http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2289945-B1

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filingDate 2006-07-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2008-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bcf777f08d1f73a604bea2e1d88cb738
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ed089bc823eef0a8e41b2361cce55570
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publicationDate 2008-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2289945-B1
titleOfInvention PROCEDURE FOR OBTAINING TWO ADVANCED INTERMEDIATES AND ITS USE FOR OBTAINING ATORVASTATIN CALCICA AMORFA.
abstract Procedure for obtaining twonAdvanced intermediates and their use for obtaining atorvastatinnCalcium amorphous.n n n The present invention provides a process for obtaining 2- {6- (4R, 6R) - {2- [3-phenyl-4-phenylcarbamoyl-2- (4-fluorophenyl) -5-isopropylpyrrol-1-yl] ethyl } -2,2-dimethyl-1,3- dioxan-4-yl} tert-butyl acetate and 6- (4R, 6R) - {2- [3-phenyl-4-phenylcarbamoyl-2- (4-fluorophenyl) -5-isopropylpyrrol-1-yl] ethyl} tetrahydro-4-hydroxypyran-2-one, key intermediates in the preparation of calcium atorvastatin. The procedure consists in reacting 2-phenyl-1- (4-fluorophenyl) ethanone with 1-bromo-3-methyl-2-butanone under atmosphere inert and in the presence of a strong base, then react the resulting compound (±) -2-phenyl-1- (4-fluorophenyl) -5-methylhexan-1,4-dione with 2 - [(4R, 6R) -6- (2-aminoethyl) -2,2-dimethyl-1,3-dioxan-4-yl] tert-acetate butyl at reflux of toluene and heptane in the presence of an acid catalyst to obtain {6- (4R, 6R) - {2- [3-phenyl-2- (4-fluorophenyl) -5-isopropylpyrrol-1-yl] ethyl} -2,2-dimethyl-1,3-dio- xan-4-yl} tert-butyl acetate, a new intermediate from which, after various stages of synthesis that include halogenation with a halosuccinimide and carbonylation with carbon monoxide in the presence of aniline, said advanced intermediates are obtained for obtaining atorvastatin calcium. The use of these intermediates to obtain calcium atorvastatin is also provided. amorphous after a series of stages of hydrolysis, sodium salt formation and isolation of amorphous raw calcium atorvastatin, which is purified to obtain a high quality product.
priorityDate 2006-07-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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