NO317257B1 - Indolderivater og farmasoytiske sammensetninger omfattende det samme - Google Patents
Indolderivater og farmasoytiske sammensetninger omfattende det samme Download PDFInfo
- Publication number
- NO317257B1 NO317257B1 NO20004277A NO20004277A NO317257B1 NO 317257 B1 NO317257 B1 NO 317257B1 NO 20004277 A NO20004277 A NO 20004277A NO 20004277 A NO20004277 A NO 20004277A NO 317257 B1 NO317257 B1 NO 317257B1
- Authority
- NO
- Norway
- Prior art keywords
- ethyl
- propyl
- compound
- solution
- amino
- Prior art date
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- 150000002475 indoles Chemical class 0.000 title claims description 21
- 239000008194 pharmaceutical composition Substances 0.000 title claims description 9
- 229940054051 antipsychotic indole derivative Drugs 0.000 title description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 25
- 125000004432 carbon atom Chemical group C* 0.000 claims description 25
- -1 pivaloyloxy group Chemical group 0.000 claims description 24
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 22
- 150000003839 salts Chemical class 0.000 claims description 21
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims description 13
- 208000010412 Glaucoma Diseases 0.000 claims description 9
- 230000004410 intraocular pressure Effects 0.000 claims description 9
- 206010030043 Ocular hypertension Diseases 0.000 claims description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
- 238000002360 preparation method Methods 0.000 claims description 8
- 230000002265 prevention Effects 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 6
- 239000004480 active ingredient Substances 0.000 claims description 4
- 239000000470 constituent Substances 0.000 claims description 2
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 102
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 81
- 239000000243 solution Substances 0.000 description 54
- 150000001875 compounds Chemical class 0.000 description 49
- 239000000203 mixture Substances 0.000 description 36
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 28
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 21
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 21
- 229940126062 Compound A Drugs 0.000 description 19
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 19
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 19
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 17
- 239000002904 solvent Substances 0.000 description 17
- 238000012360 testing method Methods 0.000 description 16
- 238000005160 1H NMR spectroscopy Methods 0.000 description 15
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
- 230000000694 effects Effects 0.000 description 14
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical class CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 14
- 235000017557 sodium bicarbonate Nutrition 0.000 description 14
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 14
- 239000012267 brine Substances 0.000 description 13
- 239000012530 fluid Substances 0.000 description 13
- 239000011541 reaction mixture Substances 0.000 description 13
- 229920006395 saturated elastomer Polymers 0.000 description 13
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 13
- 239000003889 eye drop Substances 0.000 description 12
- 229940012356 eye drops Drugs 0.000 description 12
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 12
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 11
- 239000003795 chemical substances by application Substances 0.000 description 11
- 238000001816 cooling Methods 0.000 description 10
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 8
- 239000013078 crystal Substances 0.000 description 8
- 238000004440 column chromatography Methods 0.000 description 7
- 229940079593 drug Drugs 0.000 description 7
- 239000003814 drug Substances 0.000 description 7
- 239000003480 eluent Substances 0.000 description 7
- 239000000741 silica gel Substances 0.000 description 7
- 229910002027 silica gel Inorganic materials 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- VZTDIZULWFCMLS-UHFFFAOYSA-N ammonium formate Chemical compound [NH4+].[O-]C=O VZTDIZULWFCMLS-UHFFFAOYSA-N 0.000 description 6
- 230000035699 permeability Effects 0.000 description 6
- 230000003389 potentiating effect Effects 0.000 description 6
- 238000010992 reflux Methods 0.000 description 6
- 101150041968 CDC13 gene Proteins 0.000 description 5
- 239000008280 blood Substances 0.000 description 5
- 210000004369 blood Anatomy 0.000 description 5
- 230000037396 body weight Effects 0.000 description 5
- 230000008602 contraction Effects 0.000 description 5
- 239000012153 distilled water Substances 0.000 description 5
- 238000004128 high performance liquid chromatography Methods 0.000 description 5
- 239000012528 membrane Substances 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 230000035515 penetration Effects 0.000 description 5
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 5
- LPAJCOGMIXSKKG-GOSISDBHSA-N 5-[(2r)-2-[2-(2-ethoxyphenoxy)ethylamino]propyl]-1-(3-hydroxypropyl)indole-7-carboxamide Chemical compound CCOC1=CC=CC=C1OCCN[C@H](C)CC1=CC(C(N)=O)=C(N(CCCO)C=C2)C2=C1 LPAJCOGMIXSKKG-GOSISDBHSA-N 0.000 description 4
- 208000001953 Hypotension Diseases 0.000 description 4
- 208000001089 Multiple system atrophy Diseases 0.000 description 4
- 238000005481 NMR spectroscopy Methods 0.000 description 4
- 206010031127 Orthostatic hypotension Diseases 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- IUGQFMIATSVYLK-UHFFFAOYSA-N benzyl 2-(4-hydroxyphenyl)acetate Chemical compound C1=CC(O)=CC=C1CC(=O)OCC1=CC=CC=C1 IUGQFMIATSVYLK-UHFFFAOYSA-N 0.000 description 4
- 229960003612 bunazosin hydrochloride Drugs 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 230000036543 hypotension Effects 0.000 description 4
- QMKUYPGVVVLYSR-UHFFFAOYSA-N propyl 2,2-dimethylpropanoate Chemical compound CCCOC(=O)C(C)(C)C QMKUYPGVVVLYSR-UHFFFAOYSA-N 0.000 description 4
- 125000006239 protecting group Chemical group 0.000 description 4
- DYHSDKLCOJIUFX-UHFFFAOYSA-N tert-butoxycarbonyl anhydride Chemical compound CC(C)(C)OC(=O)OC(=O)OC(C)(C)C DYHSDKLCOJIUFX-UHFFFAOYSA-N 0.000 description 4
- UUQSFEQUZOKCHP-OAQYLSRUSA-N tert-butyl n-[(2r)-1-[7-carbamoyl-1-(3-hydroxypropyl)-2,3-dihydroindol-5-yl]propan-2-yl]-n-[2-(2-ethoxyphenoxy)ethyl]carbamate Chemical compound CCOC1=CC=CC=C1OCCN(C(=O)OC(C)(C)C)[C@H](C)CC(C=C1C(N)=O)=CC2=C1N(CCCO)CC2 UUQSFEQUZOKCHP-OAQYLSRUSA-N 0.000 description 4
- SFLSHLFXELFNJZ-QMMMGPOBSA-N (-)-norepinephrine Chemical compound NC[C@H](O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-QMMMGPOBSA-N 0.000 description 3
- CTMYLDUPTAZFCT-OAQYLSRUSA-N 3-[7-carbamoyl-5-[(2r)-2-[2-(2-ethoxyphenoxy)ethylamino]propyl]indol-1-yl]propyl 2,2-dimethylpropanoate Chemical compound CCOC1=CC=CC=C1OCCN[C@H](C)CC1=CC(C(N)=O)=C(N(CCCOC(=O)C(C)(C)C)C=C2)C2=C1 CTMYLDUPTAZFCT-OAQYLSRUSA-N 0.000 description 3
- OKXAFOMCBQVAHI-ZMBIFBSDSA-N 3-[7-carbamoyl-5-[(2r)-2-[2-(2-ethoxyphenoxy)ethylamino]propyl]indol-1-yl]propyl 2,2-dimethylpropanoate;hydrochloride Chemical compound Cl.CCOC1=CC=CC=C1OCCN[C@H](C)CC1=CC(C(N)=O)=C(N(CCCOC(=O)C(C)(C)C)C=C2)C2=C1 OKXAFOMCBQVAHI-ZMBIFBSDSA-N 0.000 description 3
- ZYBXLNNJVLQAIN-GOSISDBHSA-N 5-[(2r)-2-[2-(2-ethoxyphenoxy)ethylamino]propyl]-1-(3-hydroxypropyl)-2,3-dihydroindole-7-carboxamide Chemical compound CCOC1=CC=CC=C1OCCN[C@H](C)CC(C=C1C(N)=O)=CC2=C1N(CCCO)CC2 ZYBXLNNJVLQAIN-GOSISDBHSA-N 0.000 description 3
- GPWOZMLUYFBWBB-GMUIIQOCSA-N 5-[(2r)-2-[2-(2-ethoxyphenoxy)ethylamino]propyl]-1-(3-hydroxypropyl)indole-7-carboxamide;hydrochloride Chemical compound Cl.CCOC1=CC=CC=C1OCCN[C@H](C)CC1=CC(C(N)=O)=C(N(CCCO)C=C2)C2=C1 GPWOZMLUYFBWBB-GMUIIQOCSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 3
- 108090000604 Hydrolases Proteins 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 241000700159 Rattus Species 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000000903 blocking effect Effects 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 235000015165 citric acid Nutrition 0.000 description 3
- 210000004087 cornea Anatomy 0.000 description 3
- 230000005284 excitation Effects 0.000 description 3
- 238000005558 fluorometry Methods 0.000 description 3
- 150000002476 indolines Chemical class 0.000 description 3
- 238000009434 installation Methods 0.000 description 3
- 229960002748 norepinephrine Drugs 0.000 description 3
- SFLSHLFXELFNJZ-UHFFFAOYSA-N norepinephrine Natural products NCC(O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-UHFFFAOYSA-N 0.000 description 3
- 239000008363 phosphate buffer Substances 0.000 description 3
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- VICSLOHTZDWOFF-QGZVFWFLSA-N 1-(3-hydroxypropyl)-5-[(2r)-2-[2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethylamino]propyl]indole-7-carboxamide Chemical compound N([C@@H](CC=1C=C2C=CN(CCCO)C2=C(C(N)=O)C=1)C)CCOC1=CC=CC=C1OCC(F)(F)F VICSLOHTZDWOFF-QGZVFWFLSA-N 0.000 description 2
- OXQGTIUCKGYOAA-UHFFFAOYSA-N 2-Ethylbutanoic acid Chemical class CCC(CC)C(O)=O OXQGTIUCKGYOAA-UHFFFAOYSA-N 0.000 description 2
- SMUKODJVMQOSAB-UHFFFAOYSA-N 2-ethylbutanoyl chloride Chemical compound CCC(CC)C(Cl)=O SMUKODJVMQOSAB-UHFFFAOYSA-N 0.000 description 2
- SPIYQPPDQNLNDT-MRXNPFEDSA-N 3-[5-[(2r)-2-aminopropyl]-7-cyano-2,3-dihydroindol-1-yl]propyl benzoate Chemical compound C1=2C(C#N)=CC(C[C@H](N)C)=CC=2CCN1CCCOC(=O)C1=CC=CC=C1 SPIYQPPDQNLNDT-MRXNPFEDSA-N 0.000 description 2
- CBFCMNHKMMHMPJ-XMMPIXPASA-N 3-[7-carbamoyl-5-[(2r)-2-[(2-methylpropan-2-yl)oxycarbonyl-[2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethyl]amino]propyl]indol-1-yl]propyl 2-ethylbutanoate Chemical compound CC(C)(C)OC(=O)N([C@H](C)CC=1C=C2C=CN(C2=C(C(N)=O)C=1)CCCOC(=O)C(CC)CC)CCOC1=CC=CC=C1OCC(F)(F)F CBFCMNHKMMHMPJ-XMMPIXPASA-N 0.000 description 2
- BSMVRQLNZFJKRJ-XMMPIXPASA-N 3-[7-carbamoyl-5-[(2r)-2-[2-(2-ethoxyphenoxy)ethyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]propyl]-2,3-dihydroindol-1-yl]propyl 2,2-dimethylpropanoate Chemical compound CCOC1=CC=CC=C1OCCN(C(=O)OC(C)(C)C)[C@H](C)CC(C=C1C(N)=O)=CC2=C1N(CCCOC(=O)C(C)(C)C)CC2 BSMVRQLNZFJKRJ-XMMPIXPASA-N 0.000 description 2
- IENUJLYMYCPJBQ-XMMPIXPASA-N 3-[7-cyano-5-[(2r)-2-[2-(2-ethoxyphenoxy)ethylamino]propyl]-2,3-dihydroindol-1-yl]propyl benzoate Chemical compound CCOC1=CC=CC=C1OCCN[C@H](C)CC(C=C1C#N)=CC2=C1N(CCCOC(=O)C=1C=CC=CC=1)CC2 IENUJLYMYCPJBQ-XMMPIXPASA-N 0.000 description 2
- DBQYWUDHQGTRCW-LJQANCHMSA-N 5-[(2r)-2-[2-(2-ethoxyphenoxy)ethylamino]propyl]-1-(3-hydroxypropyl)-2,3-dihydroindole-7-carbonitrile Chemical compound CCOC1=CC=CC=C1OCCN[C@H](C)CC(C=C1C#N)=CC2=C1N(CCCO)CC2 DBQYWUDHQGTRCW-LJQANCHMSA-N 0.000 description 2
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- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
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- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 230000001603 reducing effect Effects 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
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- 238000010438 heat treatment Methods 0.000 description 1
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- 238000006460 hydrolysis reaction Methods 0.000 description 1
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- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- XXUPXHKCPIKWLR-JHUOEJJVSA-N isopropyl unoprostone Chemical compound CCCCCCCC(=O)CC[C@H]1[C@H](O)C[C@H](O)[C@@H]1C\C=C/CCCC(=O)OC(C)C XXUPXHKCPIKWLR-JHUOEJJVSA-N 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- FBBDOOHMGLLEGJ-UHFFFAOYSA-N methane;hydrochloride Chemical compound C.Cl FBBDOOHMGLLEGJ-UHFFFAOYSA-N 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- OLXYLDUSSBULGU-UHFFFAOYSA-N methyl pyridine-4-carboxylate Chemical compound COC(=O)C1=CC=NC=C1 OLXYLDUSSBULGU-UHFFFAOYSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- DZAQGDJIAAXOAG-UHFFFAOYSA-N propyl 2,2-dimethylbutanoate Chemical compound CCCOC(=O)C(C)(C)CC DZAQGDJIAAXOAG-UHFFFAOYSA-N 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- PNCPYILNMDWPEY-QGZVFWFLSA-N silodosin Chemical compound N([C@@H](CC=1C=C(C=2N(CCCO)CCC=2C=1)C(N)=O)C)CCOC1=CC=CC=C1OCC(F)(F)F PNCPYILNMDWPEY-QGZVFWFLSA-N 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011775 sodium fluoride Substances 0.000 description 1
- 235000013024 sodium fluoride Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- ZYCYVMNPICJOBM-HXUWFJFHSA-N tert-butyl n-[(2r)-1-[7-carbamoyl-1-(3-hydroxypropyl)indol-5-yl]propan-2-yl]-n-[2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethyl]carbamate Chemical compound CC(C)(C)OC(=O)N([C@@H](CC=1C=C2C=CN(CCCO)C2=C(C(N)=O)C=1)C)CCOC1=CC=CC=C1OCC(F)(F)F ZYCYVMNPICJOBM-HXUWFJFHSA-N 0.000 description 1
- 210000001550 testis Anatomy 0.000 description 1
- 229960005221 timolol maleate Drugs 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 229950008081 unoprostone isopropyl Drugs 0.000 description 1
- 210000001177 vas deferen Anatomy 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- 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
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9057298 | 1998-02-27 | ||
| PCT/JP1999/000732 WO1999043652A1 (fr) | 1998-02-27 | 1999-02-19 | Derives de l'indole et compositions medicales les renfermant |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO20004277D0 NO20004277D0 (no) | 2000-08-25 |
| NO20004277L NO20004277L (no) | 2000-09-11 |
| NO317257B1 true NO317257B1 (no) | 2004-09-27 |
Family
ID=14002150
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20004277A NO317257B1 (no) | 1998-02-27 | 2000-08-25 | Indolderivater og farmasoytiske sammensetninger omfattende det samme |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US6310086B1 (da) |
| EP (1) | EP1057813B1 (da) |
| JP (1) | JP4342101B2 (da) |
| KR (1) | KR100576207B1 (da) |
| CN (1) | CN1157375C (da) |
| AR (1) | AR014964A1 (da) |
| AT (1) | ATE264841T1 (da) |
| AU (1) | AU766088B2 (da) |
| BR (1) | BR9908301A (da) |
| CA (1) | CA2321547C (da) |
| DE (1) | DE69916586T2 (da) |
| DK (1) | DK1057813T3 (da) |
| ES (1) | ES2220043T3 (da) |
| HK (1) | HK1036974A1 (da) |
| HU (1) | HUP0100680A3 (da) |
| NO (1) | NO317257B1 (da) |
| NZ (1) | NZ506497A (da) |
| PE (1) | PE20000329A1 (da) |
| PL (1) | PL342477A1 (da) |
| RU (1) | RU2212404C2 (da) |
| SK (1) | SK12722000A3 (da) |
| TW (2) | TWI249525B (da) |
| WO (1) | WO1999043652A1 (da) |
| ZA (1) | ZA991590B (da) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1157375C (zh) | 1998-02-27 | 2004-07-14 | 橘生药品工业株式会社 | 吲哚衍生物及其药物组合物 |
| JP4634560B2 (ja) * | 2000-01-14 | 2011-02-16 | キッセイ薬品工業株式会社 | 光学活性なインドリン誘導体の製造方法およびその製造中間体 |
| US6849655B2 (en) | 2000-05-15 | 2005-02-01 | Kissei Pharmaceutical Co., Ltd. | Aqueous liquid formulations |
| US7229986B2 (en) * | 2000-05-16 | 2007-06-12 | Takeda Pharmaceutical Company Ltd. | Melanin-concentrating hormone antagonist |
| JP4921646B2 (ja) * | 2001-03-08 | 2012-04-25 | キッセイ薬品工業株式会社 | １−（３−ベンジルオキシプロピル）−５−（２−置換プロピル）インドリン誘導体およびその使用方法 |
| CA2453476A1 (en) * | 2001-07-13 | 2003-01-23 | Kissei Pharmaceutical Co., Ltd. | Medicinal compositions for opthalmic use |
| HU225505B1 (en) * | 2002-09-09 | 2007-01-29 | Richter Gedeon Vegyeszet | Process for the preparation of r-(-)-tamsulosin hydrochloride and novel intermediates |
| AR050253A1 (es) | 2004-06-24 | 2006-10-11 | Smithkline Beecham Corp | Compuesto derivado de indazol carboxamida, composicion que lo comprende y su uso para la preparacion de un medicamento |
| ATE508113T1 (de) * | 2004-10-27 | 2011-05-15 | Kissei Pharmaceutical | Indolinverbindung und verfahren zu deren herstellung |
| WO2006137368A1 (ja) * | 2005-06-21 | 2006-12-28 | Kowa Co., Ltd. | 緑内障の予防又は治療剤 |
| US8063071B2 (en) | 2007-10-31 | 2011-11-22 | GlaxoSmithKline, LLC | Chemical compounds |
| US20100076010A1 (en) * | 2007-02-26 | 2010-03-25 | Concert Pharmaceuticals, Inc. | Alpha 1a-adrenoceptor antagonists |
| EP2125717B1 (en) * | 2007-02-26 | 2013-07-03 | Concert Pharmaceuticals Inc. | Deuterated derivatives of silodosin as alpha ia-adrenoreceptor antagonists |
| PE20081889A1 (es) | 2007-03-23 | 2009-03-05 | Smithkline Beecham Corp | Indol carboxamidas como inhibidores de ikk2 |
| WO2010102968A1 (en) | 2009-03-10 | 2010-09-16 | Glaxo Group Limited | Indole derivatives as ikk2 inhibitors |
| CN104211631A (zh) * | 2013-05-30 | 2014-12-17 | 中国科学院上海药物研究所 | 一类吲哚类化合物、其制备方法、药物组合物及应用 |
| WO2016042441A1 (en) | 2014-09-18 | 2016-03-24 | Mankind Research Centre | A novel process for the preparation of considerably pure silodosin |
| ES2607639B1 (es) | 2015-09-30 | 2018-02-28 | Urquima, S.A | Sal de ácido maleico de un intermedio de silodosina |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5021410A (en) | 1989-05-22 | 1991-06-04 | Allergan, Inc. | Combinations of selective alpha-adrenergic agonists and antagonists useful in lowering intraocular pressure |
| DE69319551T2 (de) | 1992-12-02 | 1998-10-29 | Kissei Pharmaceutical | Indolin Verbindungen zur Behandlung von Dysurien |
| JP3331048B2 (ja) * | 1994-06-01 | 2002-10-07 | キッセイ薬品工業株式会社 | インドール誘導体 |
| JP3331047B2 (ja) * | 1994-06-01 | 2002-10-07 | キッセイ薬品工業株式会社 | インドリン誘導体 |
| JPH08143557A (ja) * | 1994-11-24 | 1996-06-04 | Toyobo Co Ltd | 新規なフェニルピペラジン誘導体、その塩及びその溶媒和物 |
| JPH0912563A (ja) * | 1995-06-30 | 1997-01-14 | Toyobo Co Ltd | 新規ベンジルアルコ−ル誘導体、その製造方法およびその用途 |
| AU9095998A (en) * | 1997-09-22 | 1999-04-12 | Kissei Pharmaceutical Co. Ltd. | Remedies for dysuria resulting from prostatic hypertrophy |
| CN1157375C (zh) | 1998-02-27 | 2004-07-14 | 橘生药品工业株式会社 | 吲哚衍生物及其药物组合物 |
-
1999
- 1999-02-19 CN CNB998033219A patent/CN1157375C/zh not_active Expired - Lifetime
- 1999-02-19 AT AT99905242T patent/ATE264841T1/de not_active IP Right Cessation
- 1999-02-19 SK SK1272-2000A patent/SK12722000A3/sk unknown
- 1999-02-19 HU HU0100680A patent/HUP0100680A3/hu unknown
- 1999-02-19 PL PL99342477A patent/PL342477A1/xx not_active Application Discontinuation
- 1999-02-19 WO PCT/JP1999/000732 patent/WO1999043652A1/ja not_active Application Discontinuation
- 1999-02-19 DE DE69916586T patent/DE69916586T2/de not_active Expired - Lifetime
- 1999-02-19 RU RU2000122435/04A patent/RU2212404C2/ru not_active IP Right Cessation
- 1999-02-19 ES ES99905242T patent/ES2220043T3/es not_active Expired - Lifetime
- 1999-02-19 AU AU25478/99A patent/AU766088B2/en not_active Ceased
- 1999-02-19 EP EP99905242A patent/EP1057813B1/en not_active Expired - Lifetime
- 1999-02-19 KR KR1020007009536A patent/KR100576207B1/ko not_active IP Right Cessation
- 1999-02-19 DK DK99905242T patent/DK1057813T3/da active
- 1999-02-19 CA CA002321547A patent/CA2321547C/en not_active Expired - Fee Related
- 1999-02-19 BR BR9908301-9A patent/BR9908301A/pt not_active IP Right Cessation
- 1999-02-19 NZ NZ506497A patent/NZ506497A/xx unknown
- 1999-02-19 JP JP2000533410A patent/JP4342101B2/ja not_active Expired - Fee Related
- 1999-02-19 US US09/622,871 patent/US6310086B1/en not_active Expired - Lifetime
- 1999-02-22 TW TW088102531A patent/TWI249525B/zh active
- 1999-02-22 TW TW089116222A patent/TWI241293B/zh not_active IP Right Cessation
- 1999-02-26 ZA ZA9901590A patent/ZA991590B/xx unknown
- 1999-02-26 AR ARP990100809A patent/AR014964A1/es unknown
- 1999-02-26 PE PE1999000167A patent/PE20000329A1/es not_active Application Discontinuation
-
2000
- 2000-08-25 NO NO20004277A patent/NO317257B1/no unknown
-
2001
- 2001-09-24 HK HK01106719A patent/HK1036974A1/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| AR014964A1 (es) | 2001-04-11 |
| RU2212404C2 (ru) | 2003-09-20 |
| WO1999043652A1 (fr) | 1999-09-02 |
| TWI241293B (en) | 2005-10-11 |
| EP1057813A1 (en) | 2000-12-06 |
| KR100576207B1 (ko) | 2006-05-03 |
| NO20004277L (no) | 2000-09-11 |
| HK1036974A1 (en) | 2002-01-25 |
| KR20010041403A (ko) | 2001-05-15 |
| HUP0100680A2 (hu) | 2001-08-28 |
| CA2321547A1 (en) | 1999-09-02 |
| SK12722000A3 (sk) | 2001-03-12 |
| CA2321547C (en) | 2010-01-19 |
| PE20000329A1 (es) | 2000-04-13 |
| DK1057813T3 (da) | 2004-08-16 |
| AU766088B2 (en) | 2003-10-09 |
| ZA991590B (en) | 1999-08-27 |
| NO20004277D0 (no) | 2000-08-25 |
| CN1291976A (zh) | 2001-04-18 |
| CN1157375C (zh) | 2004-07-14 |
| NZ506497A (en) | 2004-12-24 |
| ES2220043T3 (es) | 2004-12-01 |
| DE69916586D1 (de) | 2004-05-27 |
| TWI249525B (en) | 2006-02-21 |
| US6310086B1 (en) | 2001-10-30 |
| AU2547899A (en) | 1999-09-15 |
| EP1057813A4 (en) | 2001-11-21 |
| JP4342101B2 (ja) | 2009-10-14 |
| PL342477A1 (en) | 2001-06-04 |
| HUP0100680A3 (en) | 2001-09-28 |
| DE69916586T2 (de) | 2004-09-16 |
| BR9908301A (pt) | 2000-10-31 |
| ATE264841T1 (de) | 2004-05-15 |
| EP1057813B1 (en) | 2004-04-21 |
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