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1.Preparation of quinoline-substituted carbonate and carbamate derivatives 有权
Title translation: chinolinsubstituiertem碳酸酯和氨基甲酸酯衍生物的生产公开(公告)号:EP2261212A3
公开(公告)日:2014-12-31
申请号:EP10181265.9
申请日:2000-06-15
Applicant: ABBOTT LABORATORIES
Inventor: Allen, Michael S. , Premchandran, Ramiya H. , Chang, Sou-Jen , Condon, Stephen , Demattei, John J. , King, Steven A. , Kolaczkowski, Lawrence , Manna, Sukumar , Nichols, Paul J. , Patel, Hemant H. , Patel, Subhash R. , Plata, Daniel J. , Stoner, Eric J. , Tien, Jien-Heh J. , Wittenberger, Steven J.
IPC: C07D215/14 , C07C68/06 , C07C69/96 , C07C33/03
CPC classification number: C07D215/14 , C07C68/06 , C07C69/96
Abstract: The invention relates to a process for preparing quinoline-substituted carbonate and carbamate compounds, which are important intermediates in the synthesis of 6-O-suhstituted macrolide antibiotics. The process employs metal-catalyzed coupling reactions to provide a carbonate or carbamate of formula (I) or (II) or a substrate that can be reduced to obtain the same.
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公开(公告)号:EP0486948B1
公开(公告)日:2000-10-04
申请号:EP91119464.5
申请日:1991-11-04
Applicant: ABBOTT LABORATORIES
Inventor: Kempf, Dale J. , Codacovi, Lynn M. , Norbeck, Daniel W. , Plattner, Jacob J. , Sham, Hing L. , Wittenberger, Steven J. , Zhao, Chen
IPC: C07D213/26 , C07D213/30 , C07D213/40 , C07K5/06 , A61K38/55 , C07D213/56 , C07D211/16 , C07D295/20 , C07D277/30 , C07D277/42 , C07D417/12 , C07D277/40 , C07D401/12 , C07D277/24 , C07D277/28 , C07D235/14 , C07D235/16
CPC classification number: C07D213/30 , A61K38/00 , C07C53/134 , C07C215/18 , C07C215/20 , C07C215/28 , C07C233/40 , C07C237/10 , C07C237/22 , C07C271/20 , C07C271/22 , C07C271/34 , C07C275/24 , C07D213/26 , C07D213/34 , C07D213/40 , C07D213/54 , C07D213/56 , C07D213/61 , C07D213/75 , C07D231/12 , C07D233/56 , C07D233/64 , C07D233/84 , C07D235/14 , C07D235/16 , C07D239/26 , C07D241/12 , C07D249/08 , C07D261/08 , C07D263/32 , C07D277/24 , C07D277/28 , C07D277/30 , C07D277/36 , C07D277/40 , C07D277/42 , C07D277/56 , C07D295/13 , C07D295/205 , C07D295/215 , C07D303/36 , C07D307/42 , C07D333/16 , C07D401/12 , C07D413/10 , C07D417/12 , C07K5/06026 , C07K5/06078
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3.Preparation of quinoline-substituted carbonate and carbamate derivatives 有权
Title translation: on。。。。。。。。。。。。。公开(公告)号:EP2261212A2
公开(公告)日:2010-12-15
申请号:EP10181265.9
申请日:2000-06-15
Applicant: Abbott Laboratories
Inventor: Allen, Michael S. , Premchandran, Ramiya H. , Chang, Sou-Jen , Condon, Stephen , Demattei, John J. , King, Steven A. , Kolaczkowski, Lawrence , Manna, Sukumar , Nichols, Paul J. , Patel, Hemant H. , Patel, Subhash R. , Plata, Daniel J. , Stoner, Eric J. , Tien, Jien-Heh J. , Wittenberger, Steven J.
IPC: C07D215/14 , C07C68/06 , C07C69/96 , C07C33/03
CPC classification number: C07D215/14 , C07C68/06 , C07C69/96
Abstract: The invention relates to a process for preparing quinoline-substituted carbonate and carbamate compounds, which are important intermediates in the synthesis of 6-O-suhstituted macrolide antibiotics. The process employs metal-catalyzed coupling reactions to provide a carbonate or carbamate of formula (I) or (II) or a substrate that can be reduced to obtain the same.
Abstract translation: 本发明涉及一种制备喹啉取代的碳酸酯和氨基甲酸酯化合物的方法,其是合成6-O-取代的大环内酯类抗生素的重要中间体。 该方法使用金属催化的偶联反应来提供式(I)或(II)的碳酸酯或氨基甲酸酯或可以还原得到相同的底物。
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4.Benzo-1,3-dioxolyl- and benzofuranyl substituted pyrrolidine derivatives as endothelin antagonists 失效
Title translation: 苯并-1,3-二恶唑基 - 和苯并呋喃基取代的吡咯烷衍生物内皮素拮抗剂公开(公告)号:EP1609790A2
公开(公告)日:2005-12-28
申请号:EP05106190.1
申请日:1997-02-12
Applicant: ABBOTT LABORATORIES
Inventor: Winn, Martin , Henry, Kenneth J. Jr. , Liu, Gang , Wittenberger, Steven J. , King, Steven A. , Boyd, Steven A. , Hutchins, Charles W. , Jae, Hwan-Soo , Tasker, Andrew S. , Von Geldern, Thomas W. , Kester, Jeffrey A. , Sorensen, Bryan K. , Szczepankiewicz, Bruce G.
IPC: C07D405/04 , C07D405/12 , A61K31/40 , A61K31/41 , A61K31/435
CPC classification number: C07D401/04 , C07D207/16 , C07D405/04 , C07D405/12 , C07D405/14 , Y02P20/55
Abstract: A compound of formula (I), or a pharmaceutically acceptable salt thereof is disclosed, as well as processes for and intermediates in the preparation thereof, and a method of antagonizing endothelin.
Abstract translation: 公开了式(I)化合物或其药学上可接受的盐,以及其制备方法和中间体,以及拮抗内皮素的方法。
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公开(公告)号:EP0486948A3
公开(公告)日:1993-08-25
申请号:EP91119464.5
申请日:1991-11-04
Applicant: ABBOTT LABORATORIES
Inventor: Kempf, Dale J. , Codacovi, Lynn M. , Norbeck, Daniel W. , Plattner, Jacob J. , Sham, Hing L. , Wittenberger, Steven J. , Zhao, Chen
IPC: C07D213/26 , C07D213/30 , C07D213/40 , C07K5/06 , A61K37/64 , C07D213/56 , C07D211/16 , C07D295/20 , C07D277/30 , C07D277/42 , C07D417/12 , C07D277/40 , C07D401/12 , C07D277/24 , C07D277/28 , C07D235/14 , C07D235/16
CPC classification number: C07D213/30 , A61K38/00 , C07C53/134 , C07C215/18 , C07C215/20 , C07C215/28 , C07C233/40 , C07C237/10 , C07C237/22 , C07C271/20 , C07C271/22 , C07C271/34 , C07C275/24 , C07D213/26 , C07D213/34 , C07D213/40 , C07D213/54 , C07D213/56 , C07D213/61 , C07D213/75 , C07D231/12 , C07D233/56 , C07D233/64 , C07D233/84 , C07D235/14 , C07D235/16 , C07D239/26 , C07D241/12 , C07D249/08 , C07D261/08 , C07D263/32 , C07D277/24 , C07D277/28 , C07D277/30 , C07D277/36 , C07D277/40 , C07D277/42 , C07D277/56 , C07D295/13 , C07D295/205 , C07D295/215 , C07D303/36 , C07D307/42 , C07D333/16 , C07D401/12 , C07D413/10 , C07D417/12 , C07K5/06026 , C07K5/06078
Abstract: A retroviral protease inhibiting compound of the formula A -X- B is disclosed. Also disclosed are a composition and method for inhibiting a retroviral protease and for treating an HIV infection. Also disclosed are processes and intermediates useful for the preparation of the retroviral protease inhibitors.
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6.Intermediates for preparing retroviral protease inhibiting compounds 失效
Title translation: Zwischeprodukte用于逆转录病毒蛋白酶抑制剂的制备中公开(公告)号:EP0997459B1
公开(公告)日:2008-11-26
申请号:EP00101297.0
申请日:1991-11-04
Applicant: ABBOTT LABORATORIES
Inventor: Kempf, Dale J. , Codacovi, Lynn M. , Norbeck, Daniel W. , Plattner, Jacob J. , Sham, Hing L. , Wittenberger, Steven J. , Zhao, Chen
IPC: C07D277/24 , A61K31/425
CPC classification number: C07D213/30 , A61K38/00 , C07C53/134 , C07C215/18 , C07C215/20 , C07C215/28 , C07C233/40 , C07C237/10 , C07C237/22 , C07C271/20 , C07C271/22 , C07C271/34 , C07C275/24 , C07D213/26 , C07D213/34 , C07D213/40 , C07D213/54 , C07D213/56 , C07D213/61 , C07D213/75 , C07D231/12 , C07D233/56 , C07D233/64 , C07D233/84 , C07D235/14 , C07D235/16 , C07D239/26 , C07D241/12 , C07D249/08 , C07D261/08 , C07D263/32 , C07D277/24 , C07D277/28 , C07D277/30 , C07D277/36 , C07D277/40 , C07D277/42 , C07D277/56 , C07D295/13 , C07D295/205 , C07D295/215 , C07D303/36 , C07D307/42 , C07D333/16 , C07D401/12 , C07D413/10 , C07D417/12 , C07K5/06026 , C07K5/06078
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7.Benzo-1,3-dioxolyl- and benzofuranyl substituted pyrrolidine derivatives as endothelin antagonists 失效
Title translation: 苯并-1,3-二氧杂环戊烯和苯并呋喃基取代的吡咯烷衍生物作为内皮素拮抗剂公开(公告)号:EP1609790A3
公开(公告)日:2006-01-04
申请号:EP05106190.1
申请日:1997-02-12
Applicant: ABBOTT LABORATORIES
Inventor: Winn, Martin , Henry, Kenneth J. Jr. , Liu, Gang , Wittenberger, Steven J. , King, Steven A. , Boyd, Steven A. , Hutchins, Charles W. , Jae, Hwan-Soo , Tasker, Andrew S. , Von Geldern, Thomas W. , Kester, Jeffrey A. , Sorensen, Bryan K. , Szczepankiewicz, Bruce G.
IPC: C07D405/04 , C07D405/12 , A61K31/40 , A61K31/41 , A61K31/435
CPC classification number: C07D401/04 , C07D207/16 , C07D405/04 , C07D405/12 , C07D405/14 , Y02P20/55
Abstract: A compound of formula (I), or a pharmaceutically acceptable salt thereof is disclosed, as well as processes for and intermediates in the preparation thereof, and a method of antagonizing endothelin.
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8.Intermediates for preparing retroviral protease inhibiting compounds 失效
Title translation: Zwischeprodukte zur Herstellung von retroviralen Protease-Hemmern公开(公告)号:EP0997459A1
公开(公告)日:2000-05-03
申请号:EP00101297.0
申请日:1991-11-04
Applicant: Abbott Laboratories
Inventor: Kempf, Dale J. , Codacovi, Lynn M. , Norbeck, Daniel W. , Plattner, Jacob J. , Sham, Hing L. , Wittenberger, Steven J. , Zhao, Chen
IPC: C07D277/24 , A61K31/425
CPC classification number: C07D213/30 , A61K38/00 , C07C53/134 , C07C215/18 , C07C215/20 , C07C215/28 , C07C233/40 , C07C237/10 , C07C237/22 , C07C271/20 , C07C271/22 , C07C271/34 , C07C275/24 , C07D213/26 , C07D213/34 , C07D213/40 , C07D213/54 , C07D213/56 , C07D213/61 , C07D213/75 , C07D231/12 , C07D233/56 , C07D233/64 , C07D233/84 , C07D235/14 , C07D235/16 , C07D239/26 , C07D241/12 , C07D249/08 , C07D261/08 , C07D263/32 , C07D277/24 , C07D277/28 , C07D277/30 , C07D277/36 , C07D277/40 , C07D277/42 , C07D277/56 , C07D295/13 , C07D295/205 , C07D295/215 , C07D303/36 , C07D307/42 , C07D333/16 , C07D401/12 , C07D413/10 , C07D417/12 , C07K5/06026 , C07K5/06078
Abstract: An intermediate of the formula:
and
an intermediate of the formula:
or an acid addition salt thereof.Abstract translation: 下式的中间体:
和式:CHEM的中间体或其酸加成盐 -
公开(公告)号:EP0486948A2
公开(公告)日:1992-05-27
申请号:EP91119464.5
申请日:1991-11-04
Applicant: ABBOTT LABORATORIES
Inventor: Kempf, Dale J. , Codacovi, Lynn M. , Norbeck, Daniel W. , Plattner, Jacob J. , Sham, Hing L. , Wittenberger, Steven J. , Zhao, Chen
IPC: C07D213/26 , C07D213/30 , C07D213/40 , C07K5/06 , A61K37/64 , C07D213/56 , C07D211/16 , C07D295/20 , C07D277/30 , C07D277/42 , C07D417/12 , C07D277/40 , C07D401/12 , C07D277/24 , C07D277/28 , C07D235/14 , C07D235/16
CPC classification number: C07D213/30 , A61K38/00 , C07C53/134 , C07C215/18 , C07C215/20 , C07C215/28 , C07C233/40 , C07C237/10 , C07C237/22 , C07C271/20 , C07C271/22 , C07C271/34 , C07C275/24 , C07D213/26 , C07D213/34 , C07D213/40 , C07D213/54 , C07D213/56 , C07D213/61 , C07D213/75 , C07D231/12 , C07D233/56 , C07D233/64 , C07D233/84 , C07D235/14 , C07D235/16 , C07D239/26 , C07D241/12 , C07D249/08 , C07D261/08 , C07D263/32 , C07D277/24 , C07D277/28 , C07D277/30 , C07D277/36 , C07D277/40 , C07D277/42 , C07D277/56 , C07D295/13 , C07D295/205 , C07D295/215 , C07D303/36 , C07D307/42 , C07D333/16 , C07D401/12 , C07D413/10 , C07D417/12 , C07K5/06026 , C07K5/06078
Abstract: A retroviral protease inhibiting compound of the formula A -X- B is disclosed. Also disclosed are a composition and method for inhibiting a retroviral protease and for treating an HIV infection. Also disclosed are processes and intermediates useful for the preparation of the retroviral protease inhibitors.
Abstract translation: 公开了具有式A -X-B的逆转录病毒蛋白酶抑制化合物。 还公开了抑制逆转录病毒蛋白酶和治疗HIV感染的组合物和方法。 还公开了可用于制备逆转录病毒蛋白酶抑制剂的方法和中间体。
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