Issue 10, 2016

Isonitrile alkylations: a rapid route to imidazo[1,5-a]pyridines

Abstract

Metalated arylmethylisonitriles readily add to 2-chloropyridines to afford imidazo[1,5-a]pyridines. Analogous additions to imidoyl chlorides and a chloroquinoline provide imidazoles and an imidazo[1,5-a]quinolone which, like imidazo[1,5-a]pyridines, are valuable heterocycles for pharmaceutical synthesis.

Graphical abstract: Isonitrile alkylations: a rapid route to imidazo[1,5-a]pyridines

Supplementary files

Article information

Article type
Communication
Submitted
20 Oct 2015
Accepted
17 Dec 2015
First published
22 Dec 2015

Chem. Commun., 2016,52, 2111-2113

Author version available

Isonitrile alkylations: a rapid route to imidazo[1,5-a]pyridines

Y. Li, A. Chao and F. F. Fleming, Chem. Commun., 2016, 52, 2111 DOI: 10.1039/C5CC08724D

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