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filingDate 2003-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3462a0836892e005e7291c49bab9a414
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a4965f7b4e75e7c92702b68ed74d9af
publicationDate 2005-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20050039749-A
titleOfInvention Process for preparing rizatriptan
abstract In particular,n n n Preparing a diazonium salt of aniline hydrochloride of formula II, followed by reduction and acidification to obtain hydrazine of formula III (a),n n n Reacting the hydrazine hydrochloride of formula III with α-keto-δ-valerolactone in situ to obtain a hydrazone of formula IV (b),n n n Fischer indole reaction of the hydrazone of formula IV to give pyranoindoleone of formula V, followed by optionally hydrolysis to yield the product of formula VI (c),n n n (D) obtaining a compound of formula VII by transesterifying the compound of formula V or esterifying its hydrolysis product of formula VI, d.n n n Converting the hydroxyl group of the compound of formula VII to dimethylamino to give an indole carboxylate of formula VIII (e),n n n Saponifying a 2-carboalkoxy group of a compound of formula VIII to obtain an indolecarboxylic acid of formula IX; andn n n Decarboxylation of the indolecarboxylic acid of formula (IX) to obtain rizatriptan and pharmaceutically acceptable salts thereof (g), the present invention relates to rizatriptan or a pharmaceutically acceptable method for preparing the same. The invention also relates to synthetic intermediates for obtaining rizatriptan.
priorityDate 2002-08-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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