CA2142721A1 - Condensed indole derivatives as 5ht and 5ht antagonists - Google Patents
Condensed indole derivatives as 5ht and 5ht antagonistsInfo
- Publication number
- CA2142721A1 CA2142721A1 CA002142721A CA2142721A CA2142721A1 CA 2142721 A1 CA2142721 A1 CA 2142721A1 CA 002142721 A CA002142721 A CA 002142721A CA 2142721 A CA2142721 A CA 2142721A CA 2142721 A1 CA2142721 A1 CA 2142721A1
- Authority
- CA
- Canada
- Prior art keywords
- methyl
- indole
- dihydropyrrolo
- pyridylcarbamoyl
- hydrogen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 150000002475 indoles Chemical class 0.000 title description 5
- 229940054051 antipsychotic indole derivative Drugs 0.000 title 1
- 239000003420 antiserotonin agent Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 135
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 53
- 239000001257 hydrogen Substances 0.000 claims abstract description 46
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 26
- 150000003839 salts Chemical class 0.000 claims abstract description 18
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims abstract description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 16
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 13
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 12
- 150000002367 halogens Chemical group 0.000 claims abstract description 12
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 10
- 150000002431 hydrogen Chemical group 0.000 claims abstract description 7
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 4
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000005864 Sulphur Chemical group 0.000 claims abstract description 3
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims abstract description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000001301 oxygen Chemical group 0.000 claims abstract description 3
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 3
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims abstract 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims abstract 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims description 146
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 claims description 64
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 claims description 64
- 238000000034 method Methods 0.000 claims description 37
- -1 1-(3-Pyridylcarbamoyl)-2,3-dihydropyrrolo[2,3-f]indole 6-Methyl-3-(4-pyridylcarbamoyl)-2,3-dihydropyrrolo[3,2-e]indole 6-Methyl-3-(2-pyridylcarbamoyl)-2,3-dihydropyrrolo[3,2-e]indole Chemical compound 0.000 claims description 20
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 15
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 9
- 238000002360 preparation method Methods 0.000 claims description 7
- CQILOHWHIWNQOE-UHFFFAOYSA-N indole-1-carboxamide Chemical compound C1=CC=C2N(C(=O)N)C=CC2=C1 CQILOHWHIWNQOE-UHFFFAOYSA-N 0.000 claims description 5
- 230000008569 process Effects 0.000 claims description 5
- 238000005859 coupling reaction Methods 0.000 claims description 4
- 239000008194 pharmaceutical composition Substances 0.000 claims description 4
- 230000008878 coupling Effects 0.000 claims description 3
- 238000010168 coupling process Methods 0.000 claims description 3
- 125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 claims description 3
- 125000000524 functional group Chemical group 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 238000002560 therapeutic procedure Methods 0.000 claims description 2
- YBGNQEMICNYGIU-UHFFFAOYSA-N 1,3-dimethyl-n-pyridin-3-yl-7,8-dihydropyrrolo[3,2-e]indole-6-carboxamide Chemical compound C1CC2=C3C(C)=CN(C)C3=CC=C2N1C(=O)NC1=CC=CN=C1 YBGNQEMICNYGIU-UHFFFAOYSA-N 0.000 claims 1
- QAAZWNMOAPVHLY-UHFFFAOYSA-N 1-methyl-n-(3-methyl-1,2-thiazol-5-yl)-6,7-dihydropyrrolo[2,3-f]indole-5-carboxamide Chemical compound S1N=C(C)C=C1NC(=O)N1C2=CC(C=CN3C)=C3C=C2CC1 QAAZWNMOAPVHLY-UHFFFAOYSA-N 0.000 claims 1
- YQYADMDNTTVUIL-UHFFFAOYSA-N 1-methyl-n-pyrazin-2-yl-6,7-dihydropyrrolo[2,3-f]indole-5-carboxamide Chemical compound C1CC=2C=C3N(C)C=CC3=CC=2N1C(=O)NC1=CN=CC=N1 YQYADMDNTTVUIL-UHFFFAOYSA-N 0.000 claims 1
- GMSRWMJQHSAGRF-UHFFFAOYSA-N 1-methyl-n-quinolin-5-yl-6,7-dihydropyrrolo[2,3-f]indole-5-carboxamide Chemical compound C1=CC=C2C(NC(=O)N3C=4C=C5C=CN(C5=CC=4CC3)C)=CC=CC2=N1 GMSRWMJQHSAGRF-UHFFFAOYSA-N 0.000 claims 1
- JZHFIMHXTLPLRX-UHFFFAOYSA-N 3-methyl-N-(2-methylquinolin-4-yl)-7,8-dihydropyrrolo[3,2-e]indole-6-carboxamide 3-methyl-N-pyridin-3-yl-8,9-dihydro-7H-pyrrolo[3,2-f]quinoline-6-carboxamide Chemical compound CN1C=CC2=C3C(=CC=C12)N(CC3)C(NC3=CC(=NC1=CC=CC=C31)C)=O.CN3C=CC1=C2CCCN(C2=CC=C13)C(=O)NC=1C=NC=CC1 JZHFIMHXTLPLRX-UHFFFAOYSA-N 0.000 claims 1
- ADOFDMVNOOWTIA-UHFFFAOYSA-N 3-methyl-N-pyridin-3-yl-7,8-dihydropyrrolo[3,2-e]indole-6-carboxamide 1-methyl-N-pyridin-3-yl-6,7-dihydropyrrolo[2,3-f]indole-5-carboxamide Chemical compound CN1C=CC2=C3C(=CC=C12)N(CC3)C(NC=3C=NC=CC3)=O.CN3C=CC=1C=C2C(=CC31)CCN2C(NC=2C=NC=CC2)=O ADOFDMVNOOWTIA-UHFFFAOYSA-N 0.000 claims 1
- OISBKHDJEYRHLR-UHFFFAOYSA-N 3-methyl-n-quinolin-5-yl-7,8-dihydropyrrolo[3,2-e]indole-6-carboxamide Chemical compound C1=CC=C2C(NC(=O)N3CCC4=C5C=CN(C5=CC=C43)C)=CC=CC2=N1 OISBKHDJEYRHLR-UHFFFAOYSA-N 0.000 claims 1
- YVXBHIFSSHPBDE-UHFFFAOYSA-N 6-methyl-n-pyridin-3-yl-1,2,7,8-tetrahydropyrrolo[3,2-e]indole-3-carboxamide Chemical compound C12=CC=C3N(C)CCC3=C2CCN1C(=O)NC1=CC=CN=C1 YVXBHIFSSHPBDE-UHFFFAOYSA-N 0.000 claims 1
- 101100243950 Arabidopsis thaliana PIE1 gene Proteins 0.000 claims 1
- IDWSQLGXCSPWJH-UHFFFAOYSA-N CN1C(=CC=2C=C3C(=CC12)CCN3C(NC=3C=NC=CC3)=O)C.C(CC)N3C=CC=1C=C2C(=CC31)CCN2C(NC=2C=NC=CC2)=O Chemical compound CN1C(=CC=2C=C3C(=CC12)CCN3C(NC=3C=NC=CC3)=O)C.C(CC)N3C=CC=1C=C2C(=CC31)CCN2C(NC=2C=NC=CC2)=O IDWSQLGXCSPWJH-UHFFFAOYSA-N 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 abstract description 14
- 238000011282 treatment Methods 0.000 abstract description 9
- 229940044551 receptor antagonist Drugs 0.000 abstract description 6
- 239000002464 receptor antagonist Substances 0.000 abstract description 6
- 102000006969 5-HT2B Serotonin Receptor Human genes 0.000 abstract description 3
- 108010072584 5-HT2B Serotonin Receptor Proteins 0.000 abstract description 3
- 102000006902 5-HT2C Serotonin Receptor Human genes 0.000 abstract description 3
- 108010072553 5-HT2C Serotonin Receptor Proteins 0.000 abstract description 3
- 208000019901 Anxiety disease Diseases 0.000 abstract description 3
- 230000036506 anxiety Effects 0.000 abstract description 3
- 208000015114 central nervous system disease Diseases 0.000 abstract 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 59
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 57
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 54
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 49
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 46
- 229910001868 water Inorganic materials 0.000 description 43
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 39
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N DMSO Substances CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 38
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 37
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 37
- 239000007787 solid Substances 0.000 description 37
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 31
- 239000000203 mixture Substances 0.000 description 31
- 101150041968 CDC13 gene Proteins 0.000 description 29
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 28
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 24
- 239000000243 solution Substances 0.000 description 24
- 239000003921 oil Substances 0.000 description 18
- 235000019198 oils Nutrition 0.000 description 18
- 239000000741 silica gel Substances 0.000 description 18
- 229910002027 silica gel Inorganic materials 0.000 description 18
- 235000019439 ethyl acetate Nutrition 0.000 description 17
- 150000002500 ions Chemical class 0.000 description 16
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 15
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- 229940093499 ethyl acetate Drugs 0.000 description 15
- 239000011734 sodium Substances 0.000 description 14
- 239000002253 acid Substances 0.000 description 13
- 238000004587 chromatography analysis Methods 0.000 description 13
- 239000000725 suspension Substances 0.000 description 13
- 241000700159 Rattus Species 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- 238000010992 reflux Methods 0.000 description 11
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 10
- 125000001041 indolyl group Chemical group 0.000 description 10
- 229910052708 sodium Inorganic materials 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 9
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 9
- 208000035475 disorder Diseases 0.000 description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 125000000217 alkyl group Chemical group 0.000 description 8
- PFKFTWBEEFSNDU-UHFFFAOYSA-N carbonyldiimidazole Chemical compound C1=CN=CN1C(=O)N1C=CN=C1 PFKFTWBEEFSNDU-UHFFFAOYSA-N 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 238000004440 column chromatography Methods 0.000 description 7
- 239000003814 drug Substances 0.000 description 7
- 238000001035 drying Methods 0.000 description 7
- 229910000027 potassium carbonate Inorganic materials 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- 239000000377 silicon dioxide Substances 0.000 description 7
- 229910052717 sulfur Inorganic materials 0.000 description 7
- 239000003981 vehicle Substances 0.000 description 7
- VHFVKMTVMIZMIK-UHFFFAOYSA-N 1-(3-chlorophenyl)piperazine Chemical compound ClC1=CC=CC(N2CCNCC2)=C1 VHFVKMTVMIZMIK-UHFFFAOYSA-N 0.000 description 6
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- 241000400611 Eucalyptus deanei Species 0.000 description 6
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 6
- 150000001408 amides Chemical class 0.000 description 6
- 229910052681 coesite Inorganic materials 0.000 description 6
- 229910052906 cristobalite Inorganic materials 0.000 description 6
- 229940079593 drug Drugs 0.000 description 6
- 238000001914 filtration Methods 0.000 description 6
- 239000012442 inert solvent Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
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- 235000012239 silicon dioxide Nutrition 0.000 description 6
- 229910052682 stishovite Inorganic materials 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
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- AFVFQIVMOAPDHO-UHFFFAOYSA-M Methanesulfonate Chemical compound CS([O-])(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-M 0.000 description 5
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- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 5
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 5
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- 239000002904 solvent Substances 0.000 description 5
- WWORPZXUCHHSOT-UHFFFAOYSA-N 3-methyl-n-pyridin-3-yl-7,8-dihydropyrrolo[3,2-e]indole-6-carboxamide Chemical compound C12=CC=C3N(C)C=CC3=C2CCN1C(=O)NC1=CC=CN=C1 WWORPZXUCHHSOT-UHFFFAOYSA-N 0.000 description 4
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- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- XMIAFAKRAAMSGX-UHFFFAOYSA-N quinolin-5-amine Chemical compound C1=CC=C2C(N)=CC=CC2=N1 XMIAFAKRAAMSGX-UHFFFAOYSA-N 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- JUQLTPCYUFPYKE-UHFFFAOYSA-N ritanserin Chemical compound CC=1N=C2SC=CN2C(=O)C=1CCN(CC1)CCC1=C(C=1C=CC(F)=CC=1)C1=CC=C(F)C=C1 JUQLTPCYUFPYKE-UHFFFAOYSA-N 0.000 description 1
- 229950009626 ritanserin Drugs 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000000932 sedative agent Substances 0.000 description 1
- 230000001624 sedative effect Effects 0.000 description 1
- 239000002891 serotonin 2B antagonist Substances 0.000 description 1
- 239000002484 serotonin 2C antagonist Substances 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 208000019116 sleep disease Diseases 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000004149 tartrazine Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000759 toxicological effect Toxicity 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
- 125000004044 trifluoroacetyl group Chemical group FC(C(=O)*)(F)F 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
- Indole Compounds (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9217674.2 | 1992-08-20 | ||
| GB929217674A GB9217674D0 (en) | 1992-08-20 | 1992-08-20 | Novel compounds |
| GB9306461.6 | 1993-03-29 | ||
| GB939306461A GB9306461D0 (en) | 1993-03-29 | 1993-03-29 | Novel compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2142721A1 true CA2142721A1 (en) | 1994-03-03 |
Family
ID=26301461
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002142721A Abandoned CA2142721A1 (en) | 1992-08-20 | 1993-07-29 | Condensed indole derivatives as 5ht and 5ht antagonists |
Country Status (13)
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9306460D0 (en) * | 1993-03-29 | 1993-05-19 | Smithkline Beecham Plc | Novel compounds |
| GB9313913D0 (en) * | 1993-07-06 | 1993-08-18 | Smithkline Beecham Plc | Novel compounds |
| GB9402542D0 (en) * | 1994-02-10 | 1994-04-06 | Smith Kline Beecham Plc | Novel compounds |
| EP0757687A1 (en) * | 1994-04-23 | 1997-02-12 | Smithkline Beecham Plc | Tricyclic derivatives as 5ht 2c? and 5ht 2b? antagonists |
| GB9420521D0 (en) * | 1994-10-12 | 1994-11-30 | Smithkline Beecham Plc | Novel compounds |
| GB9420999D0 (en) * | 1994-10-18 | 1994-12-07 | Smithkline Beecham Plc | Novel compounds |
| US5972937A (en) * | 1995-02-02 | 1999-10-26 | Smithkline Beecham P.L.C. | Heterocyclic compounds possessing 5HT2C receptor antagonist activity |
| KR19980701879A (ko) * | 1995-02-02 | 1998-06-25 | 피터 기딩스 | 5-히드록시트립타민 수용체 길항제로서의 인돌 유도체 |
| GB9517559D0 (en) * | 1995-08-26 | 1995-10-25 | Smithkline Beecham Plc | Novel compounds |
| GB9607219D0 (en) * | 1996-04-04 | 1996-06-12 | Smithkline Beecham Plc | Novel compounds |
| GB9612885D0 (en) * | 1996-06-20 | 1996-08-21 | Smithkline Beecham Plc | Novel compounds |
| GB9612883D0 (en) | 1996-06-20 | 1996-08-21 | Smithkline Beecham Plc | Novel compounds |
| JP2001508767A (ja) * | 1996-12-02 | 2001-07-03 | 藤沢薬品工業株式会社 | ５―ｈｔ拮抗作用を有するインドール―ウレア誘導体 |
| GB9724372D0 (en) * | 1997-11-18 | 1998-01-14 | Smithkline Beecham Plc | Novel compounds |
| UA77650C2 (en) | 1999-12-06 | 2007-01-15 | Lundbeck & Co As H | Use of serotonin reuptake inhibitor in combination with deramcyclane |
| FR2807754A1 (fr) * | 2000-04-13 | 2001-10-19 | Adir | Nouveaux derives de cyclobuta-indole carboxamide, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| FR2837823B1 (fr) * | 2002-03-27 | 2005-04-08 | Servier Lab | Nouveaux derives d'indoline, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| WO2004057338A1 (en) * | 2002-12-23 | 2004-07-08 | Bayer Healthcare Ag | Diagnostics and therapeutics for diseases assosciated with 5-hydroxytryptamine (serotonin) receptor 2b (5-hteb) |
| GB0305553D0 (en) * | 2003-03-11 | 2003-04-16 | Glaxo Group Ltd | Compounds |
| WO2014049153A1 (en) * | 2012-09-28 | 2014-04-03 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Antagonists of the 5-ht2b receptor for use in the prevention or treatment of spasticity |
| EP4175637A4 (en) * | 2020-07-02 | 2024-08-07 | Purdue Research Foundation | Tetrahydro-3h-pyrazolo quinolone and tetrahydro-3h-pyrrolo[3,2-f]quinoline-containing compounds and uses thereof |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU642041B2 (en) * | 1990-09-13 | 1993-10-07 | Beecham Group Plc | Indole ureas as 5 HT receptor antagonist |
-
1993
- 1993-07-29 JP JP6505828A patent/JPH08500580A/ja active Pending
- 1993-07-29 WO PCT/EP1993/002031 patent/WO1994004533A1/en not_active Application Discontinuation
- 1993-07-29 EP EP93917699A patent/EP0656003A1/en not_active Ceased
- 1993-07-29 NZ NZ254785A patent/NZ254785A/en unknown
- 1993-07-29 CA CA002142721A patent/CA2142721A1/en not_active Abandoned
- 1993-07-29 AU AU47046/93A patent/AU4704693A/en not_active Abandoned
- 1993-08-18 MX MX9305037A patent/MX9305037A/es unknown
- 1993-08-18 MA MA23262A patent/MA22955A1/fr unknown
- 1993-08-19 AP APAP/P/1993/000560A patent/AP9300560A0/en unknown
- 1993-08-19 CN CN93116553A patent/CN1086819A/zh active Pending
- 1993-08-19 IL IL10673793A patent/IL106737A0/xx unknown
- 1993-08-19 TW TW082106679A patent/TW248557B/zh active
- 1993-08-20 SI SI9300438A patent/SI9300438A/sl unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AP9300560A0 (en) | 1995-02-19 |
| NZ254785A (en) | 1995-09-26 |
| MA22955A1 (fr) | 1994-04-01 |
| CN1086819A (zh) | 1994-05-18 |
| SI9300438A (en) | 1994-03-31 |
| JPH08500580A (ja) | 1996-01-23 |
| EP0656003A1 (en) | 1995-06-07 |
| AU4704693A (en) | 1994-03-15 |
| MX9305037A (es) | 1994-03-31 |
| TW248557B (enrdf_load_stackoverflow) | 1995-06-01 |
| IL106737A0 (en) | 1994-05-30 |
| WO1994004533A1 (en) | 1994-03-03 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |