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1.发明授权Method for making intermediates useful in the synthesis of retroviral protease inhibitors 失效制备可用于合成逆转录病毒蛋白酶抑制剂的中间体的方法
公开(公告)号：US5648511A
公开(公告)日：1997-07-15
申请号：US452187
申请日：1995-05-25
申请人： John S. Ng , Claire A. Przybyla , Richard A. Mueller , Michael L. Vazquez , Daniel P. Getman , John J. Freskos , Gary A. DeCrescenzo , Deborah E. Bertenshaw , Robert M. Heintz , Suhong Zhang , Chin Liu , Scott A. Laneman
发明人： John S. Ng , Claire A. Przybyla , Richard A. Mueller , Michael L. Vazquez , Daniel P. Getman , John J. Freskos , Gary A. DeCrescenzo , Deborah E. Bertenshaw , Robert M. Heintz , Suhong Zhang , Chin Liu , Scott A. Laneman
IPC分类号： A61K31/17 , A61K31/195 , A61K31/197 , A61K31/27 , A61K31/47 , A61K31/4709 , A61K31/496 , A61K31/5377 , A61K38/00 , C07C213/00 , C07C213/02 , C07C213/08 , C07C215/28 , C07C269/04 , C07C269/06 , C07C271/16 , C07F7/18 , C07K5/078 , C07D253/00
CPC分类号： C07C269/06 , A61K31/17 , A61K31/195 , A61K31/197 , A61K31/27 , A61K31/47 , A61K31/4709 , A61K31/496 , A61K31/5377 , C07C213/00 , C07C213/02 , C07C213/08 , C07C269/04 , C07F7/188 , C07K5/06139 , A61K38/00 , C07B2200/07
摘要： A synthesis is described for intermediates which are readily amenable to the large scale preparation of hydroxyethylurea-based chiral HIV protease inhibitors. The method includes forming a diastereoselective epoxide or cyanohydrin from a chiral alpha amino aldehyde.
摘要翻译： 对于易于大规模制备基于羟基脲的手性HIV蛋白酶抑制剂的中间体描述了合成。 该方法包括由手性α氨基醛形成非对映选择性环氧化物或羟腈。
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公开(公告)号：US5872298A
公开(公告)日：1999-02-16
申请号：US833737
申请日：1997-04-09
申请人： John S Ng , Claire A Przybyla , Richard A Mueller , Michael L Vazquez , Daniel P Getman , John J Freskos , Gary A DeCrescenzo , Deborah E Bertenshaw , Robert M Heintz , Suhong Zhang , Chin Liu , Scott A Laneman
发明人： John S Ng , Claire A Przybyla , Richard A Mueller , Michael L Vazquez , Daniel P Getman , John J Freskos , Gary A DeCrescenzo , Deborah E Bertenshaw , Robert M Heintz , Suhong Zhang , Chin Liu , Scott A Laneman
IPC分类号： A61K31/17 , A61K31/195 , A61K31/197 , A61K31/27 , A61K31/47 , A61K31/4709 , A61K31/496 , A61K31/5377 , A61K38/00 , C07C213/00 , C07C213/02 , C07C213/08 , C07C215/28 , C07C269/04 , C07C269/06 , C07C271/16 , C07F7/18 , C07K5/078 , C07C311/27
CPC分类号： C07C269/06 , A61K31/17 , A61K31/195 , A61K31/197 , A61K31/27 , A61K31/47 , A61K31/4709 , A61K31/496 , A61K31/5377 , C07C213/00 , C07C213/02 , C07C213/08 , C07C269/04 , C07F7/188 , C07K5/06139 , A61K38/00 , C07B2200/07
摘要： A synthesis is described for intermediates which are readily amenable to the large scale preparation of hydroxyethylurea-based chiral HIV protease inhibitors. The method includes forming a diastereoselective epoxide or cyanohydrin from a chiral alpha amino aldehyde.
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公开(公告)号：US5872299A
公开(公告)日：1999-02-16
申请号：US854133
申请日：1997-05-08
申请人： John S Ng , Claire A Przybyla , Richard A Mueller , Michael L Vazquez , Daniel P Getman , John J Freskos , Gary A DeCrescenzo , Deborah E Bertenshaw , Robert M Heintz , Suhong Zhang , Chin Liu , Scott A Laneman
发明人： John S Ng , Claire A Przybyla , Richard A Mueller , Michael L Vazquez , Daniel P Getman , John J Freskos , Gary A DeCrescenzo , Deborah E Bertenshaw , Robert M Heintz , Suhong Zhang , Chin Liu , Scott A Laneman
IPC分类号： A61K31/17 , A61K31/195 , A61K31/197 , A61K31/27 , A61K31/47 , A61K31/4709 , A61K31/496 , A61K31/5377 , A61K38/00 , C07C213/00 , C07C213/02 , C07C213/08 , C07C215/28 , C07C269/04 , C07C269/06 , C07C271/16 , C07F7/18 , C07K5/078 , C07C211/27
CPC分类号： C07C269/06 , A61K31/17 , A61K31/195 , A61K31/197 , A61K31/27 , A61K31/47 , A61K31/4709 , A61K31/496 , A61K31/5377 , C07C213/00 , C07C213/02 , C07C213/08 , C07C269/04 , C07F7/188 , C07K5/06139 , A61K38/00 , C07B2200/07
摘要： A synthesis is described for intermediates which are readily amenable to the large scale preparation of hydroxyethylurea-based chiral HIV protease inhibitors. The method includes forming a diastereoselective epoxide or cyanohydrin from a chiral alpha amino aldehyde.
摘要翻译： 对于易于大规模制备基于羟基脲的手性HIV蛋白酶抑制剂的中间体描述了合成。 该方法包括由手性α氨基醛形成非对映选择性环氧化物或羟腈。
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