2003-10-31
PL342602A1 (en) 2001-06-18
IL138127A (en) 2003-10-31
NO20004664D0 (no) 2000-09-19
HRP20000609B1 (en) 2006-05-31
ES2203090T3 (es) 2004-04-01
SK13732000A3 (sk) 2001-08-06
BR9908970A (pt) 2000-11-28

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