Issue 13, 2021

Synthesis of 5-trifluoromethyl-1,2,3-triazoles via base-mediated cascade annulation of diazo compounds with trifluoroacetimidoyl chlorides

Abstract

A metal-, azide- and CF3-reagent free approach for the synthesis of 5-trifluoromethyl-1,2,3-triazoles via base-mediated cascade annulation of diazo compounds with trifluoroacetimidoyl chlorides has been developed. Notable advantages of the reaction include readily available reagents, mild reaction conditions, a broad substrate scope, high efficiency, and promising synthetic utility. The protocol could be scaled up to the gram scale and be applied to construct the key skeleton of the analogue of LCRF-0004.

Graphical abstract: Synthesis of 5-trifluoromethyl-1,2,3-triazoles via base-mediated cascade annulation of diazo compounds with trifluoroacetimidoyl chlorides

Supplementary files

Article information

Article type
Research Article
Submitted
20 Mar 2021
Accepted
29 Apr 2021
First published
30 Apr 2021

Org. Chem. Front., 2021,8, 3440-3445

Synthesis of 5-trifluoromethyl-1,2,3-triazoles via base-mediated cascade annulation of diazo compounds with trifluoroacetimidoyl chlorides

H. Yang, T. Xu, S. Lu, Z. Chen and X. Wu, Org. Chem. Front., 2021, 8, 3440 DOI: 10.1039/D1QO00445J

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