Synthesis and NMR Analysis of 1,4‐Disubstituted 1,2,3‐Triazoles Tethered to Pyridine, Pyrimidine, and Pyrazine Rings

Abstract

AbstractA combinatorial modular approach based on the “click” copper(I)‐catalysed azide–alkyne cycloaddition reaction was used to prepare a library of selected 1,4‐disubstituted 1,2,3‐triazoles differently functionalized with heteroaryl groups including pyridine, pyrimidine, and pyrazine. Three different copper(I) sources, i.e., CuSO4/sodium ascorbate, CuBr(PPh3)3, and (CuOTf)2·C6H6 were used to promote the coupling reactions of a range of aryl, heteroaryl, and heteroarylmethyl azides with alkyne “click” partners. As the target heteroaryl triazoles were designed to serve as advanced ligands or ligand precursors for metal coordination, they were fully characterized by 1H, 13C, and 15N NMR spectroscopy. The resonances were assigned on the basis of 1D and 2D NMR experiments. 1H–15N gs‐HMBC was used as a practical tool to determine 15N NMR chemical shifts at the natural abundance level of the 15N isotope.