Issue 11, 2024

Efficient and metal-free synthesis of 2-aroyl 7-azaindoles via thermally induced denitrogenative intramolecular annulation of 1,2,3,4-tetrazolopyridines

Abstract

A facile and metal-free intramolecular denitrogenative annulation strategy for the preparation of novel 2-aroyl 7-azaindoles has been developed from 3-(tetrazolo[1,5-a]pyridin-8-yl)prop-2-en-1-one in the presence of the deep eutectic solvent Dowtherm A. The valuable features of the protocol include a short reaction time, absence of any metal catalyst, utilization of a eutectic solvent, easy product isolation, and very good yields of novel 2-aroyl 7-azaindoles.

Graphical abstract: Efficient and metal-free synthesis of 2-aroyl 7-azaindoles via thermally induced denitrogenative intramolecular annulation of 1,2,3,4-tetrazolopyridines

Supplementary files

Article information

Article type
Communication
Submitted
15 Jan 2024
Accepted
20 Feb 2024
First published
27 Feb 2024

Org. Biomol. Chem., 2024,22, 2192-2196

Efficient and metal-free synthesis of 2-aroyl 7-azaindoles via thermally induced denitrogenative intramolecular annulation of 1,2,3,4-tetrazolopyridines

C. A. Chamakiya, S. R. Chothani, R. J. Joshi, J. Bhalodia, M. A. Ambasana, A. H. Bapodra and N. Kapuriya, Org. Biomol. Chem., 2024, 22, 2192 DOI: 10.1039/D4OB00078A

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