WO2002060905A2 - Procede pour preparer des intermediaires d'inhibiteurs de la protease du vih - Google Patents
Procede pour preparer des intermediaires d'inhibiteurs de la protease du vih Download PDFInfo
- Publication number
- WO2002060905A2 WO2002060905A2 PCT/US2001/046116 US0146116W WO02060905A2 WO 2002060905 A2 WO2002060905 A2 WO 2002060905A2 US 0146116 W US0146116 W US 0146116W WO 02060905 A2 WO02060905 A2 WO 02060905A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- furan
- propynyloxy
- group
- 6alkyl
- hydrogen
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Enzymes And Modification Thereof (AREA)
Abstract
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US24282200P | 2000-10-24 | 2000-10-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2002060905A2 true WO2002060905A2 (fr) | 2002-08-08 |
Family
ID=22916319
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2001/046116 WO2002060905A2 (fr) | 2000-10-24 | 2001-10-22 | Procede pour preparer des intermediaires d'inhibiteurs de la protease du vih |
PCT/US2001/051428 WO2002067239A2 (fr) | 2000-10-24 | 2001-10-22 | Methode de preparation d'intermediaires d'inhibiteurs de protease vih |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2001/051428 WO2002067239A2 (fr) | 2000-10-24 | 2001-10-22 | Methode de preparation d'intermediaires d'inhibiteurs de protease vih |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP1404680A2 (fr) |
JP (1) | JP2004519473A (fr) |
AU (1) | AU2002255473A1 (fr) |
WO (2) | WO2002060905A2 (fr) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004002975A1 (fr) * | 2002-06-27 | 2004-01-08 | Smithkline Beecham Corporation | PREPARATION DE STEREOISOMERES DE (3ALPHA, 3ALPHA/BETA, 6ALPHA/BETA) HEXAHYDROFURO[2,3-b]FURAN-3-OL |
US8153829B2 (en) | 2006-11-09 | 2012-04-10 | Janssen Pharmaceutica N.V. | Methods for the preparation of hexahydrofuro[2,3-B]furan-3-ol |
CN102516259A (zh) * | 2006-03-29 | 2012-06-27 | 吉里德科学公司 | 制备hiv蛋白酶抑制剂的方法 |
CN103864813A (zh) * | 2012-12-18 | 2014-06-18 | 上海迪赛诺化学制药有限公司 | 一种合成六氢呋喃并[2,3-b]呋喃-3-醇及其对映体的方法 |
CN107607635A (zh) * | 2017-08-15 | 2018-01-19 | 东北制药集团股份有限公司 | 一种采用顶空气相色谱检测左磷右胺盐中丙炔醇含量的方法 |
US11827627B2 (en) | 2021-06-04 | 2023-11-28 | Vertex Pharmaceuticals Incorporated | N-(hydroxyalkyl (hetero)aryl) tetrahydrofuran carboxamides as modulators of sodium channels |
US11834441B2 (en) | 2019-12-06 | 2023-12-05 | Vertex Pharmaceuticals Incorporated | Substituted tetrahydrofurans as modulators of sodium channels |
-
2001
- 2001-10-22 AU AU2002255473A patent/AU2002255473A1/en not_active Abandoned
- 2001-10-22 WO PCT/US2001/046116 patent/WO2002060905A2/fr active Application Filing
- 2001-10-22 WO PCT/US2001/051428 patent/WO2002067239A2/fr not_active Application Discontinuation
- 2001-10-22 JP JP2002566479A patent/JP2004519473A/ja active Pending
- 2001-10-22 EP EP01271082A patent/EP1404680A2/fr not_active Withdrawn
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004002975A1 (fr) * | 2002-06-27 | 2004-01-08 | Smithkline Beecham Corporation | PREPARATION DE STEREOISOMERES DE (3ALPHA, 3ALPHA/BETA, 6ALPHA/BETA) HEXAHYDROFURO[2,3-b]FURAN-3-OL |
CN102516259A (zh) * | 2006-03-29 | 2012-06-27 | 吉里德科学公司 | 制备hiv蛋白酶抑制剂的方法 |
CN102516259B (zh) * | 2006-03-29 | 2014-12-10 | 吉里德科学公司 | 制备hiv蛋白酶抑制剂的方法 |
US8153829B2 (en) | 2006-11-09 | 2012-04-10 | Janssen Pharmaceutica N.V. | Methods for the preparation of hexahydrofuro[2,3-B]furan-3-ol |
CN103864813A (zh) * | 2012-12-18 | 2014-06-18 | 上海迪赛诺化学制药有限公司 | 一种合成六氢呋喃并[2,3-b]呋喃-3-醇及其对映体的方法 |
CN107607635A (zh) * | 2017-08-15 | 2018-01-19 | 东北制药集团股份有限公司 | 一种采用顶空气相色谱检测左磷右胺盐中丙炔醇含量的方法 |
CN107607635B (zh) * | 2017-08-15 | 2020-07-31 | 东北制药集团股份有限公司 | 一种采用顶空气相色谱检测左磷右胺盐中丙炔醇含量的方法 |
US11834441B2 (en) | 2019-12-06 | 2023-12-05 | Vertex Pharmaceuticals Incorporated | Substituted tetrahydrofurans as modulators of sodium channels |
US11919887B2 (en) | 2019-12-06 | 2024-03-05 | Vertex Pharmaceuticals Incorporated | Substituted tetrahydrofurans as modulators of sodium channels |
US11827627B2 (en) | 2021-06-04 | 2023-11-28 | Vertex Pharmaceuticals Incorporated | N-(hydroxyalkyl (hetero)aryl) tetrahydrofuran carboxamides as modulators of sodium channels |
Also Published As
Publication number | Publication date |
---|---|
JP2004519473A (ja) | 2004-07-02 |
EP1404680A2 (fr) | 2004-04-07 |
WO2002067239A2 (fr) | 2002-08-29 |
AU2002255473A1 (en) | 2002-09-04 |
WO2002067239A3 (fr) | 2004-01-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6889232B2 (ja) | ハリコンドリンbの類縁体の合成において有用な大環化反応および中間体 | |
Ihara et al. | Asymmetric total synthesis of atisine via intramolecular double Michael reaction | |
Martin et al. | Application of nitrile oxide cycloadditions to a convergent, asymmetric synthesis of (+)-phyllanthocin | |
CN109641917A (zh) | 可用于合成软海绵素大环内酯类及其类似物的普林斯反应和中间体 | |
Majumdar et al. | Synthesis of five-and six-membered heterocyclic compounds by the application of the metathesis reactions | |
Li et al. | Phosphine-containing Lewis base catalyzed cyclization of benzofuranone type electron-deficient alkenes with allenoates: a facile synthesis of spirocyclic benzofuranones | |
WO2002060905A2 (fr) | Procede pour preparer des intermediaires d'inhibiteurs de la protease du vih | |
Finch et al. | Synthesis of the spiroacetal core of the cephalosporolide family of natural products | |
Yan et al. | Synthesis of bicyclic ortho-aminocarbonitrile derivatives catalyzed by 1, 4-diazabicyclo [2.2. 2] octane | |
KR900005624B1 (ko) | 에피포도필로톡신과 그 관련화합물 제조용 중간화합물 및 그 제조방법 | |
US7145024B2 (en) | Process for preparing protease inhibitor intermediates | |
US20040026230A1 (en) | Process for preparing intermediates of hiv protease inhibitors | |
Toyooka et al. | Stereodivergent synthesis of the 2, 3, 5, 6-tetrasubstituted piperidine ring system: An application to the synthesis of alkaloids 223A and 205B from poison frogs | |
Zhang et al. | Structure‐Unit‐Based Total Synthesis of (−)‐Sinulochmodin C | |
Palange et al. | TiCl 4-n-Bu 3 N-mediated cascade annulation of ketones with α-ketoesters: a facile synthesis of highly substituted fused γ-alkylidene-butenolides | |
Maezaki et al. | 1, 5-Benzodithiepan-3-one 1, 5-dioxide: A novel chiral auxiliary for asymmetric desymmetrization of meso-1, 2-diols | |
AU2002352205A1 (en) | Preparation of cis-fused 3,3a,8,12b-tetrahydro-2H-dibenzo[3,4:6,7]cyclohepta[1,2-b]furan derivatives | |
AU2002342926A1 (en) | Preparation of trans-fused 3,3a,8,12b-tetrahydro-2H-dibenzo[3,4:6,7]cyclohepta[1,2-b]furan derivatives | |
Harada et al. | Synthesis, absolute stereochemistry, and circular dichroism of chiral 1, 8a-dihydroazulene derivatives | |
Momose et al. | Bicyclo [3.3. 1] nonanes as synthetic intermediates. Part21. 1 Enantiodivergent synthesis of thecis, cis 2, 6-disubstituted piperidin-3-ol chiralbuilding block for alkaloid synthesis | |
Kraus et al. | A direct synthesis of hydroxysemperoside deglucoside | |
Honda et al. | An enantiocontrolled synthesis of (–)-malyngolide | |
Cecchet et al. | Synthesis and Diels-Alder reactions of enantiopure (−)-trans-benzo [d]-dithiine-S, S'-dioxide | |
Kobayashi et al. | Total Synthesis of Lissoclinolide by Acid-Induced Lactonization of an (E)-α-Bromo-γ, δ-Epoxy Acrylate Derivative | |
Mouriès et al. | Stereoselective Conversion of Aucubin into Polyfunctionalized Tetrahydro‐1H‐cyclopenta [c] furan Glucosides |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A2 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ PH PL PT RO RU SD SE SG SI SK SL TJ TM TR TT TZ UA UG US UZ VN YU ZA ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A2 Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
REG | Reference to national code |
Ref country code: DE Ref legal event code: 8642 |
|
122 | Ep: pct application non-entry in european phase | ||
XX | Miscellaneous: |
Free format text: THE RECEIVING OFFICE HAS INFORMED THE IB THAT THIS INTERNATIONAL APPLICATION HAS BEEN ERRONEOUSLY ASSIGNED AN INTERENATIONAL FILING DATE AND IS VACATED AND REPLACED BY INTERNATIONAL APPLICATION PCT/US2001/051428. THE NOTICE WAS RECEIVED BY THE INTERNATIONAL BUREAU IN TIME TO PREVENT THE INTERNATIONAL PUBLICATION, HOWEVER, DUE TO A CLERICAL ERROR, THE APPLICATION PCT/US2001/046116 WAS NEVERTHELESS PUBLISHED ON 20020808 (THIS APPLICATION WAS PUBLISHED ON 20020829). |
|
NENP | Non-entry into the national phase |
Ref country code: JP |