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Characteristics of the halogenation of 2-substituted 6-benzhydryl-4(3H)-pyrimidinones

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The halogenation of 2-substituted 6-benzhydryl-4(3H)-pyrimidinones has been investigated. Bromination with Py·Br2 and iodination with I2 solution in alkali occurs exclusively at the CH hydrogen of the benzhydryl group.

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Authors and Affiliations

  1. Volgograd State Technical University, Volgograd, 400131, Russia

    I. A. Novakov, B. S. Orlinson & M. B. Nawrozkij

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  1. I. A. Novakov
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  2. B. S. Orlinson
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  3. M. B. Nawrozkij
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, 1418–1420, September, 2006.

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Novakov, I.A., Orlinson, B.S. & Nawrozkij, M.B. Characteristics of the halogenation of 2-substituted 6-benzhydryl-4(3H)-pyrimidinones. Chem Heterocycl Compd 42, 1233–1235 (2006). https://doi.org/10.1007/s10593-006-0231-y

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  • DOI: https://doi.org/10.1007/s10593-006-0231-y

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