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Research in the chemistry of heterocyclic quinoneimines. 3. Oxidative cyclization of 2,5-diarylamino-substituted 1,4-benzoquinone-4-phenylimines — Simple method for the preparation of 2-arylamino-5-aryl-3-phenazinones

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

2,5-Diarylamino-1,4-benzoquinone-4-phenylimines, which are formed in the reaction of 1,4-benzoquinone-4-phenylimine with aromatic amines, are converted under oxidative conditions to products of intramolecular oxidative cyclization, viz., 2-arylamino-5-aryl-3-phenazinones.

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Authors and Affiliations

  1. S. M. Kirov Ural Polytechnic Institute, 620002, Sverdlovsk

    E. V. Tsoi, G. B. Afanas'eva & O. N. Chupakhin

Authors
  1. E. V. Tsoi
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  2. G. B. Afanas'eva
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  3. O. N. Chupakhin
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Additional information

See [4] for Communication 2.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 330–333, March, 1984.

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Tsoi, E.V., Afanas'eva, G.B. & Chupakhin, O.N. Research in the chemistry of heterocyclic quinoneimines. 3. Oxidative cyclization of 2,5-diarylamino-substituted 1,4-benzoquinone-4-phenylimines — Simple method for the preparation of 2-arylamino-5-aryl-3-phenazinones. Chem Heterocycl Compd 20, 263–267 (1984). https://doi.org/10.1007/BF00515634

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  • DOI: https://doi.org/10.1007/BF00515634

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