http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2479932-A1

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filingDate 2003-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f201f57717123d5598b83ab6b8f60148
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publicationDate 2003-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2479932-A1
titleOfInvention Piperazine substituted aryl benzodiazepines and their use as dopamine receptor antagonists for the treatment of psychotic disorders
abstract Described herein are antipyschotic compounds of formula (I) wherein, A is an optionally benzo-fused five or six member aromatic ring having zero to three hetero atoms independently selected from N, O, and S; Alk is (C1-4) alkylene optionally substituted with OH, methoxy, ethoxy, or F; Ar is optionally substituted phenyl, naphthyl, monocyclic heteroaromatic, or bicyclic heteroaromatic; R1 is hydrogen or (C1-4) alkyl optionally substituted with OH, OR3, or OCH2CH2OH, wherein R3 is (C1-2) alkyl; R2 is H, (C1-6) alkyl, halogen, fluorinated (C1-6) alkyl, OR4, SR4, NO2, CN, COR4, CONR5R6, SO2NR5R6, NR5R6, NR5COR4, NR5SO2R4, or optionally substituted phenyl,wherein R4 is hydrogen, (C1-6) alkyl, fluorinated (C1-6) alkyl, benzyl, or optionally substituted phenyl, R5 and R6 are independently hydrogen, (C1-6) alkyl, or optionally substituted phenyl; Z is one or two substituents independently selected from hydrogen, halogen, (C1-6) alkyl, fluorinated (C1-6) alkyl, OR7, SR7, NO2, CN, COR7, CONR8R9, SO2NR8R9, NR8SO2R7, NR8R9, or optionally substituted phenyl, wherein R7 is hydrogen, (C1-6) alkyl, fluorinated (C1-6) alkyl, benzyl, or optionally substituted phenyl, R8 and R9 are independently hydrogen, (C1-6) alkyl, or optionally substituted phenyl; and salts, solvates, and crystal forms thereof. Also described are the use of the compounds of formula (I) as antagonists of the dopamine D2 receptor and as agents for the treatment of psychosis and bipolar disorders, and pharmaceutical formulations of the compounds of formula (I). Also described are compounds useful as intermediates for the synthesis of the compounds of formula (I).
priorityDate 2002-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424045826
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426243886
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419544741
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415764924
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424045831
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457798390
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID67993
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21093461
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID136005534
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394780
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414543499
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID407206081
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424045832
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21966342
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412012943
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID448233682
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414540246
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID451623347
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394753
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21093479
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21822800
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415737714
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID451541399
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419589026
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID448878560
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414540247
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11575
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8029
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419539003
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID13654641
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID416749923
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Total number of triples: 682.