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Quinone Imines with a Fused Azine Ring: III. Synthesis and Reactivity of 8-p-Tolylsulfonylimino-5,8-dihydroquinolin-5-one Derivatives

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Abstract

Unstable 8-p-tolylsulfonylimino-5,8-dihydroquinolin-5-one was generated by oxidation of the corresponding reduced form in acetic acid; it reacted in situ with hydrogen chloride and sodium p-toluenesulfinate to give the corresponding 6-substituted 5-hydroxy-8-aminoquinolines.

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Authors and Affiliations

  1. Ukrainian State University of Chemical Technology, pr. Gagarina 8, Dnepropetrovsk, 49005, Ukraine

    A. V. Belov & V. M. Nichvoloda

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  1. A. V. Belov
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  2. V. M. Nichvoloda
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Translated from Zhurnal Organicheskoi Khimii, Vol. 41, No. 1, 2005, pp. 124–127.

Original Russian Text Copyright © 2005 by Belov, Nichvoloda.

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Belov, A.V., Nichvoloda, V.M. Quinone Imines with a Fused Azine Ring: III. Synthesis and Reactivity of 8-p-Tolylsulfonylimino-5,8-dihydroquinolin-5-one Derivatives. Russ J Org Chem 41, 124–127 (2005). https://doi.org/10.1007/s11178-005-0133-y

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  • DOI: https://doi.org/10.1007/s11178-005-0133-y

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