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Reaction of 3,4-diiodo-2,5-dimethyl-1H-pyrrole with thioamides

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Abstract

3,4-Diiodo-2,5-dimethyl-1H-pyrrole reacted with thioacetamide in polar solvents or under solvent-free conditions to give 2,4,6-trimethyl-5H-pyrrolo[3,4-d][1,3]thiazole. The major product in the reaction of the title compound with thiobenzamide was 3,5-diphenyl-1,2,4-thiadiazole.

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Authors and Affiliations

  1. Lomonosov Moscow State University of Fine Chemical Technologies, pr. Vernadskogo 86, Moscow, 119571, Russia

    O. V. Kharitonova, T. A. Solomentseva, I. S. Golubtsov & A. F. Mironov

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  1. O. V. Kharitonova
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  2. T. A. Solomentseva
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  3. I. S. Golubtsov
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  4. A. F. Mironov
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Correspondence to O. V. Kharitonova.

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Original Russian Text © O.V. Kharitonova, T.A. Solomentseva, I.S. Golubtsov, A.F. Mironov, 2014, published in Zhurnal Organicheskoi Khimii, 2014, Vol. 50, No. 1, pp. 52–54.

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Kharitonova, O.V., Solomentseva, T.A., Golubtsov, I.S. et al. Reaction of 3,4-diiodo-2,5-dimethyl-1H-pyrrole with thioamides. Russ J Org Chem 50, 45–47 (2014). https://doi.org/10.1134/S1070428014010084

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  • DOI: https://doi.org/10.1134/S1070428014010084

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