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filingDate 2015-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7a93949c302f6286c2f8e9d18c5a0151
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publicationDate 2020-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2748242-T3
titleOfInvention High purity miglustat preparation procedure
abstract A process for the preparation of crystalline miglustat of formula (I) comprising the steps of: ** Formula ** (1) reacting 2,3,4,6-tetra-O-benzyl-1-deoxynojirimycin hydrochloride of formula (V) with n-butyraldehyde and sodium cyanoborohydride in an organic solvent to prepare 2,3,4,6-tetra-O-benzyl-N-butyl-1-deoxynojirimycin hydrochloride of formula (VI); ** Formula ** (2) react 2,3,4,6-tetra-O-benzyl-N-butyl-1-deoxynojirimycin hydrochloride of formula (VI) with hydrogen in the presence of 10% Pd / C and HCl to producing the hydrochloric salt of miglustat of formula (III); ** Formula ** (3) dissolving the hydrochloric salt of miglustat of formula (III) in a first solvent and adding an organic base; (4) optionally removing the first solvent, and (5) adding a second solvent to crystallize miglustat of formula (I); wherein none of steps (1) to (5) involve the use of any flash column or ion exchange column chromatography.
priorityDate 2014-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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