http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0975593-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c2b9dc89cc4ba060cc73bbf0c90bbb78
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-08
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filingDate 1998-04-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eba079f32bcbec4cc344ea121dc53381
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_123b8ffcaf5460cda2002f105db51a95
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_123e73e40f33cd0f4b9dbb3faea3fa9d
publicationDate 2000-02-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0975593-A1
titleOfInvention Indole derivatives having combined 5ht1a, 5ht1b and 5ht1d receptor antagonist activity
abstract Compounds of formula (I), processes for their preparation and their use as CNS agents are disclosed, in which Ra is a group of formula (i), in which P1 is phenyl, bicyclic aryl, a 5- to 7-membered heterocyclic ring containing 1 to 3 heteroatoms selected from oxygen, nitrogen and sulphur, or a bicyclic heterocyclic ring containing 1 to 3 heteroatoms selected from oxygen, nitrogen and sulphur; R1 is hydrogen, halogen, C¿1-6?alkyl, C3-6cycloalkyl, COC1-6alkyl, C1-6alkoxy, hydroxy, hydroxyC1-6alkyl, hydroxyC1-6alkoxy, C1-6alkoxyC1-6alkoxy, C1-6alkanoyl, nitro, trifluoromethyl, cyano, SR?9, SOR9, SO¿2R9, SO2NR?1OR11, CO¿2R?10, CONR10R11, CO¿2NR?10R11, CONR10(CH¿2)cCO2R11, (CH2)cNR?10R11, (CH¿2)cCONR?10R11, (CH¿2)cNR?10COR11, (CH¿2)cCO2C1-6alkyl, CO2(CH2)cOR?10, NR10R11, NR10CO¿2R?11, NR10CONR10R11, CR10=NOR11, NR10COOR11, CNR10=NOR11¿, where R?10 and R11¿ are independently hydrogen or C¿1-6?alkyl and c is 1 to 4; R?2¿ is hydrogen, halogen, C¿1-6?alkyl, C3-6cycloalkyl, C3-6cycloalkenyl, C1-6alkoxy, acyl, aryl, acyloxy, hydroxy, nitro, trifluoromethyl, cyano, CO2R?10, CONR10R11, NR10R11¿ where R?10 and R11¿ are as defined for R1; a is 1, 2 or 3; or Ra is a group of formula (ii), wherein P?2 and P3¿ are independently phenyl, bicyclic aryl, a 5- to 7-membered heterocyclic ring containing 1 to 3 heteroatoms selected from oxygen, nitrogen and sulphur, or a bicyclic heterocyclic group containing 1 to 3 heteroatoms selected from oxygen, nitrogen or sulphur; A is a bond or oxygen, S(O)¿m? where m is 0 to 2, carbonyl, CH2 or NR?4¿ where R4 is hydrogen or C¿1-6?alkyl; R?1¿ is as defined above for formula (I) or R1 is an optionally substituted 5 to 7-membered heterocyclic ring containing 1 to 3 heteroatoms selected from oxygen, nitrogen or sulphur; R?2 and R3¿ are independently hydrogen, halogen, C¿1-6?alkyl, C3-6cycloalkyl, C3-6cycloalkenyl, C1-6alkoxy, acyl, aryl, acyloxy, hydroxy, nitro, trifluoromethyl, cyano, CO2R?10, CONR10R11, NR10R11¿ where R?10 and R11¿ are as defined for R1; and a and b are independently 1, 2 or 3; Y is -NH-, NR5 where R5 is C¿1-6?alkyl, or Y is -CH2- or -O-; V is oxygen or sulphur; D is nitrogen, carbon or a CH group; W is (CR?16R17)¿t where t is 2, 3 or 4 and R?16 and R17¿ are independently hydrogen or C¿1-6?alkyl or W is (CR?16R17)¿u-J where u is 0, 1, 2 or 3 and J is oxygen, sulphur, CR?16=CR17, CR16=N, =CR16O, =CR16¿S or =CR16-NR17; X is nitrogen or carbon; Rb is hydrogen, halogen, hydroxy, C¿1-6?alkyl, trifluoromethyl, C1-6alkoxy, C2-6alkenyl, C3-7cycloalkyl optionally substituted by C1-4alkyl, or aryl; R?c¿ is hydrogen or C¿1-6?alkyl; and ..... is a single bond when X is nitrogen or a single or double bond when X is carbon.
priorityDate 1997-04-18-04:00^^<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/compound/CID57297483
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID40467203
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226429576
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226769562
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226421593
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID78345
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID54079732
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID78344
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID53791464
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129050500
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422318393
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420754760
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457311044
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424366983
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID70284843
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24613
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226802102
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID53696545
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127942279
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129348053
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID338536
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129701402
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7221
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129605523
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID57181175
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226554904
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424922476
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID53884379
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127968426
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID53749240
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22462548
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID402
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226548335
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID233660963
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID57188345
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415775035
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID57165506
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20507215
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID227238505
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID54334117
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID228192159
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID229014421

Total number of triples: 1564.