http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2008012105-A1

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d82de571f8a6ea172282c760db461f54
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-94
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-94
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-517
filingDate 2007-07-25^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2b480fdb46032eb32f603dedf98848bf
publicationDate 2008-01-31^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2008012105-A1
titleOfInvention Crystalline erlotinib
abstract The invention relates to crystalline erlotinib and in particular crystalline erlotinib hydrate. The crystalline erlotinib may be comprised in a pharmaceutical preparation. The crystalline erlotinib may be produced by precipitating from a solution that comprises erlotinib dissolved in a solvent wherein said solvent is selected from methanol, ethanol, isopropanol, acetone, acetonitrile, chloroform, 1,4-dioxane, toluene, and mixtures thereof. The crystalline erlotinib may be used for producing erlotinib salts.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2010005924-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2014118737-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2010109443-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8440823-B2
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2009007984-A3
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8653264-B2
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priorityDate 2006-07-28^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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