http://rdf.ncbi.nlm.nih.gov/pubchem/patent/NZ-524363-A

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filingDate 2001-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f2d49c64d1421d218136e4862c540d2a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_acc60f530a5440ed7d8c07ddaf0d42ac
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publicationDate 2004-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber NZ-524363-A
titleOfInvention Processes for preparing cilostazol (6-[4-(1-cyclohexyl- 1H-tetrazol-5-yl)butoxy]-3,4-dihydro-2(1H)-quinolinone)
abstract Processes for preparing 6-[4-(1-cyclohexyl-1H-tetrazol- 5-yl)butoxy]-3,4-dihydro-2(1H-quinolinone of formula (I) which is also known by the generic name cilostazol are disclosed, wherein a process for preparing cilostazol of formula (I) comprises: (a) dissolving 6-hydroxy-3,4-dihydroquinolinone and a water- soluble base in water to form an aqueous phase, (b) dissolving a 1-cyclohexyl-5-(4-halobutyl)-tetrazole in a water-immiscible solvent to form an organic phase, (c) forming a biphasic mixture by contacting the aqueous phase and the organic phase in the presence of a quaternary ammonium phase transfer catalyst, (d) and recovering cilostazol from the biphasic mixture. Cilostazol inhibits cell platelet aggregation and is used to treat patients with intermittent claudication.
priorityDate 2000-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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