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Condensation of 1-acylpyrazolines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Under the influence of phosphorus oxychloride, 1-acylpyrazolines condense to give 3-pyrazolinylpyrazoles; cleavage of the pyrazoline molecule occurs at the C3-N2 bond.

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Literature cited

  1. A. N. Kost, G. A. Golubeva, L. A. Sviridova, I. I. Grandberg, and N. B. Chernysheva, Dokl. Akad. Nauk SSSR, 179, 337 (1968).

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  2. N. S. Kozlov and V. D. Pak, Zh. Obshch. Khim., 32, 3386 (1962).

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Authors and Affiliations

  1. M. V. Lomonosov Moscow State University, USSR

    A. N. Kost, G. A. Golubeva, L. A. Sviridova & S. B. Goncharenko

Authors
  1. A. N. Kost
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  2. G. A. Golubeva
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  3. L. A. Sviridova
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  4. S. B. Goncharenko
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1268–1270, September, 1974.

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Kost, A.N., Golubeva, G.A., Sviridova, L.A. et al. Condensation of 1-acylpyrazolines. Chem Heterocycl Compd 10, 1102–1104 (1974). https://doi.org/10.1007/BF00472135

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  • DOI: https://doi.org/10.1007/BF00472135

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