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Research on imidazo[1,2-a]benzimidazole derivatives

19. Action of excess nitrous acid on 9-methyl-2-phenylimidazo[1,2-a]benzimidazole

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The action of excess nitrous acid on 9-methyl-2-phenylimidazo[1,2-a]benzimidazole results in opening of the outer imidazole ring and the formation of unstable 1-methyl-2-nitrosimino-3-oximinophenacylbenzimidazoline. The products of cleavage of this compound in alkali, acid, and alcohol solutions were studied.

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Authors and Affiliations

  1. Scientific-Research Institute of Physical and Organic Chemistry, Rostov State University, 344006, Rostov-on-Don

    V. A. Anisimova & A. M. Simonov

Authors
  1. V. A. Anisimova
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  2. A. M. Simonov
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Additional information

See [1] for Communication 18.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 68–70, January, 1980.

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Anisimova, V.A., Simonov, A.M. Research on imidazo[1,2-a]benzimidazole derivatives. Chem Heterocycl Compd 16, 57–59 (1980). https://doi.org/10.1007/BF00475393

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  • DOI: https://doi.org/10.1007/BF00475393

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