http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2013103794-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C209-56
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filingDate 2011-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2014-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2013103794-A
titleOfInvention NEW METHODS FOR PRODUCING Phenylcyclopropylamine Derivatives AND THEIR APPLICATION FOR PRODUCING TICAGRELOR
abstract 1. A method of obtaining substituted derivatives of phenylcyclopropylamine of the formula II: or their stereochemically isomeric forms, or a mixture of stereochemically isomeric forms, or acid addition salts; where R, R, R, R, and R are each independently selected from a hydrogen atom and a halogen atom, provided that the benzene ring in Formula II is substituted with one or more halogen atoms, where the halogen atom is F, Cl, Br or I; comprising: a) reacting a halogen-substituted benzaldehyde compound of formula VIII: wherein R, R, R, R and R are as defined in formula II; with methyltriphenylphosphonium halide (Wittig reagent) of formula VII: where 'X' is a halogen atom selected from the group consisting of Cl, Br and I; in the presence of a first base in a first solvent to give a substituted styrene compound of formula VI: where R, R, R, R and R are as defined in formula II; b) the reaction of a compound of formula VI with a diazo ester compound of formula V: wherein “R” is an alkyl, cycloalkyl, aryl or aralkyl group; in the presence of a metal catalyst and a chiral ligand in a second solvent to obtain a substituted cyclopropanecarboxylate compound of the formula IV: or a stereochemically isomeric form thereof or a mixture of stereochemically isomeric forms where R, R, R, R, R and R are as defined in formula II; c ) hydrolysis of an ester compound of formula IV with an acid or a second base in a third solvent to obtain a substituted cyclopropanecarboxylic acid compound of formula III: or a stereochemically isomeric form thereof or a mixture of stereo chemically isomeric forms; d) optionally, purification of the compounds tsiklopropank
priorityDate 2010-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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