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免疫促进剂匹多莫德的合成改进
引用本文:李秀珍,王赟,商志才,俞庆森.免疫促进剂匹多莫德的合成改进[J].化学世界,2005,46(9):555-557.
作者姓名:李秀珍  王赟  商志才  俞庆森
作者单位:浙江大学化学系,浙江,杭州,310027
摘    要:以L-半胱氨酸、L-焦谷氨酸为起始原料,经三步合成了匹多莫德.在传统的合成方法基础上进行了一定的改进,即在第二步的酯化反应中采用了冰浴条件下向无水甲醇中滴加CH3COCl,得到甲醇的HCl溶液,在其未达到饱和状态时仍取得了比较好的酯化结果,提高了产率,适合工业化.

关 键 词:免疫促进剂  匹多莫德  L-半胱氨酸  L-焦谷氨酸
文章编号:0367-6358(2005)09-555-03
收稿时间:2004-07-26
修稿时间:2004-07-262004-08-25

An Improvement on the Synthesis of Pidotimod
LI Xiu-zhen,WANG Yun,SHANG Zhi-cai,YU Qing-sen.An Improvement on the Synthesis of Pidotimod[J].Chemical World,2005,46(9):555-557.
Authors:LI Xiu-zhen  WANG Yun  SHANG Zhi-cai  YU Qing-sen
Abstract:Pidotimod, ara immunomodulator was synthesized in a three-step process with L-cysteine and L-pyroglutamic acid as starting materials. In this method, acetyl chloride was added to absolute methanol drop wise at the ice-bath temperature and an unsaturated solution of hydrogen chloride in methanol was obtained in the second step. This method gives good yield and is well adapted to industrialization
Keywords:immunomodulator  pidotimod  L-cysteine  L-pyroglutamic acid
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