http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2004323810-B2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-18
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filingDate 2004-10-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_82b3101f638db281e6c39192df025b20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ca203b0ecaf7b6dc69d85b4fc6285928
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7e53b462a7cac8358d322c07a239dc3c
publicationDate 2011-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AU-2004323810-B2
titleOfInvention Novel intermediates useful for the preparation of aripiprazole and methods for the preparation of the novel intermediates and aripiprazole
abstract The invention disclosed in this application relates to an improved process for the preparation of aripiprazole (1) which comprises (i) Reacting 6-hydroxy-l-indanone (11) with 1,4-dihalobutane (12) in the presence of a base and a solvent at a temperature in the range of 90 to 110 deg C to form the novel intermediate 6-(4-halo butoxy)-indan-l-one (3), (ii) reacting the novel intermediate with 1-(2,3-clichlorophenyl)-piperazine (9) to get another novel intermediate 6-[4-[4-(2,3-dichlorophenyl)-l-piperazinyl] butoxy]-indan-l-one (2) and (iii) Reacting the resulting novel compound with sodium azide. The invention also relates to the novel intermediates of the formulae (2) & (3) and processes for their preparation.
priorityDate 2004-10-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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