Issue 98, 2017

Imidazole synthesis by transition metal free, base-mediated deaminative coupling of benzylamines and nitriles

Abstract

A transition metal free, straightforward synthetic method for the preparation of substituted imidazoles is reported herein. Base promoted, deaminative coupling of benzylamines with nitriles results in the one-step synthesis of 2,4,5-trisubstituted imidazoles with liberation of ammonia. This protocol provides a practical strategy for the synthesis of valuable imidazole derivatives from readily available starting materials.

Graphical abstract: Imidazole synthesis by transition metal free, base-mediated deaminative coupling of benzylamines and nitriles

Supplementary files

Article information

Article type
Communication
Submitted
28 Oct 2017
Accepted
14 Nov 2017
First published
14 Nov 2017

Chem. Commun., 2017,53, 13133-13136

Imidazole synthesis by transition metal free, base-mediated deaminative coupling of benzylamines and nitriles

U. K. Das, L. J. W. Shimon and D. Milstein, Chem. Commun., 2017, 53, 13133 DOI: 10.1039/C7CC08322J

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