http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103896823-A

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filingDate 2012-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_37f4e03f9d32014fad2884510985ff70
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publicationDate 2014-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103896823-A
titleOfInvention Preparation method of intermediate of lurasidone
abstract The invention discloses a preparation method of an intermediate of lurasidone. The preparation method of an intermediate 3 of lurasidone comprises the following steps: (1) subjecting a compound represented by the formula 5 to carry out ammonolysis reactions with one or more components selected from urea, ammonium chloride, and organic acid ammonium in an organic solvent so as to obtain a compound 4; (2) subjecting the compound 4 obtained in the step (1) to carry out reactions with H2 in the presence of a palladium-carbon catalyst so as to obtain the intermediate 3 of lurasidone. The preparation method of an intermediate 4 of lurasidone comprising the following steps: in an organic solvent, subjecting one or more components selected from urea, ammonium chloride, and organic acid ammonium to carry out ammonolysis reactions with a compound represented by the formula 5 so as to obtain the intermediate 4 of lurasidone. The preparation method does not need high temperature or high pressure, and has the advantages of simple preparation technology, high yield, and suitability for amplification production.
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type http://data.epo.org/linked-data/def/patent/Publication

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