http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007505076-A

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filingDate 2004-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2007-03-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2007505076-A
titleOfInvention 7-heteroarylsulfonyl-tetrahydro-3-benzazepine derivatives as antipsychotic agents
abstract The present invention relates to a compound of formula (I) [Wherein, A and B represent — (CH 2 ) m — and — (CH 2 ) n — groups, respectively; R 1 represents hydrogen or C 1-6 alkyl; R 2 represents hydrogen, Halogen, hydroxy, cyano, nitro, hydroxy C 1-6 alkyl, trifluoromethyl, trifluoromethoxy, C 1-6 alkyl, C 1-6 alkoxy, C 1-6 fluoroalkoxy, — (CH 2 ) p C 3 -6 cycloalkyl, - (CH 2) p OC 3-6 cycloalkyl, -COC 1-6 alkyl, -SO 2 C 1-6 alkyl, -SOC 1-6 alkyl, -S-C 1-6 alkyl, —CO 2 C 1-6 alkyl, —CO 2 NR 3 R 4 , —SO 2 NR 3 R 4 , — (CH 2 ) p NR 3 R 4 , — (CH 2 ) p NR 3 COR 4 , substituted May Reel ring, optionally substituted heteroaryl ring, fused bicyclic represents an aromatic heterocyclic ring system or heterocyclic ring which may be substituted; Ar 1 represents a heteroaryl ring which may be substituted; Ar 2 represents an optionally substituted aryl ring or an optionally substituted heteroaryl ring; Z represents — (CH 2 ) q X— (wherein the — (CH 2 ) q — group represents Ar 2 ) or —X (CH 2 ) q — (wherein X is bonded to Ar 2 ), wherein any of the —CH 2 — groups is one or more C Optionally substituted by a 1-6 alkyl group; X represents oxygen, —CH (OR 5 ) —, —NR 5 — or —CH 2 —, wherein the —CH 2 — group is one or more It may be substituted by C 1-6 alkyl group; R 3 and Each 4, independently, hydrogen, C 1-6 represents an alkyl, or they taken together with the nitrogen or other atoms are bonded, azacycloalkyl ring or an oxo-substituted azacycloalkyl ring R 5 represents hydrogen or C 1-6 alkyl; m and n independently represent an integer selected from 1 and 2; p independently represents 0, 1, 2 And q independently represents an integer selected from 0, 1, 2 and 3; provided that Ar 1 is a pyridyl group and Z is —CH 2 X— ( Wherein X is bound to the Ar 1 group), X is selected from —CH (OR 5 ) —, —NR 5 — and —CH 2 —, wherein the —CH 2 — The group may be substituted by one or more C 1-6 alkyl groups] Or a pharmaceutically acceptable salt or solvate thereof. The compounds of formula (I) are useful in therapy, in particular as antipsychotic agents.
priorityDate 2003-09-12-04:00^^<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/SID419545319
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10422
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457635959
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419492817
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID24693
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424930913
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID16363
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419492792
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426248706
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID25137853
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419549422
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID941651
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID16362
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419492701
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419540210
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410111933
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2662
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9842523
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4744
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID452187582
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23663956
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419585920
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID451268575
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID66707141
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419507641
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4917
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID444
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21941165
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Total number of triples: 359.