http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1549639-A1
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_27a71ddaaa2f5a8c228fc6cb3f3b3098 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-30 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-12 |
filingDate | 2003-10-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_368f0cdf7facaaf5c1d845b0d4f9b1cb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_669c2ab004a282b38c96ad36b0f3db18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5ed98fdd875773297a6fa9a8f57ccd9f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8b54bd99abec2ba61718f551c56f2084 |
publicationDate | 2005-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | EP-1549639-A1 |
titleOfInvention | Sulphonamide derivatives as antipsychotic agents |
abstract | The invention provides compounds of formula (I): wherein A and B represent the groups -(CH<SUB>2</SUB>)<SUB>m</SUB>- and -(CH<SUB>2</SUB>)<SUB>n</SUB>- respectively; R<SUP>1 </SUP>represents hydrogen or C<SUB>1-6</SUB>alkyl; R<SUP>2 </SUP>represents hydrogen, halogen, hydroxy, cyano, nitro, hydroxyC<SUB>1-6</SUB>alkyl, trifluoromethyl, trifluoromethoxy, C<SUB>1-6</SUB>alkyl, C<SUB>1-6</SUB>alkoxy, C<SUB>1-6</SUB>fluoroalkoxy, -(CH<SUB>2</SUB>)<SUB>p</SUB>C<SUB>3-6</SUB>cycloalkyl, -(CH<SUB>2</SUB>)<SUB>p</SUB>OC<SUB>3-6</SUB>cycloalkyl, -COC<SUB>1-6</SUB>alkyl, -SO<SUB>2</SUB>C<SUB>1-6</SUB>alkyl, -SOC<SUB>1-6</SUB>alkyl, -S-C<SUB>1-6</SUB>alkyl, -CO<SUB>2</SUB>C<SUB>1-6</SUB>alkyl, -CO<SUB>2</SUB>NR<SUP>5</SUP>R<SUP>6</SUP>, -SO<SUB>2</SUB>NR<SUP>5</SUP>R<SUP>6</SUP>, -(CH<SUB>2</SUB>)NR<SUP>5</SUP>R<SUP>6</SUP>, -(CH<SUB>2</SUB>)<SUB>p</SUB>NR<SUP>5</SUP>COR<SUP>6</SUP>, optionally substituted aryl ring, optionally substituted heteroaryl ring or optionally substituted heterocyclyl ring; R<SUP>3 </SUP>represents hydrogen, halogen, hydroxy, cyano, nitro, hydroxyC<SUB>1-6</SUB>alkyl, trifluoromethyl, trifluoromethoxy, C<SUB>1-6</SUB>alkyl, C<SUB>1-6</SUB>alkoxy, C<SUB>1-6</SUB>fluoroalkoxy, -(CH<SUB>2</SUB>)<SUB>p</SUB>C<SUB>3-6</SUB>cycloalkyl, -(CH<SUB>2</SUB>)<SUB>p</SUB>OC<SUB>3-6</SUB>cycloalkyl, -COC<SUB>1-6</SUB>alkyl, -SO<SUB>2</SUB>C<SUB>1-6</SUB>alkyl, -SOC<SUB>1-6</SUB>alkyl, -S-C<SUB>1-6</SUB>alkyl, -CO<SUB>2</SUB>C<SUB>1-6</SUB>alkyl, -CO<SUB>2</SUB>NR<SUP>7</SUP>R<SUP>8</SUP>, -SO<SUB>2</SUB>NR<SUP>7</SUP>R<SUP>8</SUP>, -(CH<SUB>2</SUB>)<SUB>p</SUB>NR<SUP>7</SUP>R<SUP>8 </SUP>or -(CH<SUB>2</SUB>)<SUB>p</SUB>NR<SUP>7</SUP>COR<SUP>8</SUP>; R<SUP>4</SUP>represents hydrogen, hydroxy, C<SUB>1-6</SUB>alkyl, C<SUB>1-6</SUB>alkoxy, C<SUB>1-6</SUB>fluoroalkoxy, trifluoromethyl, trifluoromethoxy, halogen, -OSO<SUB>2</SUB>CF<SUB>3</SUB>, -(CH<SUB>2</SUB>)<SUB>p</SUB>C<SUB>3-6</SUB>cycloalkyl, -(CH<SUB>2</SUB>)<SUB>q</SUB>OC<SUB>1-6</SUB>alkyl or -(CH<SUB>2</SUB>)<SUB>p</SUB>OC<SUB>3-6</SUB>cycloalkyl; R<SUP>5 </SUP>and R<SUP>6 </SUP>each independently represent hydrogen, C<SUB>1-6</SUB>alkyl or, together with the nitrogen or other atoms to which they are attached, form an azacycloalkyl ring or an oxo-substituted azacycloalkyl ring; R<SUP>7 </SUP>and R<SUP>8 </SUP>each independently represent hydrogen or C<SUB>1-6</SUB>alkyl; m and n independently represent an integer selected from 1 and 2; p independently represents an integer selected from 0, 1, 2 and 3; q independently represents an integer selected from 1, 2 and 3; or a pharmaceutically acceptable salt or solvate thereof, with the proviso that the compounds 8-hydroxy-3-methyl-7-phenylsulfonyl-2,3,4,5-tetrahydro-1H-3-benzazepine, 8-hydroxy-7-4-(hydroxyphenyl)sulfonyl-2,3,4,5-tetrahydro-1H-3-benzazepine, 7-phenylsulfonyl-1,2,3,4-tetrahydroisoquinoline and 7-phenylsulfonyl-1,2,3,4-tetrahydroisoquinoline hydrochloride are excluded. The compounds are useful in therapy, in particular as antipsychotic agents. |
priorityDate | 2002-10-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 264.