Synthesis of benzo[f]isoindole-4,9-diones

J Org Chem. 2008 Oct 3;73(19):7555-9. doi: 10.1021/jo801056e. Epub 2008 Sep 6.

Abstract

A synthesis of benzo[f]isoindole-4,9-diones 1 is presented starting from the reaction of 2,3-bis(bromomethyl)-1,4-dimethoxynaphthalene 15 with primary amines affording 2,3-bis(aminomethyl)-1,4-dimethoxynaphthalenes 14, which could be converted by CAN-mediated oxidation in one step to benzo[f]isoindole-4,9-diones 1. An alternative synthesis of benzo[f]isoindole-4,9-diones 1 starts from 2,3-bis(bromomethyl)-1,4-naphthoquinone 9 via 2,3-dihydrobenzo[f]isoindoles 10 which spontaneously oxidize.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Products / chemistry
  • Isoindoles / chemical synthesis*
  • Naphthalenes / chemistry
  • Oxidation-Reduction
  • Quinones / chemistry

Substances

  • Biological Products
  • Isoindoles
  • Naphthalenes
  • Quinones