http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-200536814-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/A61K31-167
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-167
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filingDate 2005-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4e84427345538dfc7600822880761fb1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5dd3f3b3c9858efed22aa9089504096b
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publicationDate 2005-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-200536814-A
titleOfInvention Chemical process and new crystalline form
abstract The present invention relates to the preparation of a β2 adrenergic agonist in crystalline salt form. In particular the invention relates to preparation of a crystalline salt of compound (I), in particular a crystalline monohydrochloride salt. The invention also relates to a new crystalline form (polymorph) of the monohydrochloride salt of compound (Ia) and a process for preparing it.
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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