Synthesis of Biologically Active Indenoisoquinoline Derivatives via a One-Pot Copper(II)-Catalyzed Tandem Reaction

J Org Chem. 2017 Feb 17;82(4):1961-1968. doi: 10.1021/acs.joc.6b02814. Epub 2017 Feb 8.

Abstract

A concise route for the synthesis of indenoisoquinoline derivatives from 2-iodobenzamide and 1,3-indanedione derivatives in the presence of copper(II) chloride and cesium carbonate in acetonitrile solvent is reported. A wide variety of 2-iodobenzamide derivatives and indandiones could be used to synthesize indenoisoquinoline derivatives and other fused indenoisoquinoline in moderate to good yields. This methodology was adapted for the one-step synthesis of a series of clinically active topoisomerase I inhibitors such as NSC 314622, LMP-400, LMP-776.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Copper / chemistry*
  • Crystallography, X-Ray
  • Indenes / chemical synthesis*
  • Indenes / chemistry
  • Isoquinolines / chemical synthesis*
  • Isoquinolines / chemistry
  • Models, Molecular
  • Molecular Structure

Substances

  • Indenes
  • Isoquinolines
  • indene
  • Copper
  • isoquinoline