Thiazole formation through a modified Gewald reaction.

Journal: Beilstein Journal Of Organic Chemistry
Published:
Abstract

The synthesis of thiazoles and thiophenes starting from nitriles, via a modified Gewald reaction has been studied for a number of different substrates. 1,4-Dithiane-2,5-diol was used as the aldehyde precursor to give either 2-substituted thiazoles or 2-substituted aminothiophenes depending on the substitution of the α-carbon to the cyano group.

Authors
Carl Mallia, Lukas Englert, Gary Walter, Ian Baxendale