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Synthesis of 3-S-hetaryl-substituted pyridin-2(1H)-ones and 5,6-dihydropyridin-2(1H)-ones*

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Chemistry of Heterocyclic Compounds Aims and scope

A method has been developed for the synthesis of 3-S-hetaryl-substituted pyridin-2(1H)-ones and 5,6-dihydropyridin-2(1H)-ones based on the base catalyzed cyclization of N-(3-oxoalkyl)- and N-(3-oxoalkenyl)amides which contain a divalent sulfur atom in an α-position to a carbamoyl group and bound to the heterocycle.

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Authors and Affiliations

  1. F. M. Dostoevsky Omsk State University, Omsk, 644077, Russia

    A. S. Fisyuk, Y. P. Bogza, N. V. Poendaev & D. S. Goncharov

Authors
  1. A. S. Fisyuk
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  2. Y. P. Bogza
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  3. N. V. Poendaev
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  4. D. S. Goncharov
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Correspondence to A. S. Fisyuk.

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* Dedicated to the memory of the prominent scientist and wise teacher, Reva S. Sagitullin.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 1044-1049, July, 2010.

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Fisyuk, A.S., Bogza, Y.P., Poendaev, N.V. et al. Synthesis of 3-S-hetaryl-substituted pyridin-2(1H)-ones and 5,6-dihydropyridin-2(1H)-ones*. Chem Heterocycl Comp 46, 844–849 (2010). https://doi.org/10.1007/s10593-010-0592-0

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  • DOI: https://doi.org/10.1007/s10593-010-0592-0

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