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4-Functionally-substituted 3-heterylpyrazoles: XVII. 3-Aryl-1-phenyl-4-pyrazolmethylsulfanyl(sulfinyl, sulfonyl)acetic acids

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Abstract

3-Aryl-1-phenyl-4-mercaptomethylpyrazoles reacted with monochloroacetic acid to give 3-aryl-1-phenyl-4-pyrazolylmethylsulfanylacetic acids whose oxidation with hydrogen peroxide in acetone or acetic acid solution led to 3-aryl-1-phenyl-4-pyrazolylmethylsulfinyl-and sulfonylacetic acids, respectively.

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Authors and Affiliations

  1. Bukovinskaya State Medical Academy, Chernovtsy, Ukraine

    M. K. Bratenko & V. A. Chornous

  2. Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kiev, 02094, Ukraine

    M. V. Vovk

Authors
  1. M. K. Bratenko
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  2. V. A. Chornous
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  3. M. V. Vovk
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Additional information

Original Russian Text © M.K. Bratenko, V.A. Chornous, M.V. Vovk, 2006, published in Zhurnal Organicheskoi Khimii, 2006, Vol. 42, No. 5. pp. 721–724.

For Communication XVI, see [1].

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Bratenko, M.K., Chornous, V.A. & Vovk, M.V. 4-Functionally-substituted 3-heterylpyrazoles: XVII. 3-Aryl-1-phenyl-4-pyrazolmethylsulfanyl(sulfinyl, sulfonyl)acetic acids. Russ J Org Chem 42, 703–706 (2006). https://doi.org/10.1134/S1070428006050101

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  • DOI: https://doi.org/10.1134/S1070428006050101

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