申请人:Hollingsworth I. Rawle
公开号:US20070265451A1
公开(公告)日:2007-11-15
A process for preparing N-(substituted)-C-(substituted methyl)-oxazolidinones, C-(substituted methyl)-oxazolidinones, and N-(substituted)-C-(substituted methyl)-oxazolidinones, preferably chiral, from optically active C-(protected oxymethyl)-oxazolidinones is described. The process can be used to produce combinatorial libraries of the above substituted oxazolidinones in a two or three step reaction comprising a plurality of reagents differing in numbers of carbons or particular substituted oxazolidinones. A number of substituted oxazolidinones produced using the above process have been discovered to have antimicrobial activity.
本文介绍了一种从光学活性的C-(保护的氧甲基)-噁唑烷酮制备N-(取代)-C-(取代甲基)-噁唑烷酮、C-(取代甲基)-噁唑烷酮和N-(取代)-C-(取代甲基)-噁唑烷酮的方法,其中优选手性化合物。该方法可用于在包含多种碳数或特定取代噁唑烷酮的多种试剂的两步或三步反应中产生上述取代噁唑烷酮的组合库。使用上述方法生产的许多取代噁唑烷酮已被发现具有抗微生物活性。