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4,5-Dihydroxyimidazolidin-2-ones in α-ureidoalkylation of N-carboxyalkyl-, N-hydroxyalkyl-, and N-aminoalkylureas 5. Synthesis of N-hydroxyalkyl-1,5-diphenylglycolurils

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Abstract

A systematic investigation of α-ureidoalkylation of N-hydroxyalkylureas with 4,5-dihydroxy-1,3-dimethyl-4,5-diphenylimidazolidin-2-one allowed the discovery of a synthetic route to earlier unknown N-hydroxyalkyl-1,5-diphenylglycolurils. The yields of these compounds decrease with lengthening and branching of the alkyl chain in the starting ureas.

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Authors and Affiliations

  1. N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation

    G. A. Gazieva, V. V. Baranov & A. N. Kravchenko

Authors
  1. G. A. Gazieva
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  2. V. V. Baranov
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  3. A. N. Kravchenko
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Correspondence to G. A. Gazieva.

Additional information

For Part 4, see Ref. 1.

Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1267–1270, June, 2010.

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Gazieva, G.A., Baranov, V.V. & Kravchenko, A.N. 4,5-Dihydroxyimidazolidin-2-ones in α-ureidoalkylation of N-carboxyalkyl-, N-hydroxyalkyl-, and N-aminoalkylureas 5. Synthesis of N-hydroxyalkyl-1,5-diphenylglycolurils. Russ Chem Bull 59, 1296–1299 (2010). https://doi.org/10.1007/s11172-010-0236-7

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  • DOI: https://doi.org/10.1007/s11172-010-0236-7

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