http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7964749-B2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5f9db723f41b9245df17b048ca637ad2
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C231-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C233-54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D257-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C305-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-31
filingDate 2006-10-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-06-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e3c2d38d8cbcb4e23b5b73e7ffdb21ce
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e80d79d20a3cd9850ffbf2c03388e0b9
publicationDate 2011-06-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7964749-B2
titleOfInvention Process for obtaining valine derivatives useful for obtaining a pharmaceutically active compound
abstract The invention provides a method for obtaining the intermediate (II), useful for manufacturing Valsartan and a drug directed to a treatment of arterial hypertension or heart failure. The process comprises a) Imination of the aldehyde group of a compound (VII) by L-Valine (IV) salts with organic or inorganic bases and a polar solvent or water, where X means halogen or an —OSO2R group, where R is CF3, tolyl, methyl or F; to give an imine-type compound (VIII), where B+ is the protonated form of an organic base or an alkaline cation; b) Reduction of the imine group of the compound (VIII) followed by acidification, to give the compound (VI); and c) N-Acylation of the compound (VI) with valeryl chloride to give the compound (II). Steps a) and b) can be performed in a “one pot” reaction.
priorityDate 2005-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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