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Uncommon reaction of 2-bromomethyl-1,3-thiaselenole with pyridine and its derivatives

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Abstract

Regioselective reaction of 2-bromomethyl-1,3-thiaselenole with pyridine and its derivatives is followed by rearrangement with ring expansion and the formation of a bond between a nitrogen atom and a carbon in the position 2. A set of derivatives of 2,3-dihydro-1,4-thiaselenine was obtained, substituted in the position 2 by a pyridinium residue functionalized by pharmacophoric groups.

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Authors and Affiliations

  1. Favorskii Irkutsk Institute of Chemistry, Siberian Branch, Russian Academy of Sciences, ul. Favorskogo 1, Irkutsk, 664033, Russia

    S. V. Amosova, M. V. Penzik, Yu. I. Rykunova, V. A. Potapov & A. I. Albanov

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  1. S. V. Amosova
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  2. M. V. Penzik
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  3. Yu. I. Rykunova
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  4. V. A. Potapov
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  5. A. I. Albanov
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Corresponding author

Correspondence to S. V. Amosova.

Additional information

Original Russian Text © S.V. Amosova, M.V. Penzik, Yu.I. Rykunova, V.A Potapov, A.I. Albanov, 2017, published in Zhurnal Organicheskoi Khimii, 2017, Vol. 53, No. 11, pp. 1655–1658.

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Amosova, S.V., Penzik, M.V., Rykunova, Y.I. et al. Uncommon reaction of 2-bromomethyl-1,3-thiaselenole with pyridine and its derivatives. Russ J Org Chem 53, 1691–1695 (2017). https://doi.org/10.1134/S1070428017110148

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  • DOI: https://doi.org/10.1134/S1070428017110148

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