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filingDate 2002-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_606378a54d36309b39ac14bb47db8ec6
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publicationDate 2003-05-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2003083501-A1
titleOfInvention Process for preparing paroxetine HCl which limits formation of pink colored compounds
abstract The present invention provides a process for preparing paroxetine HCl from paroxetine base which provides paroxetine HCl substantially free of pink-colored compounds or an impurity identified by an HPLC RRT of about 1.5. The processes of the present invention utilize a buffer, a molar ratio of HCl to paroxetine base of less than one, and crystallize/recrystallize in the presence of an effective amount of an anti-oxidants. A preferred way to create a buffer is by using ammonium chloride. A preferred anti-oxidant is ascorbic acid. n The present invention also provides for re-crystalizing paroxetine HCl prepared by the above methods or any other methods in the presence of an effective amount of an anti-oxidant such as ascorbic acid. A preferred solvent system for recrystallization is a mixture of acetone and methanol. n Processes of the present invention can combine these various features.
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type http://data.epo.org/linked-data/def/patent/Publication

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