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盐酸氯卡色林消旋体的合成工艺改进
引用本文:王昊苏,朱亦龙,吴 飞,王德才. 盐酸氯卡色林消旋体的合成工艺改进[J]. 药学与临床研究, 2014, 22(3): 237-238
作者姓名:王昊苏  朱亦龙  吴 飞  王德才
作者单位:南京工业大学药学院,南京210009
摘    要:改进盐酸氯卡色林消旋体的合成工艺,以对氯苯乙腈为起始原料,经还原得到中间体对氯苯乙胺,与2-氯丙酰氯反应,再经傅克烷基化反应成环,然后使用硼氢化钠、三氯化铝还原体系还原酰胺,最后成盐,得到目标产物,总收率达25.0%。

关 键 词:盐酸氯卡色林消旋体  合成  减肥药
收稿时间:2014-01-16
修稿时间:2014-03-06

Improvement the Synthesis Process of Lorcaserin Hydrochloride Racemate
WANG Hao-su,ZHU Yi-long,WU Fei and WANG De-cai. Improvement the Synthesis Process of Lorcaserin Hydrochloride Racemate[J]. Pharmacertical and Clinical Research, 2014, 22(3): 237-238
Authors:WANG Hao-su  ZHU Yi-long  WU Fei  WANG De-cai
Affiliation:( School of Pharmaceutical Sciences, Nanjing University of Technology, Nanjing 210009, China)
Abstract:This study is to synthesize lorcaserin hydrochloride racemate and improve the process. The 4-chlorophenethylamine was synthesized from 4-chlorobenzyl cyanide by reduction, and then it was reacted with 2-chloropropionyl chloride, through cyclization, reduction by sodium borohydride and aluminum chloride,finally through salt formation, to form lorcaserin hydrochloride racemate, with an overall yield of 25.0%.
Keywords:Lorcaserin hydrochloride racemate  Synthesis  Antiobesity agent
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