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New synthesis of 3,5-diaryl-1,2,4-oxadiazoles containing a sulfonyl chloride or sulfonamide group

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Abstract

A procedure has been developed for the indirect introduction of sulfonyl chloride and sulfonamide groups into 3,5-diaryl-1,2,4-oxadiazoles via acylation of N′-hydroxybenzimidamide with aromatic and heterocyclic sulfocarboxylic acid dichlorides. The acylation selectively involves the carbonyl chloride group, regardless of the dichloride structure.

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Authors and Affiliations

  1. Yaroslavl State Technical University, Moskovskii pr. 88, Yaroslavl, 150999, Russia

    P. A. Agat’ev, R. M. Shlenev, A. V. Tarasov & A. S. Danilova

Authors
  1. P. A. Agat’ev
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  2. R. M. Shlenev
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  3. A. V. Tarasov
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  4. A. S. Danilova
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Corresponding author

Correspondence to P. A. Agat’ev.

Additional information

Original Russian Text © P.A. Agat’ev, R.M. Shlenev, A.V. Tarasov, A.S. Danilova, 2015, published in Zhurnal Organicheskoi Khimii, 2015, Vol. 51, No. 7, pp. 1006–1009.

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Agat’ev, P.A., Shlenev, R.M., Tarasov, A.V. et al. New synthesis of 3,5-diaryl-1,2,4-oxadiazoles containing a sulfonyl chloride or sulfonamide group. Russ J Org Chem 51, 988–991 (2015). https://doi.org/10.1134/S1070428015070167

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  • DOI: https://doi.org/10.1134/S1070428015070167

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