http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010517968-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-55
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-00
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A23K1-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-55
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00
filingDate 2008-01-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2010-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2010517968-A
titleOfInvention Enantioselective synthesis of 6-amino-7-hydroxy-4,5,6,7-tetrahydro-imidazo [4,5,1-JK] [1] -benzazepin-2 [1H] -one and zilpaterol
abstract The present invention relates to a process for hydrogenating ketoximes to selectively form aminoalcohol stereoisomers, and in particular, 4,5-dihydro-imidazo [4,5,1-jk] [1] benzazepine-2. , 6,7 [1H] -trione-6-oxime or salts thereof to give 6-amino-7-hydroxy-4,5,6,7-tetrahydro-imidazo [4,5,1-jk] [ 1] -Benzazepine-2 [1H] -one relates to a method for selectively forming stereoisomers or salts thereof. The present invention relates to 6-amino-7-hydroxy-4,5,6,7-tetrahydro-imidazo [4,5,1-jk] [1 for the selective production of steric isomers of zilpaterol or salts thereof. It also relates to the use of hydrogenated products of benzoazepine-2 [1H] -one or their salts and the use of such zilpaterol stereoisomers or salts in therapeutic methods and medicine for animals.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112662599-B
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112662599-A
priorityDate 2007-02-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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