FIELD: chemistry.
SUBSTANCE: invention relates to a method for synthesis of (-)-3-(4-(2,4-difluorobenzyloxy)-3-bromo-6-methyl-2-oxopyridin-1(2H)-yl)-N,4-dimethylbenzamide or a pharmaceutically acceptable salt thereof, involving the following steps: a) bringing compounds of formula V into contact with a brominating agent in the presence of at least one solvent to obtain a compound of formula IV, b) bringing the formula IV compound into contact with hydrolase in the presence of a buffer solution to obtain a compound of formula X, c) bringing the formula X compound into contact with an activating reagent in the presence of at least one solvent and then bringing the obtained mixture into contact with methylamine to obtain a compound of formula IX, d) bringing the formula IX compound into contact with 2,4-diflluorobenzylhalide in the presence of a base and at least one solvent; where the compounds V, IV, IV, X and IX are as described in the claim. The invention also relates to novel compounds, specifically to methyl-3-(3-bromo-4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-4-methylbenzoate, (-)-3-(3-bromo-4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-4-methylbenzoic acid and (-)-3-(3 -bromo-4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-N,4-dimethylbenzamide.
EFFECT: described is a novel method for synthesis of (-)-3-(4-(2,4-difluorobenzyloxy)-3-bromo-6-methyl-2-oxopyridin-1(2H)-yl)-N,4-dimethylbenzamide, which avoids several time-consuming operations, for example multiple extractions, and also avoids use of expensive materials.
12 cl, 2 ex
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Authors
Dates
2011-02-10—Published
2007-12-05—Filed