http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2015042683-A

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-4164
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-68
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4174
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-70
filingDate 2014-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_57c4997c238faadea7372cb28b1fd88e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4995a1ad023c3486ff4733940c4a4ec4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fbf34ca37b1012fce516418b53b51eeb
publicationDate 2015-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2015042683-A
titleOfInvention Method for preparing biphenylimidazole compound
abstract The present invention provides a process for preparing intermediates useful in the preparation of compounds of formula (IV) or salts thereof. The present invention provides a process for preparing intermediates that are useful in the preparation of compounds of formula (IV) or salts thereof. Here, in the formula, R1 to R3 are as defined in the present specification. In one embodiment, the process further comprises preparing a crystalline form of the compound of formula II. One embodiment of the present invention relates to crystalline 4 '-(5-aminomethyl-2-ethoxy-4-ethylimidazol-1-ylmethyl) -3'-fluorobiphenyl-2-carboxylic acid t-butyl ester. [Selection figure] None
priorityDate 2009-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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