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Nitrile splitting in 2-amino-1-(arylmethyleneamino)-5-aryl-3,4-dicyanopyrroles

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Nitrile splitting of the N−N bond with formation of 2-amino-5-aryl-3,4-dicyanopyrroles and the corresponding benzonitrile occurs when 2-amino-5-aryl-1-(arylmethyleneamino)3,4-dicyanopyrroles are boiled in DMSO in the presence of alkali.

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References

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Authors
  1. A. N. Lyshchikov
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  2. Ya. S. Kayukov
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  3. O. V. Pul'kherovskaya
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  4. A. N. Vasil'ev
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  5. O. E. Nasakin
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Additional information

N. I. Ul'yanov Chuvash State University, Cheboksary 428015, Russia; e-mail:anatoly5@chuvs.ru. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1627–1629, December, 1999.

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Lyshchikov, A.N., Kayukov, Y.S., Pul'kherovskaya, O.V. et al. Nitrile splitting in 2-amino-1-(arylmethyleneamino)-5-aryl-3,4-dicyanopyrroles. Chem Heterocycl Compd 35, 1423–1425 (1999). https://doi.org/10.1007/BF02251815

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  • DOI: https://doi.org/10.1007/BF02251815

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