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Reaction of substituted 1-hydroxy-4-hydroxylaminoimidazolidin-2-one with aryl isocyanates

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Various variants of reactions involving the carbamoylation of 1-hydroxy-3-(3′-chlorophenyl)-5,5-dimethyl-4-hydroxylaminoimidazolidin-2-one, which has three nucleophilic centers, viz., the N- and O-hydroxylamino groups and the O-hydroxyurea fragment of the molecule, were studied. Depending on the reaction conditions, mono-, and di-, and tricarbamoyl derivatives of substituted 4-hydroxyl-aminoimidazolidin-2-one were synthesized.

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Literature cited

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Authors and Affiliations

  1. All-Union Scientific-Research Institute of Chemical Agents for the Protection of Plants, 109088, Moscow

    S. P. Épshtein, A. F. Rukasov, V. P. Tashchi, P. M. Bashtrykov & Yu. G. Putsykin

Authors
  1. S. P. Épshtein
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  2. A. F. Rukasov
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  3. V. P. Tashchi
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  4. P. M. Bashtrykov
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  5. Yu. G. Putsykin
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1115–1119, August, 1983.

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Épshtein, S.P., Rukasov, A.F., Tashchi, V.P. et al. Reaction of substituted 1-hydroxy-4-hydroxylaminoimidazolidin-2-one with aryl isocyanates. Chem Heterocycl Compd 19, 897–900 (1983). https://doi.org/10.1007/BF00516460

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  • DOI: https://doi.org/10.1007/BF00516460

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