Synthesis and tautomerism of 2-(3,5-diaryl-1H-pyrazol-4-yl)-1-methyl-1H-benzimidazoles

  • I. B. DzvinchukEmail author
  • M. O. Lozinskii

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.


aroylhydrazines benzimidazoles pyrazoles tautomerism 


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Copyright information

© Springer Science+Business Media, Inc. 2011

Authors and Affiliations

  1. 1.Institute of Organic ChemistryNational Academy of SciencesKievUkraine

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