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Synthesis of 5-substituted cyanofurans and their reaction with hydrazine

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Based on the Schmidt reaction, a new method has been developed for the preparation of nitriles in furan series from the corresponding furfural derivatives. Depending on conditions, the reaction of 5-substituted cyanofurans with hydrazine leads to amidrazones, N-aminotriazoles, or 1,2,4,5-dihydrotetrazines.

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Authors and Affiliations

  1. Krasnodar Polytechnical Institute, 350700, Krasnodar

    P. A. Pavlov & V. G. Kul'nevich

Authors
  1. P. A. Pavlov
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  2. V. G. Kul'nevich
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 181–186, February, 1986.

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Pavlov, P.A., Kul'nevich, V.G. Synthesis of 5-substituted cyanofurans and their reaction with hydrazine. Chem Heterocycl Compd 22, 140–145 (1986). https://doi.org/10.1007/BF00519931

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  • DOI: https://doi.org/10.1007/BF00519931

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