ARTICLE

Copper-Catalyzed Synthesis of Benzofuropyrimidoisoindole Derivatives

  • Heng He ,
  • Lanlan Lü ,
  • Jianquan Liu ,
  • Xiangshan Wang
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  • School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou, Jiangsu 221116
*Corresponding authors. E-mail:;

Received date: 2024-04-05

  Revised date: 2024-05-14

  Online published: 2024-06-13

Supported by

Outstanding Youth Fund of Jiangsu Province(BK20211607); Priority Academic Program Development of Jiangsu Higher Education Institutions.

Abstract

A copper-catalyzed Sonogashira coupling reaction and 5-exo-dig aminocyclization between 2-(2-bromophenyl)- benzofuro[3,2-d]pyrimidin-4(3H)-ones and terminal alkynes were disclosed. The protocol allowed access to a series of 8-benzylidene benzofuro[3',2':4,5]pyrimido[2,1-a]isoindol-6(8H)-one derivatives with high efficiency, broad substrate scope, and excellent functional group compatibility, which were shown to be of a single (E)-configuration by X-ray diffraction analysis.

Cite this article

Heng He , Lanlan Lü , Jianquan Liu , Xiangshan Wang . Copper-Catalyzed Synthesis of Benzofuropyrimidoisoindole Derivatives[J]. Chinese Journal of Organic Chemistry, 2024 , 44(11) : 3427 -3436 . DOI: 10.6023/cjoc202404005

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