http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002531450-A
Outgoing Links
Predicate | Object |
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classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-16 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4525 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-24 |
filingDate | 1999-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 2002-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-2002531450-A |
titleOfInvention | Process for producing paroxetine hydrochloride |
abstract | (57) [Summary]nBy crystallizing from a solution of paroxetine hydrochloride in propan-2-ol to which a crystal habit modifier compound has been added, crystalline paroxetine having a modified crystal habit that more easily desolvates to form an anhydride. A hydrochloride / propan-2-ol solvate is obtained. Heating a crystalline solvate having a modified crystal habit in a vacuum oven gives Form A anhydride. Suitable crystal habit modifiers are carboxylic acids and amine salts. |
priorityDate | 1998-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 32.