http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105061295-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-76
filingDate 2015-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_06fe09c7972d21eb58154ebe78fe8ae5
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publicationDate 2015-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105061295-A
titleOfInvention Synthetic method for lurasidone precursor compound (3AR,4S,7R,7AS) 4,7-methylene-1H-isoindole-1,3(2H)-diketone
abstract The present invention relates to the chemical field, and discloses a synthetic method for a lurasidone precursor compound (3AR,4S,7R,7AS) 4,7-methylene-1H-isoindole-1,3(2H)-diketone. According to the present invention, a compound (reference to the specification) is used to synthesize the lurasidone precursor compound (3AR,4S,7R,7AS) 4,7-methylene-1H-isoindole-1,3(2H)-diketone by inversion of configuration at the temperature of 170-180 DEG C, and a yield of the lurasidone precursor compound (3AR,4S,7R,7AS) 4,7-methylene-1H-isoindole-1,3(2H)-diketone can reach 90%; and in a reaction for preparing the compound (reference to the specification), the operation is simple, the reaction time is short, and a yield can reach 98%; and in a whole synthesis route that takes dicyclopentadiene as an initiator, a noble catalyst and a reagent with great environmental contamination are not used, so that the whole synthetic process is not only light in pollution, easy in treatment, but also has a lowest yield of 90% in each step; and the total yield can be about 83.8%.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114685349-A
priorityDate 2015-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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