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Quinoxaline-benzimidazole rearrangements in the reactions of 3-alkanoylquinoxalin-2-ones with 1,2-phenylenediamines

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Abstract

The interaction of 3-alkanoylquinoxalin-2-ones with 1,2-phenylenediamines in boiling acetic acid led to the contraction of the pyrazine ring as the result of a quinoxaline-benzimidiazole rearrangement with the formation of 2-benzimidazolyl-substituted quinoxalines.

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Correspondence to V. A. Mamedov.

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, 1539–1547, October, 2007.

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Kalinin, A.A., Isaikina, O.G. & Mamedov, V.A. Quinoxaline-benzimidazole rearrangements in the reactions of 3-alkanoylquinoxalin-2-ones with 1,2-phenylenediamines. Chem Heterocycl Comp 43, 1307–1314 (2007). https://doi.org/10.1007/s10593-007-0198-3

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  • DOI: https://doi.org/10.1007/s10593-007-0198-3

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