http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101149821-B1

Outgoing Links

Predicate Object
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P13-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4412
filingDate 2010-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2012-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-101149821-B1
titleOfInvention New Preparation Method of Diphenyl Acetate Derivatives
abstract The present invention provides a safe and efficient method for preparing propiberine hydrochloride of formula (I), which is an agent for the prevention and treatment of urinary incontinence and urinary incontinence caused by irritable bladder diseases such as neurological bladder disease, neuroanguria disease, unstable bladder disease, chronic cystitis and chronic prostatitis. In more detail, 2-halo-2, 2-diphenylacetate derivatives are prepared from commercially available diphenylacetate derivatives, and substituted with 1-propanol to produce diphenylpropoxy acetic acid esters. After the transesterification reaction with 4-hydroxy-N-methylpiperidine to provide a high-purity propiberine hydrochloride to provide a novel production method that is safer than the existing method and low production cost. [Formula 1]
priorityDate 2010-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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