应用化学 ›› 2011, Vol. 28 ›› Issue (03): 263-266.DOI: 10.3724/SP.J.1095.2011.00327

• 研究论文 • 上一篇    下一篇

2种吲哚衍生物的N-烷基化产物的制备

马文康,卢杏萍,黄雁*,罗健东*   

  1. (广州医学院基础学院 广州 510182)
  • 收稿日期:2010-06-07 修回日期:2010-07-22 出版日期:2011-03-10 发布日期:2011-03-10
  • 通讯作者: 黄雁,教授; Tel:020-81340209; Fax:020-81340163; E-mail:drhuangyan@163.com; 研究方向:细胞周期检验点废除剂的合成
  • 基金资助:
    广东省科技计划项目(2008B060600074)及广州市属高校科技计划项目(08A107)

N-Alkylations of Two Indole Derivatives

MA Wenkang, LU Xingping, HUANG Yan*, LUO Jiandong*   

  1. (Department of Foundation,Guangzhou Medical College,Guangzhou  510182)
  • Received:2010-06-07 Revised:2010-07-22 Published:2011-03-10 Online:2011-03-10

摘要:

吲哚-3-乙醛酸甲酯和3-吲哚乙腈在碱存在下,以烷基卤或硫酸烷基酯为亲电试剂进行N-烷基化反应,合成了6种新的N-烷基化吲哚化合物。 研究了吲哚化合物及烷基化试剂的结构、溶剂和碱对N-烷基化反应的影响。 具有强吸电子取代基的吲哚-3-乙醛酸甲酯使用弱碱Cs2CO3在室温就可顺利进行烷基化反应,产率达到93%;而具有较弱吸电子取代基的3-吲哚乙腈,需要使用强碱NaH才能进行烷基化反应。

关键词: 吲哚类化合物, N-烷基化, 合成

Abstract:

The N-alkylations of methyl 3-indoleglyoxylate and indole-3-acetonitrile were carried out using alkyl halides or sulfonates as electrophiles in the presence of bases and six new N-alkylation products of indole derivatives were prepared. The influences of the structures of indole derivatives and electrophiles, the solvents and bases on the alkylations have been studied. The N-alkylation of methyl 3-indoleglyoxylate with a strong electron-withdrawing group could be conducted using weak base Cs2CO3 in mild reaction condition and in 93% yields while a strong base such as NaH must be used when indole-3-acetonitrile with a weak electron-withdrawing group was used as reactant in the N-alkylation.

Key words: indole derivatives, N-alkylation, synthesis

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