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Chemistry of oxalyl derivatives of methyl ketones. XLVI. Reaction of. beta. -bromoaroylpyruvic esters with urea

Journal Article · · J. Org. Chem. USSR (Engl. Transl.); (United States)
OSTI ID:6974762

The substitution of the bromine atom in methyl ..beta..-bromoaroylpyruvates by urea is accompanied by cyclization of the substitution product. Depending on the reaction conditions, this leads either to 6-aroyl-5-hydroxyuracils or to 5-aryl-4-methoxycarbonyl-2,3-dihydro-2-imidazolones. The UV spectra were recorded on a Specord UV-Vis spectrometer in ethanol with the substances at concentrations of 10/sup -4/-10/sup -5/ M. The IR spectra were recorded in Vaseline oil on a UR-20 spectrometer. The PMR spectra were recorded in deuteroacetone on an RS-60 spectrometer with HMDS as internal standard. The mass spectra were recorded on a Varian Mat-311 spectrometer at 70 eV.

Research Organization:
Perm Pharmaceutical Institute (USSR)
OSTI ID:
6974762
Journal Information:
J. Org. Chem. USSR (Engl. Transl.); (United States), Journal Name: J. Org. Chem. USSR (Engl. Transl.); (United States) Vol. 23:4; ISSN JOCYA
Country of Publication:
United States
Language:
English

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