微波辐射下5-取代-2-硫代海因衍生物的合成  

Synthesis of 5-Substituted-2-thiohydantoin Derivatives under Microwave Irradiation

作　　者：周佳栋[1] 曹飞[1] 武红丽[1] 韦萍[1] 

机构地区：[1]南京工业大学制药与生命科学学院,南京210009

出　　处：《有机化学》2008年第2期228-233,共6页Chinese Journal of Organic Chemistry

基　　金：国家重点基础研究发展计划(973计划)(No.2003CB7160004)资助项目

摘　　要：微波辐射下,由硫氰酸铵与α-氨基酸通过两步反应合成了11种5-取代-2-硫代海因衍生物,并用1HNMR,IR和元素分析确证了中间产物和终产物的结构.对比常规加热方法,微波辐射具有反应时间短(4min),每步反应产率高(85%～93%)的优点.同时对合成化合物2h的反应历程进行了讨论.Eleven 5-substituted-2-thiohydantoin derivatives were synthesized by a two-step reaction of ammonium thiocyanate with a-amino acids under microwave irradiation. The structures of intermediate products and final products were characterized by 1H NMR, IR spectra and elemental analysis. Compared with conventional heating method, microwave irradiation possessed such advantages as short reaction time （4 min）, high yield of each step （85%-93%）. In the meantime, the reaction course of synthesis of compound 2h was discussed.

关 键 词：5-取代-2-硫代海因 5-取代-1-乙酰基-2-硫代海因 硫氰酸铵 Α-氨基酸 微波辐射 

分 类 号：TQ463.2[化学工程—制药化工]