Paper
Tandem Michael addition/imino-nitrile cyclization synthesis of 2-amino-6-(1-aryl-5-methyl-1H-1,2,3-triazol-4yl)-4-phenylpyridine-3-carbonitrile
Published Mar 1, 2010 · Heng-Shan Dong, Huicheng Wang, Zhong‐Lian Gao
Journal of Heterocyclic Chemistry
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Abstract
Several 2–amino-6-(1-aryl-5-methyl-1H-1,2,3-triazol-4-yl)-4-phenylpyridine-3-carbonitrile have been synthesized by Tandem Michael addition/imino-nitrile cyclization and the structures of these compounds were established by MS, IR, CHN, and 1H NMR spectral data. The crystal structure of 2-amino-6-[1-(4-methoxyphenyl)-5-methyl-1H-1,2,3-triazol-4-yl]-4-phenylpyridine-3-carbonitrile was established by X-ray diffraction. J. Heterocyclic Chem., (2010).
Tandem Michael addition/imino-nitrile cyclization effectively synthesizes 2-amino-6-(1-aryl-5-methyl-1H-1,2,3-triazol-4yl)-4-phenylpyridine-3-carbonitrile, with structures established by MS, IR,
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