Issue 35, 2023

Synthesis of fused 3-trifluoromethyl-1,2,4-triazoles via base-promoted [3 + 2] cycloaddition of nitrile imines and 1H-benzo[d]imidazole-2-thiols

Abstract

Here we report a strategy for the facile assembly of fused 3-trifluoromethyl-1,2,4-triazoles, which are difficult to synthesize using traditional strategies, in 50–96% yields through a triethylamine-promoted intermolecular [3 + 2] cycloaddition pathway. This protocol features high efficiency, good functional group tolerance, mild conditions, and easy operation. Furthermore, a gram-scale reaction and product derivatizations were carried out smoothly to illustrate the practicability of this method.

Graphical abstract: Synthesis of fused 3-trifluoromethyl-1,2,4-triazoles via base-promoted [3 + 2] cycloaddition of nitrile imines and 1H-benzo[d]imidazole-2-thiols

Supplementary files

Article information

Article type
Communication
Submitted
17 Jul 2023
Accepted
18 Aug 2023
First published
18 Aug 2023

Org. Biomol. Chem., 2023,21, 7095-7099

Synthesis of fused 3-trifluoromethyl-1,2,4-triazoles via base-promoted [3 + 2] cycloaddition of nitrile imines and 1H-benzo[d]imidazole-2-thiols

K. Cen, J. Wei, Y. Feng, Y. Liu, X. Wang, Y. Liu, Y. Yin, J. Yu, D. Wang and J. Cai, Org. Biomol. Chem., 2023, 21, 7095 DOI: 10.1039/D3OB01133J

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