http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H09221603-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B11-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B41M5-327
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B41M5-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B67-48
filingDate 1996-02-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2cc51b40d2f7242bf2dd6aef2a0cc596
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_313b5f0ad2600d98f925bbea073f997d
publicationDate 1997-08-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H09221603-A
titleOfInvention Process for producing low-melting type 2-anilino-3-methyl-6- (N-ethyl-N-isopentylamino) fluorane
abstract (57) [Summary] (Modified) SOLUTION: 2- (4 ′-(N-ethyl-N-isopentylamino) -2′-pydoxybenzoyl) benzoic acid and 4-methoxy-2-methyldiphenylamine Phthalide obtained by reacting with and in concentrated sulfuric acid is subjected to a ring closure reaction in a mixed solution of an organic solvent and an alkali hydroxide aqueous solution, and then an organic solvent layer containing fluorane obtained by this ring closure reaction is separated from an aqueous layer. After that, if necessary, this organic solvent layer is heated to completely dissolve fluorane in the organic solvent, and then the organic solvent layer is cooled to precipitate crystals, which is a low melting point type 2. -Process for producing anilino-3-methyl-6- (N-ethyl-N-isopentylamino) fluorane. [Effect] It is possible to provide a target substance which is reproducibly and substantially consists of α-form.
priorityDate 1996-02-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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