http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20070000508-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_27a71ddaaa2f5a8c228fc6cb3f3b3098
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-167
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-43
filingDate 2005-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b911e34b85fdef0b784f6a67a75eeae2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4e84427345538dfc7600822880761fb1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5dd3f3b3c9858efed22aa9089504096b
publicationDate 2007-01-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20070000508-A
titleOfInvention Chemical process and new crystalline form
abstract The present invention relates to the preparation of β 2 -adrenoreceptor agonists in crystalline form. In particular, the present invention relates to the preparation of crystalline salts of compounds of formula (I), in particular crystalline monohydrochloride salts. The present invention relates to novel crystalline forms (polymorphs) of the monohydrochloride salts of compounds of formula (la) and methods of preparing them.
priorityDate 2004-04-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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