Chemistry of Heterocyclic Compounds

, Volume 23, Issue 4, pp 435–439 | Cite as

Study of products of reaction of diaroylethylenes with o-phenylenediamine and 1,3-dimethyl-5,6-diaminouracil

  • V. D. Orlov
  • S. M. Desenko
  • B. Insuasti
  • K. A. Potekhin
  • Yu. T. Struchkov
Article
  • 30 Downloads

Abstract

It was shown that the product of the reaction of dibenzoylethylene with o-phenyl enediamine has the structure of 2-phenacyl-3-phenyl-1,2-dihydroquinoxaline. The steric structure of the dihydroqyinoxaline bicyclic compound was discussed. It was shown that the reaction of di(4-toluyl)ethylene with 1,3-dimethyl-5,6-diaminouracil leads to 5,7-dimethyl-6,8-dioxo-2-(4-methylphenacylidene)-3-(4-tolyl)-1,2-dihydropyrimidino[5,6-b]pyrazine.

Keywords

Ethylene Organic Chemistry Pyrazine Steric Structure Enediamine 

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Copyright information

© Plenum Publishing Corporation 1987

Authors and Affiliations

  • V. D. Orlov
    • 1
    • 2
    • 3
  • S. M. Desenko
    • 1
    • 2
    • 3
  • B. Insuasti
    • 1
    • 2
    • 3
  • K. A. Potekhin
    • 1
    • 2
    • 3
  • Yu. T. Struchkov
    • 1
    • 2
    • 3
  1. 1.A. M. Gor'kii Kharkov State UniversityKhar'kov
  2. 2.A. N. Nesmeyanov Institute of Heteroorganic CompoundsMoscow
  3. 3.P. I. Lebedev-Polyanskii Vladimir State Pedagogical InstituteVladimir

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