无配体条件下1,2,4-三唑的室温n -芳基化反应

Nikhil V. Suramwar, S. R. Thakare, N. T. Khaty
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引用次数: 3

摘要

在无配体条件下,利用优势面(111)纳米CuO作为催化剂,建立了一种简单有效的室温下1,2,4-三唑n -芳基化反应方法。该催化剂具有可回收性,多种底物均可在短时间内以高收率生成n -芳基化产物。这种催化剂的广泛范围使我们研究涉及活性较低的氮亲核试剂的转化,如咪唑和吡唑。我们很高兴地发现,各种唑衍生物与芳基碘化物有效地偶联,以优异的收率提供所需的n -芳基化产物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Room Temperature N-Arylation of 1,2,4-Triazoles under Ligand-Free Condition
A simple and efficient method for N-arylation of 1,2,4-triazole at room temperature was described by the use of predominant (111) facet CuO nanoparticles as a catalyst in ligand-free condition. The catalyst was recyclable, and a variety of substrates give N-arylation product in high yield with short period of reaction time. The wide scope of this catalyst led us to investigate transformations involving less-reactive nitrogen nucleophiles, such as imidazole and pyrazoles. We were pleased to find that various derivatives of azoles were effectively coupled with aryl iodide to afford the desired N-arylated product in excellent yield.
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