Synthesis and tautomerism of 2-(3,5-diaryl-1H-pyrazol-4-yl)-1-methyl-1H-benzimidazoles |
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Authors: | I. B. Dzvinchuk M. O. Lozinskii |
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Affiliation: | (1) Institute of Organic Chemistry, National Academy of Sciences, Kiev, 02094, Ukraine |
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Abstract: | The cyclocondensation of 1-methyl-2-phenacyl-1H-benzimidazole with aroylhydrazines yields 2-(3,5-diaryl-1H-pyrazol-4-yl)-1-methyl-1H-benzimidazoles. The 1H NMR spectra indicate that these products display tautomerism. The more stable tautomers have structures containing electron-donor aryl substituents at C-5 and electron-withdrawing aryl substituents at C-3 of the pyrazole ring. |
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