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Modification of biologically active amides and amines with fluorine-containing heterocycles 7. Fluorine-containing heterocyclic derivatives of the acetazolamide

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Abstract

An approach is proposed to modification of a medical product acetazolamide (N-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)acetamide) by interaction of 2-(5-acetylamino-1,3,4-thiadiazole-2-yl)sulfonyl imine methyl trifluoropyruvate, which is in-situ generated from acetazolamide, with 1,3-binucleophiles: 6-aminouracils, 6-aminothiouracils, and N-substituted ureas, to yield heterocyclic compounds with the CF3 substituent in the nitrogen-containing mono- or bicycle.

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Authors and Affiliations

  1. Institute of Physiologically Active Substances, Russian Academy of Sciences, 1 Severnyi proezd, 142432, Chernogolovka, Moscow Region, Russian Federation

    V. B. Sokolov & A. Yu. Aksinenko

Authors
  1. V. B. Sokolov
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  2. A. Yu. Aksinenko
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Correspondence to V. B. Sokolov.

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Report 6 see lit.

Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2108–2111, November, 2012.

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Sokolov, V.B., Aksinenko, A.Y. Modification of biologically active amides and amines with fluorine-containing heterocycles 7. Fluorine-containing heterocyclic derivatives of the acetazolamide. Russ Chem Bull 61, 2124–2128 (2012). https://doi.org/10.1007/s11172-012-0297-x

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  • DOI: https://doi.org/10.1007/s11172-012-0297-x

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