名称:
Synthesis of sterically hindered 3,5,5-trimethyl 2,6-dioxo tetrahydro pyrimidine as HCV protease inhibitors
摘要:
An efficient route for the synthesis of sterically hindered substituted and unsubstituted 2,6-dioxo tetra-hydropyrimidines from amine 1 is described. These analogs are active against HCV NS3 serine protease. The biological data for some of the representative examples are also reported. (C) 2009 Elsevier Ltd All rights reserved.
DOI:
10.1016/j.tetlet.2009.12.129