首页 | 本学科首页   官方微博 | 高级检索  
     

(S)-1-(2-氯乙酰基)吡咯烷-2-甲腈的合成与表征
引用本文:王延安,马玉卓. (S)-1-(2-氯乙酰基)吡咯烷-2-甲腈的合成与表征[J]. 精细化工中间体, 2010, 40(1): 27-30
作者姓名:王延安  马玉卓
作者单位:广东药学院,药科学院,广东,广州,510006
摘    要:探讨了合成(S)-1-(2-氯乙酰基)吡咯烷-2-甲腈的新工艺路线,即以L-脯氨酸为原料,经N-氯乙酰化、羧基氨基化和酰胺脱水反应合成目标化合物。目标化合物及各中间体的结构采用1HNMR和MS进行了确定。此外,详细研究了反应条件的影响,得到了优化的反应条件。目标产物的总收率可达42.3%。该合成路线具有原料便宜易得、操作简单、条件温和等优点,具有很好的市场应用前景。

关 键 词:合成  L-脯氨酸  (S)-1-(2-氯乙酰基)吡咯烷-2-甲腈  二肽基肽酶Ⅳ

Synthesis and Characterization of (S)-1-(2-Chloroacetyl) pyrrolidine- 2-carbonitrile
WANG Yon-an,MA Yu-zhuo. Synthesis and Characterization of (S)-1-(2-Chloroacetyl) pyrrolidine- 2-carbonitrile[J]. Fine Chemical Intermediates, 2010, 40(1): 27-30
Authors:WANG Yon-an  MA Yu-zhuo
Affiliation:(College of Pharmacy, Guangdong Pharmaceutical University, Guangzhou 510006, China)
Abstract:(S)- 1- (2-Chloroacetyl) pyrrolidine-2-carbonitrile was synthesized from L-proline via the processes ot N-chloroacetion, cabboxyl amination and earboxamide dehydration. The structures of the intermediates and the target compound were confirmed by 1H NMR and MS. Effect of the process conditions on reaction was investigated and the optimum parameters were obtained. The target compound was achieved in an oveval yield of 42.3%. The synthetic route has advantage of lower cost, simple operation and mild reaction condition.
Keywords:synthesis  L-proline  (S)- 1- (2-chloroacetyl) pyrrolidine-2-earbonitrile  DPP-Ⅳ
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号