WO1991018866A3 - 1,4-diamino-2,3-dihydroxybutanes - Google Patents
1,4-diamino-2,3-dihydroxybutanes Download PDFInfo
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- WO1991018866A3 WO1991018866A3 PCT/US1991/003852 US9103852W WO9118866A3 WO 1991018866 A3 WO1991018866 A3 WO 1991018866A3 US 9103852 W US9103852 W US 9103852W WO 9118866 A3 WO9118866 A3 WO 9118866A3
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- dihydroxybutanes
- diamino
- diamine
- preparing
- compounds
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- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/08—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
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- C07C215/22—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated
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- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
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- C07C2603/02—Ortho- or ortho- and peri-condensed systems
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- C07C2603/12—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings only one five-membered ring
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/56—Ring systems containing bridged rings
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- C07C2603/70—Ring systems containing bridged rings containing three rings containing only six-membered rings
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Abstract
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU82054/91A AU8205491A (en) | 1990-06-01 | 1991-05-31 | 1,4-diamino-2,3-dihydroxybutanes |
JP3512068A JPH07502970A (ja) | 1990-06-01 | 1991-05-31 | 1,4―ジアミノ―2,3―ジヒドロキシブタン類 |
BR919106540A BR9106540A (pt) | 1990-06-01 | 1991-05-31 | 1,4-diamino-2,3-didroxibutanos |
NO92924615A NO924615L (no) | 1990-06-01 | 1992-11-30 | 1,4-diamino-2,3-dihydroksybutaner |
FI925441A FI925441A0 (fi) | 1990-06-01 | 1992-11-30 | 1,4-diamino-2,3-dihydroxibutaner |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US53197190A | 1990-06-01 | 1990-06-01 | |
US531,971 | 1990-06-01 |
Publications (2)
Publication Number | Publication Date |
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WO1991018866A2 WO1991018866A2 (fr) | 1991-12-12 |
WO1991018866A3 true WO1991018866A3 (fr) | 1992-04-30 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1991/003852 WO1991018866A2 (fr) | 1990-06-01 | 1991-05-31 | 1,4-diamino-2,3-dihydroxybutanes |
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US (1) | US5294720A (fr) |
EP (2) | EP0532693A1 (fr) |
JP (1) | JPH07502970A (fr) |
BR (1) | BR9106540A (fr) |
CA (1) | CA2084087A1 (fr) |
HU (2) | HU9203505D0 (fr) |
TW (1) | TW204336B (fr) |
WO (1) | WO1991018866A2 (fr) |
ZA (1) | ZA914194B (fr) |
Families Citing this family (43)
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US6878728B1 (en) | 1999-06-11 | 2005-04-12 | Vertex Pharmaceutical Incorporated | Inhibitors of aspartyl protease |
US20040122000A1 (en) | 1981-01-07 | 2004-06-24 | Vertex Pharmaceuticals Incorporated. | Inhibitors of aspartyl protease |
US5552558A (en) * | 1989-05-23 | 1996-09-03 | Abbott Laboratories | Retroviral protease inhibiting compounds |
US5362912A (en) * | 1989-05-23 | 1994-11-08 | Abbott Laboratories | Process for the preparation of a substituted diaminodiol |
US5354866A (en) * | 1989-05-23 | 1994-10-11 | Abbott Laboratories | Retroviral protease inhibiting compounds |
EP0428849A3 (en) * | 1989-09-28 | 1991-07-31 | Hoechst Aktiengesellschaft | Retroviral protease inhibitors |
JPH06501681A (ja) * | 1990-07-06 | 1994-02-24 | スミスクライン・ビーチャム・コーポレイション | レトロウイルス・プロテアーゼの阻害剤 |
EP0503561B1 (fr) * | 1991-03-15 | 1998-10-28 | Hoechst Aktiengesellschaft | Procédé pour l'accouplement diastereoselective reductif des alpha aminoaldehydes homochirales |
US5430155A (en) * | 1991-05-31 | 1995-07-04 | The Du Pont Merck Pharmaceutical Company | 1,4-diamine-2,3-dihydroxy butanes |
EP0534511A1 (fr) * | 1991-08-16 | 1993-03-31 | Merck & Co. Inc. | Inhibiteurs de protéase de HIV utiles pour le traitement du SIDA |
US5491149A (en) * | 1991-09-16 | 1996-02-13 | The Du Pont Merck Pharmaceutical Company | Dihydroxypropylamine containing retroviral protease inhibitors |
DE59206778D1 (de) * | 1991-10-07 | 1996-08-22 | Hoechst Ag | Verfahren zur diastereoselektiven reduktiven Pinakol-Kupplung von homochiralen alpha-Aminoaldehyden |
US5610294A (en) * | 1991-10-11 | 1997-03-11 | The Du Pont Merck Pharmaceutical Company | Substituted cyclic carbonyls and derivatives thereof useful as retroviral protease inhibitors |
US6071895A (en) * | 1992-03-11 | 2000-06-06 | Narhex Limited | Polar-substituted hydrocarbons |
US5888992A (en) * | 1992-03-11 | 1999-03-30 | Narhex Limited | Polar substituted hydrocarbons |
MXPA93002392A (es) | 1992-03-11 | 2005-02-04 | Narhex Ltd | Derivados amino de hidrocarburos-oxo e hidroxi-substituidos. |
US5679688A (en) * | 1992-03-11 | 1997-10-21 | Narhex Limited | Quinaldoyl-amine derivatives of oxo-and hydroxy-substituted hydrocarbons |
US5559256A (en) * | 1992-07-20 | 1996-09-24 | E. R. Squibb & Sons, Inc. | Aminediol 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 |
US5783701A (en) * | 1992-09-08 | 1998-07-21 | Vertex Pharmaceuticals, Incorporated | Sulfonamide inhibitors of aspartyl protease |
DK0727419T3 (da) | 1992-12-29 | 2002-06-10 | Abbott Lab | Mellemprodukter til fremstilling af forbindelser, som inhiberer retroviral protease |
JP2787539B2 (ja) * | 1993-02-26 | 1998-08-20 | 松森 昭 | ウイルス性疾患の予防または治療剤 |
IL110898A0 (en) * | 1993-09-10 | 1994-11-28 | Narhex Australia Pty Ltd | Polar-substituted hydrocarbons |
US5559252A (en) * | 1994-02-16 | 1996-09-24 | The Dupont Merck Pharmaceutical Company | Process for the preparation of diamine intermediates useful in the synthesis of HIV protease inhibitors |
DE69512220T2 (de) * | 1994-03-07 | 2000-03-16 | Vertex Pharmaceuticals Inc. | Sulfonamidderivate als aspartylprotease-inhibitoren |
US5530124A (en) * | 1994-06-30 | 1996-06-25 | The Dupont Merck Pharmaceutical Company | Method for preparing cyclic ureas and their use for the synthesis of HIV protease inhibitors |
US5728718A (en) * | 1994-12-20 | 1998-03-17 | The United States Of America As Represented By The Department Of Health And Human Services | 2,5-diamino-3,4-disubstituted-1,6-diphenylhexane isosteres comprising benzamide, sulfonamide and anthranilamide subunits and methods of using same |
US5691368A (en) * | 1995-01-11 | 1997-11-25 | Hoechst Marion Roussel, Inc. | Substituted oxazolidine calpain and/or cathepsin B inhibitors |
US5691372A (en) * | 1995-04-19 | 1997-11-25 | Vertex Pharmaceuticals Incorporated | Oxygenated-Heterocycle containing sulfonamide inhibitors of aspartyl protease |
US6004957A (en) * | 1995-06-07 | 1999-12-21 | Vertex Pharmaceuticals, Incorporated | Sulfonamide inhibitors of aspartyl protease |
US5763464A (en) * | 1995-11-22 | 1998-06-09 | The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | Retroviral agents containing anthranilamide, substituted benzamide and other subunits, and methods of using same |
WO1998000173A2 (fr) * | 1996-07-03 | 1998-01-08 | Pharmacia & Upjohn Company | Distribution ciblee de medicaments a l'aide de derives de sulfonamides |
US6803466B1 (en) * | 1997-12-08 | 2004-10-12 | The Scripps Research Institute | HIV/FIV protease inhibitors having a small P3 residue |
US6436989B1 (en) | 1997-12-24 | 2002-08-20 | Vertex Pharmaceuticals, Incorporated | Prodrugs of aspartyl protease inhibitors |
JP4626896B2 (ja) | 1998-02-13 | 2011-02-09 | ダイセル化学工業株式会社 | アシル化剤とそれを用いたアシル化法、及びアダマンタン誘導体 |
DK1086076T3 (da) | 1998-06-19 | 2005-03-29 | Vertex Pharma | Sulfonamidinhibitorer af aspartylprotease |
US20050221457A1 (en) * | 2002-03-25 | 2005-10-06 | Paraskevas Tsobanakis | Methods of manufacturing derivatives of beta-hydroxycarboxylic acids |
US7834043B2 (en) * | 2003-12-11 | 2010-11-16 | Abbott Laboratories | HIV protease inhibiting compounds |
US20050131017A1 (en) | 2003-12-11 | 2005-06-16 | Degoey David A. | HIV protease inhibiting compounds |
AU2005323435A1 (en) * | 2004-05-04 | 2006-07-13 | Academia Sinica | Anti-coronavirus compounds |
WO2015058118A1 (fr) | 2013-10-17 | 2015-04-23 | Cargill, Incorporated | Procédé de production d'hydroxyalcanoates d'alkyle |
US10239819B2 (en) | 2014-10-17 | 2019-03-26 | Cargill, Incorporated | Methods for producing an ester of an alpha, beta-unsaturated carboxylic acid |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0361341A2 (fr) * | 1988-09-28 | 1990-04-04 | Miles Inc. | Agents thérapeutiques contre le SIDA basés sur des inhibiteurs des protéases du HIV |
EP0402646A1 (fr) * | 1989-05-23 | 1990-12-19 | Abbott Laboratories | Composés inhibiteurs de la protease retrovirale |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5151438A (en) * | 1989-05-23 | 1992-09-29 | Abbott Laboratories | Retroviral protease inhibiting compounds |
EP0428849A3 (en) * | 1989-09-28 | 1991-07-31 | Hoechst Aktiengesellschaft | Retroviral protease inhibitors |
-
1991
- 1991-05-31 EP EP91912877A patent/EP0532693A1/fr not_active Withdrawn
- 1991-05-31 HU HU9203505A patent/HU9203505D0/hu unknown
- 1991-05-31 WO PCT/US1991/003852 patent/WO1991018866A2/fr not_active Application Discontinuation
- 1991-05-31 JP JP3512068A patent/JPH07502970A/ja active Pending
- 1991-05-31 CA CA002084087A patent/CA2084087A1/fr not_active Abandoned
- 1991-05-31 US US07/714,042 patent/US5294720A/en not_active Expired - Fee Related
- 1991-05-31 BR BR919106540A patent/BR9106540A/pt not_active Application Discontinuation
- 1991-05-31 HU HU9203505A patent/HUT64738A/hu unknown
- 1991-05-31 EP EP95101007A patent/EP0665215A1/fr not_active Withdrawn
- 1991-06-03 ZA ZA914194A patent/ZA914194B/xx unknown
- 1991-08-17 TW TW080106534A patent/TW204336B/zh active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0361341A2 (fr) * | 1988-09-28 | 1990-04-04 | Miles Inc. | Agents thérapeutiques contre le SIDA basés sur des inhibiteurs des protéases du HIV |
EP0402646A1 (fr) * | 1989-05-23 | 1990-12-19 | Abbott Laboratories | Composés inhibiteurs de la protease retrovirale |
Non-Patent Citations (15)
Title |
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Bioorganic & Medicinal Chemistry Letters, vol. 1, no. 4, 1991, Pergamon Press (GB) B. Chenera et al.: "Synthesis of C2-symmetric and pseudosymmetric HIV-1 protease inhibitors from D-mannitol and D-arabitol", pages 219 - 222 * |
Carbohydrate Research, vol. 142, no. 1, 1 October 1985, Elsevir (NL) J. Kuszmann et al.: "Synthesis of 1,4:5-dianhydro-octitol derivatives", pages 61 - 69 * |
Carbohydrate Research, vol. 142, no. 1, 1 October 1985, Elsevir (NL) J. Kuszmann et al.: "Synthesis of 1,4:5-dianhydro-octitol derivatives", pages 61-69, see page 63, compounds nos. 13-19 * |
Journal of Medicinal Chemistry, vol. 33, no. 10, October 1990, Amercian Chemical Soc. (US), D.J. Kempf et al.: "Structure-based, C2 symmetric inhibitors of HIV protease", pages 2687 - 2689 * |
Tetrahedron Letters, no. 29, July 1975, Pergamon Press, L. Ötvös et al.: "Stereochemistry of the reactons of biopolymers III. Steric hindrance in the reactions of DNA with bifunctional alkylating agents", pages 2477 - 2481 * |
Tetrahedron Letters, no. 29, July 1975, Pergamon Press, L. Ötvös et al.: "Stereochemistry of the reactons of biopolymers III. Steric hindrance in the reactions of DNA with bifunctional alkylating agents", pages 2477-2481, see page 2478, figure III * |
Tetrahedron Letters, vol. 27, no. 35, 1986, Pergamon Press (GB), A. Duréault et al.: "Diastereospecific synthesis of diaziridines from D-mannitol. Access to chiral alpha-aminoacids", pages 4157 - 4160 * |
Tetrahedron Letters, vol. 28, no. 26, 1987, Pergamon Presss (GB) B. Achmatowicz et al.: "Transformations of tartaric acid. A facile synthesis of derivatives of optically active alpha-hydroxyaldehydes", pages 2999 - 3003 * |
Tetrahedron Letters, vol. 28, no. 26, 1987, Pergamon Presss (GB) B. Achmatowicz et al.: "Transformations of tartaric acid. A facile synthesis of derivatives of optically active alpha-hydroxyaldehydes", pages 2999-3003, see page 3001, compound nos. 6a,7,8 * |
Tetrahedron, vol. 45, no. 23, 1989, Pergamon Press (GB), M. Saniere et al.: "Syntheses of enantiomerically pure 9(S)- and 9(R)-hete from D-mannitol. Use of a malic dialdehyde equivalent", pages 7317 - 7328 * |
Tetrahedron, vol. 45, no. 23, 1989, Pergamon Press (GB), M. Saniere et al.: "Syntheses of enantiomerically pure 9(S)- and 9(R)-hete from D-mannitol. Use of a malic dialdehyde equivalent", pages 7317-7328, see page 7319, scheme I, page 7321, scheme II * |
The Journal of Organic Chemistry, vol. 54, no. 10, 12 May 1989 (US), Y. Le Merrer et al.: "Total synthesis of leukotriene B4[(+)-LTB4] and homo-LTB4 from D-mannitol", pages 2409 - 2416 * |
The Journal of Organic Chemistry, vol. 54, no. 10, 12 May 1989 (US), Y. Le Merrer et al.: "Total synthesis of leukotriene B4[(+)-LTB4] and homo-LTB4 from D-mannitol", pages 2409-2416, see page 2411, scheme IV * |
The Journal of Organic Chemistry, vol. 54, no. 22, 27 October 1989, American Chemical Soc. (US), A. Dureault et al.: ""Nucleophilic opening of chiral bis-(aziridines): a route to enantiomerically pure alpha-amino aldehydes or acids and polysubstituted piperidines", pages 5324 - 5330 * |
The Journal of Organic Chemistry, vol. 54, no. 22, 27 October 1989, American Chemical Soc. (US), A. Dureault et al.: ""Nucleophilic opening of chiral bis-(aziridines): a route to enantiomerically pure alpha-amino aldehydes or acids and polysubstituted piperidines", pages 5324-5330, see page 5324, column 1, line 1 - column 2, line 43, table 1, entries 7 and 8; page 5328, column 2, lines 19-43; scheme II * |
Also Published As
Publication number | Publication date |
---|---|
JPH07502970A (ja) | 1995-03-30 |
WO1991018866A2 (fr) | 1991-12-12 |
HU9203505D0 (en) | 1993-01-28 |
TW204336B (fr) | 1993-04-21 |
CA2084087A1 (fr) | 1991-12-02 |
BR9106540A (pt) | 1993-05-25 |
HUT64738A (en) | 1994-02-28 |
ZA914194B (en) | 1993-02-24 |
US5294720A (en) | 1994-03-15 |
EP0532693A1 (fr) | 1993-03-24 |
EP0665215A1 (fr) | 1995-08-02 |
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