FIELD: chemistry.
SUBSTANCE: described is a method of producing (S)-(+)-10,11-dihydro-10-hydroxy-5H-dibenz/b,f/azepine-5-carboxamide or R)-(-)-10,11- dihydro-10-hydroxy-5H-dibenz/b,f/azepine-5-carboxamide by reducing oxcarbazepine in the presence of a catalyst and a hydride source. The catalyst is based on a combination of [RuX2(L)]2, where X is chlorine, bromine or iodine, and L is an acrylic or arylaliphatic ligand, and a ligand of formula
or formula , where values of radicals are given in the claim. The hydride source is either NR3R4R5 and formic acid or [R3R4R5NH][OOCH] and, optionally, formic acid, or [M][OOCH)8 and formic acid, where R3, R4 and R5 denote C1-6-alkyl; M denotes an alkali metal or alkali-earth metal and x equals 1 or 2. During the process, pH is kept between 6.5 and 8. The solvent in which reduction takes place contains at least one polar aprotic solvent.
EFFECT: efficient method of obtaining the compounds.
30 cl, 4 ex, 5 tbl
Title |
Year |
Author |
Number |
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|
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2002 |
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