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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_dfd617dc43a4c986d2dd81e4cb39d9dd
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C257-18
filingDate 1997-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3a4c61f3d7ca8d2901c88b81105cb8fe
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5587ef0fa8513c150f45fea5fb69d90a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_67ff6f5c93ec61da9af11215ccf6f42d
publicationDate 1999-07-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H11193265-A
titleOfInvention Salt of 3- (7-amidino-2-naphthyl) -2-phenylpropionic acid derivative
abstract PROBLEM TO BE SOLVED: To provide an aromatic amidine derivative having an anticoagulant activity based on an excellent activated blood coagulation factor X inhibitory activity (Japanese Patent Application Laid-Open No. 5-208946 and International Publication WO96 / No. 16940), thereby providing an intermediate salt An industrial process for producing the above-mentioned aromatic amidine derivative is provided. SOLUTION: General formula (A) By using a salt formed by the compound represented by and benzoic acid, the above-mentioned aromatic amidine derivative can be produced simply and inexpensively without performing complicated resin purification using a synthetic adsorption resin, and at a high purity. be able to.
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priorityDate 1997-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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