http://rdf.ncbi.nlm.nih.gov/pubchem/patent/NZ-509243-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_27155ed29f9b0bfa281f4b21b26d709a
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D455-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P17-14
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D455-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D455-02
filingDate 1999-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fa4c6cf0c6168efa2f755ee7febe4e26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_235a81fde512dd2077ebad0e87cf4764
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publicationDate 2002-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber NZ-509243-A
titleOfInvention Process for the synthesis of (1H)-benzo[C]quinolizin-3-ones derivatives
abstract A process for the preparation of (1H)-benzo[c]quinolizin-3-ones derivatives of formula (I), where: R1, R2, R3, R4, R5, same or different, are H, alkyl, alkenyl, alkinyl, cycloalkyl, aryl, heterocycle, halogen, CN, azide, NRR', alkylamino, alkyloxy, COOR or CONRR' where R and R', same or different are H, alkyl, cycloalkyl, aryl, heterocycle or arylalkyl; Q is a bond, alkyl, alkenyl, alkinyl, cycloalkyl, CO, CONR or NR; W is H, trifluoromethyl, alkoxy, alkoxyalkyl, arylalkyl, aryloxy, arylamino, alkylcarbonyl, arylcarbonyl, arylcarboxyl, arylcarboxyamide, halogen, CN, azide, NRR' alkylamino or optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, aryl or heterocycle. n is 1 to 4 The compounds of formula (I) are useful as inhibitors of 5รก-reductases.
priorityDate 1998-08-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 22.