Direct C–H amidation of 1,3-azoles: light-mediated, photosensitiser-free vs. thermal

Abstract

We have developed one thermal and one light-mediated method for direct Minisci-type C–H amidation of 1,3-azoles, which are applicable to thiazoles, benzothiazoles, benzimidazoles, and for the first time, imidazoles. The new visible light-mediated approach can be rendered photosensitiser/photocatalyst-free and likely proceeds via an electron donor–acceptor (EDA) complex, the first direct Minisci-type amidation to do so.

Graphical abstract: Direct C–H amidation of 1,3-azoles: light-mediated, photosensitiser-free vs. thermal

Supplementary files

Article information

Article type
Communication
Submitted
05 יונ 2024
Accepted
13 אוג 2024
First published
19 אוג 2024
This article is Open Access
Creative Commons BY license

Chem. Commun., 2024, Advance Article

Direct C–H amidation of 1,3-azoles: light-mediated, photosensitiser-free vs. thermal

D. T. Mooney, H. McKee, T. S. Batch, S. Drane, P. R. Moore and A. Lee, Chem. Commun., 2024, Advance Article , DOI: 10.1039/D4CC02742F

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