Synthesis of di/trifluoromethyl bis(1,2,4-triazoline)spiranes and 1,2,4-triazoles via 1,3-dipolar cycloaddition of nitrilimines and carbodiimides

Abstract

An efficient strategy for constructing di/trifluoromethyl bis(1,2,4-triazoline)spiranes and 1,2,4-triazoles via 1,3-dipolar cycloaddition reaction of nitrilimines and carbodiimides was developed. Various N-aryl di/trifluoromethyl acetohydrazonoyl bromides are well tolerated in the reaction, providing the target products in good regioselectivity and yields. This method features simple operation, high efficiency and mild reaction conditions for the rapid synthesis of complex fluoroalkylated nitrogen-rich spirocyclic compounds.

Graphical abstract: Synthesis of di/trifluoromethyl bis(1,2,4-triazoline)spiranes and 1,2,4-triazoles via 1,3-dipolar cycloaddition of nitrilimines and carbodiimides

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Article information

Article type
Paper
Submitted
12 Nov 2024
Accepted
31 Jan 2025
First published
05 Feb 2025

Org. Biomol. Chem., 2025, Advance Article

Synthesis of di/trifluoromethyl bis(1,2,4-triazoline)spiranes and 1,2,4-triazoles via 1,3-dipolar cycloaddition of nitrilimines and carbodiimides

Y. Zhou, X. Li, X. Liu, D. Huang, K. Wang, J. Wang and Y. Hu, Org. Biomol. Chem., 2025, Advance Article , DOI: 10.1039/D4OB01821D

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