http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2005176724-A1

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filingDate 2003-02-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5eb28d8fd06f817fa3767291846041e2
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publicationDate 2005-08-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2005176724-A1
titleOfInvention Piperidine and piperazine derivatives possessing affinity at 5ht-1 type receptors
abstract Compounds of formula (I) and pharmaceutically acceptable salts thereof are disclosed: n n nwherein A is optionally substituted phenyl, indolyl, quinolinyl, quinazolinyl, indazolyl or isoquinolinyl; X is carbon, Y is CH and ═ is a double bond; or X is CH, Y is CH 2 or oxygen and ═ is a single bond; or X is nitrogen, Y is CH 2 and ═ is a single bond; R 1 is halogen, cyano, nitro, C 1-6 alkyl, haloC 1-6 alkyl, C 1-6 alkoxy, C 3-7 heterocyclylC 1-6 alkyl, C 3-7 heterocyclyl C 1-6 alkoxy; a is 0, 1, 2, 3 or 4; R2 is either: halogen, —CN, an optionally substituted C 3-7 cycloalkyl, an optionally substituted aryl or an optionally substituted C-linked 3-7 membered heterocyclic group; or a group -(Z)b-B wherein: (i) Z is oxygen, CH 2 , C═O, SO 2 or C═N—OR3 wherein R3 is hydrogen or C 1-6 alkyl; b is 1, 2, or 3; and B is hydrogen, C 1-6 alkyl, C 3-7 cycloalkyl, C 1-6 alkoxy or NR4R5 wherein R4 and R5 are independently hydrogen, C 1-6 alkyl, C 3-7 cycloalkyl, C 1-6 alkanoyl, fluoroC 1-6 alkanoyl, C 1-6 alkylsulfonyl, fluoroC 1-6 alkylsulfonyl, carbamoyl or C 1-6 alkylcarbamoyl, or R4 and R5, together with the nitrogen atom to which they are attached, form part of an optionally substituted 3 to 7 membered heterocyclic group; or (ii) Z is oxygen, CH or CH 2 , b is 1, and B forms the rest of an aryl or a C 3-7 heterocyclic group fused to the phenyl ring; excluding 1-[2-[2-(phenylmethyl)phenoxy]ethyl]-4-[(2,3,4-trimethoxyphenyl)methyl]-piperazine and pharmaceutically acceptable salts thereof, and nN-[4-[2-[4-[(3,4-dimethoxyphenyl)methyl]-1-piperazinyl]ethoxy]phenyl]-ethanesulfonamide and pharmaceutically acceptable salts thereof. Methods of preparing the compounds and uses of the compounds in therapy, in particular for CNS disorders such as depression and anxiety, are also disclosed.
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priorityDate 2002-02-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424705459
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID69764359
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID407655785
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128521020
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10126760
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11394642
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID69764360
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226397124
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID78124
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3696
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10195818
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421285479
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458392451
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424712012
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID455561966
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424712016
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128445969
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450198846
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID455561969
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11254267
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9229
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID65856
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424705523
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18987048
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5284566
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458396411
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9221
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Total number of triples: 1291.