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filingDate 2002-08-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2005-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0e7351ebeb073ca1b2957c6797a24a8b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0673124e0e71c06e9a50b4a1f7e23077
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publicationDate 2005-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-6852858-B2
titleOfInvention Process for purifying N-[3-(3-cyanopyrazolo[1,5-a]pyrimidin-7-yl)phenyl]-N-ethylacetamide (zaleplon) and crystalline forms of zaleplon accessible with the process
abstract Zaleplon can be separated from a regioisomer impurity by crystallization from selected solvents or by adding an anti-solvent to a solution of zaleplon and the regioisomer. Zaleplon crystalline Forms II, III, IV, and V are useful for the treatment of insomnia. These crystalline Forms are described along with processes for making them v crystallization from selected solvents.
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