FIELD: organic chemistry. SUBSTANCE: method involves synthesis of chloroazines containing o-hydroxyphenyl group of the formulas (I) HOC6H4, (II) CH3 and (III) HOC6H4 where Ia - 4-Cl, 2-o-CF3, R - 6-HOC6H4; Ib - 4-Cl, 2-o-C6H5, R - 6-HOC6H4; Ic - 4-Cl, 2-o-HOC6H4, R - 6-COOC2H5; Id - 4-Cl, 2-o-HOC6H4, R - 5-CN; Ie - 4-Cl, 2-o-C6H5, R - 5-o-HOC6H4; If - 4-Cl, 2-o-HOC6H4, R - 5-HOC6H4; Ig -4-Cl, 2-o-HOC6H4, R - H; Ih - 4-Cl, 6-o-C6H5, R - H; Ii - 4-Cl, 2-o-OC3H7, R - H; Ij - 4-Cl, 4-o-NO2, R - 6-; IIa - R - H; IIb - R - 4-; IIc - R - 5-Br; IId - R - 5-; IIe - R - 3,5-Cl; IIIa - R - H. Reagent 1: (o-hydroxyphenyl)-dihydroazinones. Reagent 2: chloroanhydrides of organic or inorganic acids (phosphoryl chloride, phosphorus trichloride, thionyl chloride, cyanurchloride, phosphorus pentachloride). Process is carried out in the medium of dimethylformamide at molar ratio of reagents 1:2. Synthesized compounds are used in medicinal industry. EFFECT: improved method of synthesis. 2 cl
Authors
Dates
1995-01-09—Published
1991-06-18—Filed