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Addition of heterocyclic CH acids to the C=N bond of azomethines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The aminomethylation of oxindole, 1-phenyl-3-methyl-5-pyrazolone, and N-phenyl-rhodanine was studied. Derivatives of these CH acids were obtained as a result of aminomethylation. The addition products were subjected to acid and base hydrolysis; the corresponding arylidene derivatives are formed in the case of the products of aminomethylation of oxindole and 1-phenyl-3-methyl-5-pyrazolone, while thioglycolic acids are formed in the case of N-phenylrhodanine derivatives.

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Authors and Affiliations

  1. Donetsk State University, 340055, Donetsk

    N. I. Pavlenko, V. P. Marshtupa, N. A. Klyuev & B. P. Baskunov

Authors
  1. N. I. Pavlenko
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  2. V. P. Marshtupa
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  3. N. A. Klyuev
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  4. B. P. Baskunov
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1088–1093, August, 1981.

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Pavlenko, N.I., Marshtupa, V.P., Klyuev, N.A. et al. Addition of heterocyclic CH acids to the C=N bond of azomethines. Chem Heterocycl Compd 17, 808–812 (1981). https://doi.org/10.1007/BF00503664

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  • DOI: https://doi.org/10.1007/BF00503664

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