In this study, we report an efficient and straightforward protocol for the synthesis of 1,2,3-trisubstituted triazoles catalyzed by an N-heterocyclic carbene (NHC)–Copper(I) complex. While numerous methods exist for constructing the triazole core, our approach uniquely combines operational simplicity with high regioselectivity and excellent catalytic efficiency. The desired triazole derivatives were obtained in consistently high yields ranging from 85% to 94%, demonstrating the robustness, reproducibility, and practical utility of the method.

NHCs have emerged as highly versatile ligands and organocatalysts, owing to their strong σ-donating ability, tunable steric profiles, and remarkable stability under a wide range of reaction conditions. In the context of copper-catalyzed azide–alkyne cycloaddition (CuAAC) reactions, NHC–Cu(I) complexes have shown superior catalytic performance by enhancing reaction rates, minimizing side reactions, and enabling mild, scalable reaction conditions. This catalytic system effectively facilitates the selective synthesis of 1,2,3-trisubstituted triazoles with a broad substrate scope and operational ease.

This work highlights the synthetic value of NHC–Cu(I) catalysis for the efficient construction of trisubstituted triazole frameworks, which serve as important scaffolds in medicinal chemistry, chemical biology, and materials science. The developed method provides a sustainable, user-friendly, and highly selective route for accessing these heterocycles, underscoring its potential for broad application in the synthesis of complex molecules and functional materials.