Itoh Takahiro, Mase Toshiaki
Process Research, PreClinical Development, Banyu Pharmaceutical Co., Ltd., 3 Okubo, Tsukuba, Ibaraki, 300-2611, Japan.
Org Lett. 2007 Aug 30;9(18):3687-9. doi: 10.1021/ol7015737. Epub 2007 Aug 9.
A convenient synthesis of substituted benzothiazoles from 2-bromoanilides has been accomplished. The various 2-bromoanilides were reacted with an alkyl thiolate in high yields using a palladium catalyst. The resulting sulfides were easily converted to the corresponding benzothiazoles via the simultaneous generation of thiols and condensation under basic or acidic conditions.
已实现了从2-溴代苯胺合成取代苯并噻唑的简便方法。使用钯催化剂,各种2-溴代苯胺与硫醇盐以高收率反应。通过在碱性或酸性条件下同时生成硫醇并缩合,所得硫化物可轻松转化为相应的苯并噻唑。