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Synthesis and Structure of Quaternary Salts Derived from 2-Anilino- and 2-Benzylamino-5,6-dihydro-4H-1,3-thiazine

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Abstract

Substituted phenacyl bromides react with 2-anilino-5,6-dihydro-4H-1,3-thiazine at the exocyclic nitrogen atom and with 2-benzylamino-5,6-dihydro-4H-1,3-thiazine at the nitrogen atom in the ring. The structure of the reaction intermediates was elucidated, and their cyclization into 1-benzyl-2-aryl-6,7-dihydro-5H-imidazo[2,1-b][1,3]thiazinium bromides was performed.

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Authors and Affiliations

  1. Shevchenko Pedagogical University, Chernigov, Ukraine

    A. M. Demchenko, S. I. Bova, V. A. Chumakov, A. N. Krasovskii, E. B. Rusanov, A. N. Chernega & M. O. Lozinskii

  2. Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kiev, Ukraine

    A. M. Demchenko, S. I. Bova, V. A. Chumakov, A. N. Krasovskii, E. B. Rusanov, A. N. Chernega & M. O. Lozinskii

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  1. A. M. Demchenko
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  2. S. I. Bova
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  3. V. A. Chumakov
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  4. A. N. Krasovskii
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  5. E. B. Rusanov
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  6. A. N. Chernega
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  7. M. O. Lozinskii
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Demchenko, A.M., Bova, S.I., Chumakov, V.A. et al. Synthesis and Structure of Quaternary Salts Derived from 2-Anilino- and 2-Benzylamino-5,6-dihydro-4H-1,3-thiazine. Russian Journal of General Chemistry 71, 1759–1763 (2001). https://doi.org/10.1023/A:1013998526065

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  • DOI: https://doi.org/10.1023/A:1013998526065

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