FIELD: organic chemistry, chemical technology. SUBSTANCE: invention relates to method for preparing 5-[4-[[3-methyl-4-oxo-3,4-dihydroquinazoline-2-yl] methoxy] benzyl] -thiazolidine-2,4-dione of the formula (I) . Method involves reduction of compound of the formula (2') wherein R means (C1-C4) alkyl group using Raney nickel or magnesium and if necessary the repeated esterification using sulfuric acid in the range of temperature from 0C to 60 C to yield compound of the formula (3') that is subjected for hydrolysis to yield acid of the formula (4) followed by condensation of acid of the formula (4) with N-methylanthranylamide of the formula (7) without any preliminary activation of acid to yield compound of the formula (I) that if necessary is converted to pharmaceutically acceptable salt. Invention relates also to method for preparing compound of the formula (2') involving interaction of p-hydroxybenzaldehyde of the formula (10) with alkylhaloacetate of the formula (11) wherein Hal means halogen atom and R means (C1-C4)-alkyl in the presence of aromatic hydrocarbon solvent, base, alkylor arylsulfonic acid and iodine to yield compound of the formula (12) that is subjected for condensation with thiazolidine-2,4-dione of the formula (13) in the presence of absence of a solvent and using catalyst to yield compound of the formula (2'). EFFECT: improved preparing method of derivatives of thiazolidine-2,4-dione. 36 cl, 40 ex
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Authors
Dates
2004-02-20—Published
1999-09-10—Filed