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filingDate 1996-08-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e87ddcfb69ffc8d8051be322bbe0a1ab
publicationDate 1997-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2572508-A1
titleOfInvention One pot synthesis of 2-oxazolidinone derivatives
abstract The present invention provides an improved process for preparing (S)-4-{[3-[2-(dimethylamino)ethyl)-1H-indol-5-yl]methyl}-2-oxazolidinone which comprises: a) forming a carbamate of formula (III), from methyl 4-nitro-(L)-phenylalaninate hydrochloride; b) reducing the compound of formula (III) to give the compound of formula (IV); c) reducing the methyl ester grouping in the compound of formula (IV) to give the compound of formula (V); d) ring closure of the compound of formula (V) to give the compound of formula (VI); e) diazonium salt formation from the compound of formula (VI) followed by reduction to give the compound of formula (VII); f) Fischer reaction of the compound of formula (VII) to give (S)-4-{[3-[2-(dimethylamino)ethyl]-1H-indol-5-yl]methyl)-2-oxazolidinone.
priorityDate 1995-08-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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