Transition metal-free synthesis of quinazolinones using dimethyl sulfoxide as a synthon

Org Biomol Chem. 2019 Sep 21;17(35):8067-8070. doi: 10.1039/c9ob01629e. Epub 2019 Aug 27.

Abstract

Biologically important quinazolinones have been synthesized from 2-aminobenzamides and DMSO. The key feature of the reaction is the utilization of DMSO as a methine source for intramolecular oxidative annulation. The CNS depressant drug methaqualone has also been synthesized by our methodology. The present method involves the synthesis of quinazolinones with a broad substrate scope and a good yield.

Publication types

  • Research Support, Non-U.S. Gov't