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grantDate 2014-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 2014-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2453970-T3
titleOfInvention Procedures for the resolution of the mixture of optical isomers, especially pinocembrin racemate
abstract A method for the resolution of a mixture of optical isomers of pinocembrina, in particular a racemate of pinocembrina, said procedure comprising the following steps: (1) carrying out a derivatization reaction of a mixture of optical isomers of pinocembrina, which has been subjected to a protection of the phenolic hydroxyl group, with a chiral primary amine to provide a mixture of diastereoisomers, and carry out a separation of the mixture of diastereoisomers and optionally carry out a purification; and (2) desderivatize the separated diastereoisomers, and carry out a deprotection, and optionally carry out a purification, to obtain (R) - (+) - pinocembrina and / or (S) - (-) - pinocembrina, in the that said chiral primary amine is represented by the following general formula: chiral primary amine wherein, R1 is selected from -H, -CH3, -CH2CH3, -CH2CH2CH3, -CH (CH3) 2 or -CH2OH; R2 is selected from phenyl, benzyl, or phenyl or benzyl with a substituent on an aromatic ring thereof, -CH2OH-CH (OH) CH3, -CH (OH) C2H5, phCH (OH) - in which the substituent is selected of -CH3, -CH2CH3, -CH2CH2CH3, - (CH2) 3CH3, -CH (CH3) 2, -NO2, -CF3, -F, -CI, -I, -OH, -OCH3, -OC2H5, -COOCH3, -COOC2H5, -CONH2, -CONHCH3, -CONHC2H5, -CON (CH3) 2 or -CONHCH (CH3) 2; R3 has the same definition as that of R1 and R2 with the proviso that R3 does not have the same structure as R1 or R2 at the same time.
priorityDate 2007-11-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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