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Design and synthesis of bicyclic pyrimidinone-based HCV NS3 protease inhibitors
Authors:Glunz Peter W  Douty Brent D  Decicco Carl P
Institution:Bristol-Myers Squibb Pharmaceutical Research Institute, PO Box 5400, Princeton, NJ 08543-5400, USA. peter.glunz@bms.com
Abstract:A series of bicyclic pyrimidinone-based HCV NS3 protease inhibitors was synthesized via selective C8 position functionalization. Substituted phenylamides and phenylureas were preferred in the S2 binding pocket.
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