应用化学 ›› 2016, Vol. 33 ›› Issue (10): 1175-1181.DOI: 10.11944/j.issn.1000-0518.2016.10.160127

• 研究论文 • 上一篇    下一篇

铜催化苯甲酰胺有氧环化合成7-叔烷基异喹啉二酮

邓佑林,唐石(),李立洋,付美玲,王良能,陈蓝艳,周上睿   

  1. 吉首大学化学化工学院 湖南 吉首 416000
  • 收稿日期:2016-03-28 接受日期:2016-06-20 出版日期:2016-10-08 发布日期:2016-10-08
  • 通讯作者: 唐石
  • 基金资助:
    国家自然基金资助项目(21462017),吉首大学研究生科研创新项目资助(JGY201636),吉首大学科技处研究生科研项目(15JDY001),湖南省研究生培养创新基地(2014KFXM06)

Synthesis of 7-tert-Alkylated Isoquinolinedione via Copper-catalyzed Aerobic Cyclization of Benzamides

DENG Youlin,TANG Shi(),LI Liyang,FU Meiling,WANG Liangneng,CHEN Lanyan,ZHOU Shangrui   

  1. College of Chemistry and Chemical Engineering,Jishou University,Jishou,Hu'nan 416000,China
  • Received:2016-03-28 Accepted:2016-06-20 Published:2016-10-08 Online:2016-10-08
  • Contact: TANG Shi
  • Supported by:
    Supported by the National Natural Science Foundation of China(No.21462017), the Research Innovation Program for Graduates of Jishou University(No.JGY201636), the Research Program for Graduates of Science and Technology Department of Jishou University(No.15JDY001), the Hu'nan Innovation Base for the Graduate Student Training(No.2014KFXM06)

摘要:

发展了一种高效、简单的铜/空气催化体系催化的苯甲酰胺串联自由基环化合成7-叔烷基异喹啉二酮的反应。 在廉价CuI存在下,空气环境中,N-烷基-N-甲基丙烯酰基苯甲酰胺与AIBN发生串联自由基加成/环化/碳碳偶联反应,以52%~73%的产率合成了一系列的7-取代异喹啉二酮。 此研究为合成具有潜在药用价值的含氰取代异喹啉二酮提供了一条快速、简单、温和的构建途径。

关键词: 叔烷基异喹啉二酮, 苯甲酰胺, 有氧环化, 铜催化

Abstract:

A cheap and simple radical cyclization reaction of benzamides toward 7-tert-alkylated isoquinolinedione was developed. In the presence of cheap CuI and air, various N-alkyl-N-methacryloyl benzamides with azodiisobutyronitrile underwent cascade radical addition/cyclization/C-C coupling reactions, leading to a series of biologically active isoquinolinediones in the yields of 73% to 52%. This study provides a rapid, simple and mild entry to the synthesis of pharmaceutically interesting isoquinolindiones.

Key words: tert-alkylated isoquinolindione, benzamide, aerobic cyclization, copper catalysis