http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2553877-C

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0a910d33c239980f3a705e312c5bad6a
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4439
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D-
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-04
filingDate 2005-02-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_99ea5f5f2990617b7246ebe4c025bb6b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a2c8ecefcbb2322726d86848d55577b1
publicationDate 2012-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2553877-C
titleOfInvention Compounds useful for the synthesis of s- and r-omeprazole and a process for their preparation
abstract The present invention relates to an improved method for the synthesis of the (S)- or (R)- enantiomer of omeprazole, characterized in that 2-[[(4-X-3,5-dimethylpyridin-2-yl)methyl]thio]-5-methoxy-1H-benzimidazole or 2-[[(4-X-3,5-dimethyl-1-oxidopyridin-2-yl)methyl]thio]-5-methoxy-1H-benzimidazole, wherein X is a leaving group, is oxidized into the corresponding sulphoxide which is obtained as a crystalline compound. Recrystallisation of the thus obtained sulphoxide results in a compound of enhanced chemical and optical purity, which is subsequently transformed into the (S)- or (R)- enantiomer of omeprazole.
priorityDate 2004-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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