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Alkylation of 2-(hydroxyimino)-5H-[1,3]thiazolo[3,2-a]-pyrimidin-3(2H)-ones

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Abstract

Alkylation products were obtained from ethyl 2-(hydroxyimino)-7-methyl-3-oxo-5-aryl-2,3- dihydro-5H-[1,3]thiazolo[3,2-a]pyrimidin-6-carboxylates at the treatment with alkyl halides, dimethyl sulfate, and diazomethane. Diazomethane alkylated the initial substrate at the oxygen atom of the carbonyl group of the thiazolidine fragment, the other reagents, at the oxygen atom of the hydroxyimino group.

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Authors and Affiliations

  1. Samara State Technical University, Molodogvardeiskaya ul. 244, Samara, 443100, Russia

    E. A. Lashmanova, V. S. Larina & A. K. Shiryaev

Authors
  1. E. A. Lashmanova
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  2. V. S. Larina
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  3. A. K. Shiryaev
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Correspondence to E. A. Lashmanova.

Additional information

Original Russian Text © E.A. Lashmanova, V.S. Larina, A.K. Shiryaev, 2017, published in Zhurnal Organicheskoi Khimii, 2017, Vol. 53, No. 8, pp. 1233–1236.

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Lashmanova, E.A., Larina, V.S. & Shiryaev, A.K. Alkylation of 2-(hydroxyimino)-5H-[1,3]thiazolo[3,2-a]-pyrimidin-3(2H)-ones. Russ J Org Chem 53, 1249–1252 (2017). https://doi.org/10.1134/S1070428017080152

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  • DOI: https://doi.org/10.1134/S1070428017080152

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