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公开(公告)号:WO0020441A3
公开(公告)日:2000-11-23
申请号:PCT/US9922844
申请日:1999-10-01
Applicant: ABBOTT LAB
Inventor: WANG WEI-BO , LI QUN , HASVOLD LISA A , CHEN HUI-JU , LI LEPING , LARTEY PAUL A , CLAIBORNE AKIYO , STEINER BETH A , BENNANI YOUSSEF , DICKMAN DANIEL , DING HONG
IPC: C07C67/343 , C07D295/155 , C07K7/56 , A61K38/12 , A61P33/08
CPC classification number: C07D295/155 , C07C67/343 , C07K7/56 , C07C69/94
Abstract: The invention relates to a novel cyclic hexapeptide having antifungal and antipneumocystic activity as well as pharmaceutical compositions comprising, methods of treating using, and a process for preparing the claimed compounds.
Abstract translation: 本发明涉及具有抗真菌和抗肺囊虫活性的新型环状六肽以及药物组合物,其包含使用方法和制备所要求保护的化合物的方法。
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公开(公告)号:WO0181316A3
公开(公告)日:2002-05-23
申请号:PCT/US0113678
申请日:2001-04-25
Applicant: ABBOTT LAB
Inventor: WANG WEI-BO , CURTIN MICHAEL L , FAKHOURY STEPHEN A , GWALTNEY STEPHEN L II , HASVOLD LISA A , HUTCHINS CHARLES W , LI QUI , LIN NAN-HORNG , JENNINGS NELSON LISSA TAKA , O'CONNOR STEPHEN J , SHAM HING L , SULLIVAN GERALD M , WANG GARY T , WANG XILU
IPC: C07D233/22 , A61K31/381 , A61K31/415 , A61K31/4164 , A61K31/4178 , A61K31/4245 , A61K31/426 , A61K31/4406 , A61K31/4412 , A61K31/443 , A61K31/4436 , A61K31/4439 , A61K31/444 , A61K31/454 , A61K31/4545 , A61K31/4709 , A61K31/496 , A61P17/06 , A61P27/02 , A61P27/06 , A61P29/00 , A61P35/00 , A61P35/02 , A61P37/06 , A61P43/00 , C07D213/30 , C07D213/36 , C07D213/38 , C07D213/40 , C07D213/42 , C07D213/57 , C07D213/61 , C07D213/64 , C07D213/80 , C07D213/82 , C07D213/84 , C07D213/85 , C07D231/12 , C07D233/26 , C07D233/54 , C07D249/04 , C07D249/08 , C07D277/20 , C07D277/24 , C07D277/28 , C07D277/30 , C07D333/16 , C07D333/24 , C07D401/06 , C07D401/10 , C07D401/12 , C07D401/14 , C07D405/10 , C07D405/12 , C07D409/10 , C07D413/10 , C07D413/12 , C07D417/06 , C07D417/10 , C07D417/12 , A61K31/33 , C07D213/74 , C07D409/12
CPC classification number: C07D213/30 , C07D213/36 , C07D231/12 , C07D233/64 , C07D249/04 , C07D249/08 , C07D277/24 , C07D277/28 , C07D277/30 , C07D333/16 , C07D333/24 , C07D401/06 , C07D401/10 , C07D401/12 , C07D401/14 , C07D409/10 , C07D413/12 , C07D417/06
Abstract: Compounds of formula (I) or pharmaceutically acceptable salts thereof, inhibit farnesyltransferase. Methods for making the compounds, pharmaceutical compositions containing the compounds, and methods of treatment using the compounds are disclosed.
Abstract translation: 式(I)化合物或其药学上可接受的盐抑制法呢基转移酶。 公开了制备该化合物的方法,含该化合物的药物组合物和使用该化合物的治疗方法。
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公开(公告)号:ES2168740T3
公开(公告)日:2002-06-16
申请号:ES98904979
申请日:1998-02-06
Applicant: ABBOTT LAB
Inventor: WANG WEI-BO , KERDESKY FRANCIS A J , HSIAO CHI-NUNG W , LI QUN , CHU DANIEL T
IPC: C07D455/02
Abstract: A process for the preparation of a compound having the formula: wherein R1, R2, R3, R4, and R5 are defined, from an enamine by chain expansion and ring closure followed by additional derivatization, treatment with a 3-alkoxyl-acryloyl compound, another ring closure, and converting a hydroxyl group to a leaving group.
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公开(公告)号:CZ288199A3
公开(公告)日:1999-11-17
申请号:CZ288199
申请日:1998-02-06
Applicant: ABBOTT LAB
Inventor: WANG WEI-BO , KERDESKY FRANCIS A J , HSAIO CHI-NUNG W , LI QUN , CHU DANIEL T
IPC: C07D455/02
Abstract: A process for the preparation of a compound having the formula: wherein R1, R2, R3, R4, and R5 are defined, from an enamine by chain expansion and ring closure followed by additional derivatization, treatment with a 3-alkoxyl-acryloyl compound, another ring closure, and converting a hydroxyl group to a leaving group.
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公开(公告)号:TR9901956T2
公开(公告)日:1999-10-21
申请号:TR9901956
申请日:1998-02-06
Applicant: ABBOTT LAB
Inventor: WANG WEI-BO , KERDESKY FRANCIS A J , HSIAO CHI-NUNG W , LI QUN , CHU DANIEL T
IPC: C07D455/02
CPC classification number: C07D455/02
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公开(公告)号:ZA979728B
公开(公告)日:1998-05-22
申请号:ZA979728
申请日:1997-10-29
Applicant: ABBOTT LAB
Inventor: WANG WEI-BO , LI QUN , CHU DANIEL T , HASVOLD LISA ANNE
IPC: C07D207/14 , C07D455/02 , C07D471/04 , C07D
Abstract: A process for the preparation of chiral 3-aminopyrrolidine and analogous bicyclic derivatives from dihydroxy olefins by treatment with titanium isopropoxide, an optically active tartrate ester and tert-butyl hydroperoxide, followed by subsequent alkylation of the intermediate with an alkyl or alkenyl magnesium halide, then pyrrolidine ring formation by condensation with an arylmethylamine, subsequent chiral replacement of a ring hydroxyl group with an amino group with further protection thereof, optional additional substitution closing of the second ring, and hydrogenolysis to remove a ring-nitrogen protecting group.
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公开(公告)号:CZ290252B6
公开(公告)日:2002-06-12
申请号:CZ288199
申请日:1998-02-06
Applicant: ABBOTT LAB
Inventor: WANG WEI-BO , KERDESKY FRANCIS A J , HSIAO CHI-NUNG W , LI QUN , CHU DANIEL T
IPC: C07D455/02
Abstract: In the present invention there is disclosed a process for preparing carboxylic acid of the general formula II, in which the substituents Re1 through Re5 have specific meaning, by reacting enamine with acid chloride and further by reacting the resulting intermediate with malonamic acid ester in the presence of a base. Subsequently the obtained compound is protected on the hydroxy position by treatment thereof for example with methyl chloride. The resulting compound then reacts with an alkali metal base and subsequently with 3-alkoxyacryloyl compound and the formed intermediates is reacted with a catalytic amount of acid in order to close a ring and finally the resulting acid is reacted with a halogenating agent.
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公开(公告)号:CA2407093A1
公开(公告)日:2001-11-01
申请号:CA2407093
申请日:2001-04-25
Applicant: ABBOTT LAB
Inventor: GWALTNEY STEPHEN L II , SULLIVAN GERALD M , WANG GARY T , FAKHOURY STEPHEN A , HUTCHINS CHARLES W , LI QUN , SHAM HING L , HASVOLD LISA A , WANG XILU , LIN NAN-HORNG , CURTIN MICHAEL L , WANG WEI-BO , O'CONNOR STEPHEN J , JENNINGS NELSON LISSA TAKA
IPC: C07D233/22 , A61K31/381 , A61K31/415 , A61K31/4164 , A61K31/4178 , A61K31/4245 , A61K31/426 , A61K31/4406 , A61K31/4412 , A61K31/443 , A61K31/4436 , A61K31/4439 , A61K31/444 , A61K31/454 , A61K31/4545 , A61K31/4709 , A61K31/496 , A61P17/06 , A61P27/02 , A61P27/06 , A61P29/00 , A61P35/00 , A61P35/02 , A61P37/06 , A61P43/00 , C07D213/30 , C07D213/36 , C07D213/38 , C07D213/40 , C07D213/42 , C07D213/57 , C07D213/61 , C07D213/64 , C07D213/80 , C07D213/82 , C07D213/84 , C07D213/85 , C07D231/12 , C07D233/26 , C07D233/54 , C07D249/04 , C07D249/08 , C07D277/20 , C07D277/24 , C07D277/28 , C07D277/30 , C07D333/16 , C07D333/24 , C07D401/06 , C07D401/10 , C07D401/12 , C07D401/14 , C07D405/10 , C07D405/12 , C07D409/10 , C07D413/10 , C07D413/12 , C07D417/06 , C07D417/10 , C07D417/12 , A61K31/33 , C07D213/74 , C07D409/12
Abstract: Compounds of formula (I) or pharmaceutically acceptable salts thereof, inhib it farnesyltransferase. Methods for making the compounds, pharmaceutical compositions containing the compounds, and methods of treatment using the compounds are disclosed.
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公开(公告)号:TR199901956T2
公开(公告)日:1999-10-21
申请号:TR9901956
申请日:1998-02-06
Applicant: ABBOTT LAB
Inventor: WANG WEI-BO , KERDESKY FRANCIS A J , HSIAO CHI-NUNG W , LI QUN , CHU DANIEL T
IPC: C07D455/02
Abstract: A process for the preparation of a compound having the formula: wherein R1, R2, R3, R4, and R5 are defined, from an enamine by chain expansion and ring closure followed by additional derivatization, treatment with a 3-alkoxyl-acryloyl compound, another ring closure, and converting a hydroxyl group to a leaving group.
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公开(公告)号:ZA9709728B
公开(公告)日:1998-05-22
申请号:ZA9709728
申请日:1997-10-29
Applicant: ABBOTT LAB
Inventor: WANG WEI-BO , LI QUN , CHU DANIEL T , HASVOLD LISA ANNE
IPC: C07D207/14 , C07D455/02 , C07D471/04 , C07D
CPC classification number: C07D207/14 , C07D455/02 , C07D471/04 , Y02P20/55
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