FIELD: chemistry.
SUBSTANCE: method involves 1) dividing a racemate into two pure enantiomers via chromatographic separation on a chiral polysaccharide as a stationary phase with alcohol as the mobile phase and sorption of the eutomer, 2) repeated racemisation of the distomer with a base using a catalyst in a solvent selected from ether or a mixture of solvents containing ether, at temperature between 80°C and 120°C and 3) subjecting the obtained racemate to separation at step 1) in a repeated cycle. The invention also pertains to use of a pure S-enantiomeric form of a formula I compound, particularly (-)-(S)-N-(1-cyano-2-(5-cyano-2-trifluoromethylphenoxy)-1-methylethyl)-4-trifluoromethylsulfanylbenzamide, for control of entozoic parasites of warm-blooded animals, such as helminths.
EFFECT: efficient method of producing a unique enantiomer from a racemate of amidoacetonitrile compound having a formula in which R1, R2 and R3 independently denote cyano, halo-C1-C6alkyl or halo-C1-C6alkylthio.
15 cl, 1 ex
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Authors
Dates
2011-01-10—Published
2005-11-07—Filed