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公开(公告)号:US20140057836A1
公开(公告)日:2014-02-27
申请号:US13960343
申请日:2013-08-06
申请人: Thomas BARA , Sathesh Bhat , Dipshika Biswas , Linda Brockunier , Duane Burnette , Samuel Chackalamannil , Mariappan Vasu Cheliah , Austin Chen , Martin Clasby , Vince J. Colandrea , Zhuyan Guo , Yongxin Han , Charles Jayne , Hubert Josien , Karen Marcantonio , Shouwu Miao , Santhosh Neelamkavil , Patrick Pinto , Murali Rajogopalan , Unmesh Shah , Francisco Velazquez , Srikanth Venkatraman , Yan Xia
发明人: Thomas BARA , Sathesh Bhat , Dipshika Biswas , Linda Brockunier , Duane Burnette , Samuel Chackalamannil , Mariappan Vasu Cheliah , Austin Chen , Martin Clasby , Vince J. Colandrea , Zhuyan Guo , Yongxin Han , Charles Jayne , Hubert Josien , Karen Marcantonio , Shouwu Miao , Santhosh Neelamkavil , Patrick Pinto , Murali Rajogopalan , Unmesh Shah , Francisco Velazquez , Srikanth Venkatraman , Yan Xia
CPC分类号: C07K5/08 , A61K38/06 , A61K45/06 , C07D419/00 , C07D491/22
摘要: The present invention relates to hepatitis C virus (HCV) NS3 protease inhibitors containing a spirocyclic moeity, uses of such compounds, and synthesis of such compounds.
摘要翻译: 本发明涉及含有螺环状的丙型肝炎病毒(HCV)NS3蛋白酶抑制剂,这些化合物的用途,以及这些化合物的合成。
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2.Process for the Preparation of Pyridine Heterocycle Cgrp Antagonist Intermediate 审中-公开
标题翻译: 制备吡啶杂环Cgrp拮抗剂中间体的方法公开(公告)号:US20090176986A1
公开(公告)日:2009-07-09
申请号:US12226126
申请日:2007-04-06
IPC分类号: C07D471/04
CPC分类号: C07D471/04
摘要: An efficient syntheses for the preparation of the intermediate 2-oxo-1-(4-piperidinyl)-2,3-dihydro-1H-imidazo[4,5-b]pyridine dihydrochloride, and other salt forms of 2-oxo-1-(4-piperidinyl)-2,3-dihydro-1H-imidazo[4,5-b]pyridine.
摘要翻译: 制备中间体2-氧代-1-(4-哌啶基)-2,3-二氢-1H-咪唑并[4,5-b]吡啶二盐酸盐和其它盐形式的2-氧代-1 - (4-哌啶基)-2,3-二氢-1H-咪唑并[4,5-b]吡啶。
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