Issue 25, 2017

Visible-light-mediated C3-azolylation of imidazo[1,2-a]pyridines with 2-bromoazoles

Abstract

The C3-azolylation of imidazo[1,2-a]pyridines was developed via a visible light-mediated reaction of imidazopyridines with 2-bromoazoles catalyzed by Ir(ppy)2(dtbbpy)PF6 under mild conditions. For the imidazo[1,2-a]pyridines with various substituents on benzene or the pyridine ring and a variety of azoles, the reaction proceeded smoothly to give 3-(azol-2-yl)imidazo[1,2-a]pyridines in moderate to good yields.

Graphical abstract: Visible-light-mediated C3-azolylation of imidazo[1,2-a]pyridines with 2-bromoazoles

Supplementary files

Article information

Article type
Paper
Submitted
09 Apr 2017
Accepted
06 Jun 2017
First published
07 Jun 2017

Org. Biomol. Chem., 2017,15, 5318-5324

Visible-light-mediated C3-azolylation of imidazo[1,2-a]pyridines with 2-bromoazoles

Q. Chang, Z. Wu, L. Yu, P. Liu and P. Sun, Org. Biomol. Chem., 2017, 15, 5318 DOI: 10.1039/C7OB00883J

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