CN1158299C - 取代的4-苄基氨基喹啉、其制备方法、含有这些化合物的药物及其应用 - Google Patents
取代的4-苄基氨基喹啉、其制备方法、含有这些化合物的药物及其应用 Download PDFInfo
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- CN1158299C CN1158299C CNB008131554A CN00813155A CN1158299C CN 1158299 C CN1158299 C CN 1158299C CN B008131554 A CNB008131554 A CN B008131554A CN 00813155 A CN00813155 A CN 00813155A CN 1158299 C CN1158299 C CN 1158299C
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- Prior art keywords
- methyl
- alkyl
- compound
- dimethyl
- acid
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 72
- 238000000034 method Methods 0.000 title claims abstract description 42
- 239000003814 drug Substances 0.000 title claims abstract description 8
- IEIBZPOWNOCCAT-UHFFFAOYSA-N n-benzylquinolin-4-amine Chemical compound C=1C=NC2=CC=CC=C2C=1NCC1=CC=CC=C1 IEIBZPOWNOCCAT-UHFFFAOYSA-N 0.000 title abstract description 3
- 239000003613 bile acid Substances 0.000 title description 3
- HSINOMROUCMIEA-FGVHQWLLSA-N (2s,4r)-4-[(3r,5s,6r,7r,8s,9s,10s,13r,14s,17r)-6-ethyl-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl]-2-methylpentanoic acid Chemical compound C([C@@]12C)C[C@@H](O)C[C@H]1[C@@H](CC)[C@@H](O)[C@@H]1[C@@H]2CC[C@]2(C)[C@@H]([C@H](C)C[C@H](C)C(O)=O)CC[C@H]21 HSINOMROUCMIEA-FGVHQWLLSA-N 0.000 title 1
- 150000003839 salts Chemical class 0.000 claims abstract description 19
- 239000001257 hydrogen Substances 0.000 claims description 31
- 229910052739 hydrogen Inorganic materials 0.000 claims description 31
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 25
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 24
- 229910052731 fluorine Inorganic materials 0.000 claims description 23
- 239000000203 mixture Substances 0.000 claims description 23
- 238000002360 preparation method Methods 0.000 claims description 21
- 238000006243 chemical reaction Methods 0.000 claims description 14
- 229910052801 chlorine Inorganic materials 0.000 claims description 13
- 150000002431 hydrogen Chemical class 0.000 claims description 6
- 241000282326 Felis catus Species 0.000 claims description 4
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- 238000009472 formulation Methods 0.000 claims description 3
- 229910052740 iodine Inorganic materials 0.000 claims description 3
- 239000003937 drug carrier Substances 0.000 claims description 2
- 208000001130 gallstones Diseases 0.000 abstract description 9
- 201000001883 cholelithiasis Diseases 0.000 abstract description 8
- 239000000543 intermediate Substances 0.000 description 71
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 46
- 238000000524 positive electrospray ionisation mass spectrometry Methods 0.000 description 37
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 30
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 29
- 238000002844 melting Methods 0.000 description 29
- 230000008018 melting Effects 0.000 description 29
- 239000000047 product Substances 0.000 description 28
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 27
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 27
- 239000007787 solid Substances 0.000 description 26
- 239000000243 solution Substances 0.000 description 26
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
- 230000000694 effects Effects 0.000 description 22
- 239000002253 acid Substances 0.000 description 21
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 20
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 18
- -1 or is CN Inorganic materials 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 238000007429 general method Methods 0.000 description 15
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 15
- YFGFFNPPTDOYLI-UHFFFAOYSA-N 1-(4-amino-2-methyl-3-quinolinyl)ethanone Chemical compound C1=CC=CC2=C(N)C(C(=O)C)=C(C)N=C21 YFGFFNPPTDOYLI-UHFFFAOYSA-N 0.000 description 14
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 14
- 239000002904 solvent Substances 0.000 description 14
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 12
- 238000000354 decomposition reaction Methods 0.000 description 12
- 238000004992 fast atom bombardment mass spectroscopy Methods 0.000 description 12
- 125000000217 alkyl group Chemical group 0.000 description 11
- 239000002585 base Substances 0.000 description 11
- 210000000941 bile Anatomy 0.000 description 10
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 9
- 239000011737 fluorine Substances 0.000 description 9
- 238000003756 stirring Methods 0.000 description 9
- 238000010626 work up procedure Methods 0.000 description 9
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- 150000001555 benzenes Chemical class 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 8
- 239000000872 buffer Substances 0.000 description 8
- 238000005984 hydrogenation reaction Methods 0.000 description 8
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 8
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 8
- JTSSQFSQKKVLGG-UHFFFAOYSA-N 1-[4-[(4-bromophenyl)methylamino]-2-methylquinolin-3-yl]ethanone Chemical compound CC(=O)C1=C(C)N=C2C=CC=CC2=C1NCC1=CC=C(Br)C=C1 JTSSQFSQKKVLGG-UHFFFAOYSA-N 0.000 description 7
- 235000012000 cholesterol Nutrition 0.000 description 7
- 239000012074 organic phase Substances 0.000 description 7
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N Valeric acid Natural products CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 6
- FPQVGDGSRVMNMR-JCTPKUEWSA-N [[(z)-(1-cyano-2-ethoxy-2-oxoethylidene)amino]oxy-(dimethylamino)methylidene]-dimethylazanium;tetrafluoroborate Chemical compound F[B-](F)(F)F.CCOC(=O)C(\C#N)=N/OC(N(C)C)=[N+](C)C FPQVGDGSRVMNMR-JCTPKUEWSA-N 0.000 description 6
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 6
- 235000019341 magnesium sulphate Nutrition 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- 239000003826 tablet Substances 0.000 description 6
- YLRBJYMANQKEAW-UHFFFAOYSA-N 1-bromo-4-(bromomethyl)benzene Chemical compound BrCC1=CC=C(Br)C=C1 YLRBJYMANQKEAW-UHFFFAOYSA-N 0.000 description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 239000004480 active ingredient Substances 0.000 description 5
- 150000001340 alkali metals Chemical class 0.000 description 5
- 150000004702 methyl esters Chemical class 0.000 description 5
- GBCAVSYHPPARHX-UHFFFAOYSA-M n'-cyclohexyl-n-[2-(4-methylmorpholin-4-ium-4-yl)ethyl]methanediimine;4-methylbenzenesulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1.C1CCCCC1N=C=NCC[N+]1(C)CCOCC1 GBCAVSYHPPARHX-UHFFFAOYSA-M 0.000 description 5
- 239000002244 precipitate Substances 0.000 description 5
- 238000011084 recovery Methods 0.000 description 5
- 239000000741 silica gel Substances 0.000 description 5
- 229910002027 silica gel Inorganic materials 0.000 description 5
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 4
- OCLAXAXHBFDNES-UHFFFAOYSA-N CC1=C(CC2=NC3=CC=CC=C3C=C2C(=O)O)C=CC(=C1)N Chemical compound CC1=C(CC2=NC3=CC=CC=C3C=C2C(=O)O)C=CC(=C1)N OCLAXAXHBFDNES-UHFFFAOYSA-N 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000008346 aqueous phase Substances 0.000 description 4
- 150000001768 cations Chemical group 0.000 description 4
- 239000012043 crude product Substances 0.000 description 4
- 238000010265 fast atom bombardment Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- IKDSWDBQIXGGQC-UHFFFAOYSA-N methyl 4-amino-2-methylquinoline-3-carboxylate Chemical compound C1=CC=CC2=C(N)C(C(=O)OC)=C(C)N=C21 IKDSWDBQIXGGQC-UHFFFAOYSA-N 0.000 description 4
- HNBDRPTVWVGKBR-UHFFFAOYSA-N methyl pentanoate Chemical compound CCCCC(=O)OC HNBDRPTVWVGKBR-UHFFFAOYSA-N 0.000 description 4
- 239000008194 pharmaceutical composition Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 4
- XRNVSPDQTPVECU-UHFFFAOYSA-N (4-bromophenyl)methanamine Chemical compound NCC1=CC=C(Br)C=C1 XRNVSPDQTPVECU-UHFFFAOYSA-N 0.000 description 3
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 3
- BRYUDDQHRCJNDG-UHFFFAOYSA-N 1-[4-[(3-bromophenyl)methylamino]-2-methylquinolin-3-yl]ethanone Chemical compound CC(=O)C1=C(C)N=C2C=CC=CC2=C1NCC1=CC=CC(Br)=C1 BRYUDDQHRCJNDG-UHFFFAOYSA-N 0.000 description 3
- JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 3
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 3
- 239000007995 HEPES buffer Substances 0.000 description 3
- 229910006069 SO3H Inorganic materials 0.000 description 3
- DTQVDTLACAAQTR-UHFFFAOYSA-M Trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-M 0.000 description 3
- 229910001413 alkali metal ion Inorganic materials 0.000 description 3
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 description 3
- 150000005010 aminoquinolines Chemical class 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
- MFMCYGKKSRZQME-UHFFFAOYSA-N butyl 4-[(4-bromophenyl)methylamino]-2-methylquinoline-3-carboxylate Chemical compound CCCCOC(=O)C1=C(C)N=C2C=CC=CC2=C1NCC1=CC=C(Br)C=C1 MFMCYGKKSRZQME-UHFFFAOYSA-N 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- BHQCQFFYRZLCQQ-OELDTZBJSA-N cholic acid Chemical compound C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(O)=O)C)[C@@]2(C)[C@@H](O)C1 BHQCQFFYRZLCQQ-OELDTZBJSA-N 0.000 description 3
- 238000004587 chromatography analysis Methods 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000008103 glucose Substances 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- NPZTUJOABDZTLV-UHFFFAOYSA-N hydroxybenzotriazole Substances O=C1C=CC=C2NNN=C12 NPZTUJOABDZTLV-UHFFFAOYSA-N 0.000 description 3
- FSQDAABCVFLUMV-UHFFFAOYSA-N methyl 4-[(4-bromophenyl)methylamino]-2-methylquinoline-3-carboxylate Chemical compound COC(=O)C1=C(C)N=C2C=CC=CC2=C1NCC1=CC=C(Br)C=C1 FSQDAABCVFLUMV-UHFFFAOYSA-N 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 229940002612 prodrug Drugs 0.000 description 3
- 239000000651 prodrug Substances 0.000 description 3
- OQBAIRDLKWKOGY-UHFFFAOYSA-N propan-2-yl 4-[(4-bromophenyl)methylamino]-2-methylquinoline-3-carboxylate Chemical compound CC(C)OC(=O)C1=C(C)N=C2C=CC=CC2=C1NCC1=CC=C(Br)C=C1 OQBAIRDLKWKOGY-UHFFFAOYSA-N 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- 125000001453 quaternary ammonium group Chemical group 0.000 description 3
- 238000010898 silica gel chromatography Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- VNOBMNRGROUYAL-UHFFFAOYSA-N 1-(4-chloro-2,6-dimethylpyridin-3-yl)ethanone Chemical compound CC(=O)C1=C(C)N=C(C)C=C1Cl VNOBMNRGROUYAL-UHFFFAOYSA-N 0.000 description 2
- HOKRBUVXBKUFSZ-UHFFFAOYSA-N 1-[4-[(4-bromo-2-chlorophenyl)methylamino]-2-methylquinolin-3-yl]ethanone Chemical compound CC(=O)C1=C(C)N=C2C=CC=CC2=C1NCC1=CC=C(Br)C=C1Cl HOKRBUVXBKUFSZ-UHFFFAOYSA-N 0.000 description 2
- GRXNBRLNCVAYKD-UHFFFAOYSA-N 1-[4-[(4-bromo-2-fluorophenyl)methylamino]-2-methylquinolin-3-yl]ethanone Chemical compound CC(=O)C1=C(C)N=C2C=CC=CC2=C1NCC1=CC=C(Br)C=C1F GRXNBRLNCVAYKD-UHFFFAOYSA-N 0.000 description 2
- LBMZTEXHLALCLK-UHFFFAOYSA-N 1-[4-[(4-bromo-3-chlorophenyl)methylamino]-2-methylquinolin-3-yl]ethanone Chemical compound CC(=O)C1=C(C)N=C2C=CC=CC2=C1NCC1=CC=C(Br)C(Cl)=C1 LBMZTEXHLALCLK-UHFFFAOYSA-N 0.000 description 2
- NQMQTVLHRMBTQW-UHFFFAOYSA-N 1-[4-[(4-bromo-3-fluorophenyl)methylamino]-2-methylquinolin-3-yl]ethanone Chemical compound CC(=O)C1=C(C)N=C2C=CC=CC2=C1NCC1=CC=C(Br)C(F)=C1 NQMQTVLHRMBTQW-UHFFFAOYSA-N 0.000 description 2
- VVLDZAOFLUCDQS-UHFFFAOYSA-N 1-[4-[(4-bromophenyl)methylamino]-2,6-dimethylpyridin-3-yl]ethanone Chemical compound CC(=O)C1=C(C)N=C(C)C=C1NCC1=CC=C(Br)C=C1 VVLDZAOFLUCDQS-UHFFFAOYSA-N 0.000 description 2
- PVTZVZWUSBMRMH-UHFFFAOYSA-N 1-[4-[(4-bromophenyl)methylamino]-6-ethyl-2-methylpyridin-3-yl]ethanone Chemical compound CC1=NC(CC)=CC(NCC=2C=CC(Br)=CC=2)=C1C(C)=O PVTZVZWUSBMRMH-UHFFFAOYSA-N 0.000 description 2
- JMHQMRVQXICDKM-UHFFFAOYSA-N 2-(4-oxopent-2-en-2-ylamino)benzonitrile Chemical compound CC(=O)C=C(C)NC1=CC=CC=C1C#N JMHQMRVQXICDKM-UHFFFAOYSA-N 0.000 description 2
- HLCPWBZNUKCSBN-UHFFFAOYSA-N 2-aminobenzonitrile Chemical compound NC1=CC=CC=C1C#N HLCPWBZNUKCSBN-UHFFFAOYSA-N 0.000 description 2
- YXNMZAQIYBATAT-UHFFFAOYSA-N 4-(benzylamino)-2-methylquinoline-3-carboxylic acid Chemical compound OC(=O)C=1C(C)=NC2=CC=CC=C2C=1NCC1=CC=CC=C1 YXNMZAQIYBATAT-UHFFFAOYSA-N 0.000 description 2
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 2
- JLLYLQLDYORLBB-UHFFFAOYSA-N 5-bromo-n-methylthiophene-2-sulfonamide Chemical compound CNS(=O)(=O)C1=CC=C(Br)S1 JLLYLQLDYORLBB-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 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 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 229930006000 Sucrose Natural products 0.000 description 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 230000004071 biological effect Effects 0.000 description 2
- 244000309464 bull Species 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 229940099352 cholate Drugs 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 125000004494 ethyl ester group Chemical group 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 210000000232 gallbladder Anatomy 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 230000003834 intracellular effect Effects 0.000 description 2
- 239000007937 lozenge Substances 0.000 description 2
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- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- FKHIFSZMMVMEQY-UHFFFAOYSA-N talc Chemical compound [Mg+2].[O-][Si]([O-])=O FKHIFSZMMVMEQY-UHFFFAOYSA-N 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- WHRNULOCNSKMGB-UHFFFAOYSA-N tetrahydrofuran thf Chemical compound C1CCOC1.C1CCOC1 WHRNULOCNSKMGB-UHFFFAOYSA-N 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J43/00—Normal steroids having a nitrogen-containing hetero ring spiro-condensed or not condensed with the cyclopenta(a)hydrophenanthrene skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J43/00—Normal steroids having a nitrogen-containing hetero ring spiro-condensed or not condensed with the cyclopenta(a)hydrophenanthrene skeleton
- C07J43/003—Normal steroids having a nitrogen-containing hetero ring spiro-condensed or not condensed with the cyclopenta(a)hydrophenanthrene skeleton not condensed
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J41/00—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring
- C07J41/0033—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005
- C07J41/0055—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005 the 17-beta position being substituted by an uninterrupted chain of at least three carbon atoms which may or may not be branched, e.g. cholane or cholestane derivatives, optionally cyclised, e.g. 17-beta-phenyl or 17-beta-furyl derivatives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J41/00—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring
- C07J41/0033—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005
- C07J41/0055—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005 the 17-beta position being substituted by an uninterrupted chain of at least three carbon atoms which may or may not be branched, e.g. cholane or cholestane derivatives, optionally cyclised, e.g. 17-beta-phenyl or 17-beta-furyl derivatives
- C07J41/0061—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005 the 17-beta position being substituted by an uninterrupted chain of at least three carbon atoms which may or may not be branched, e.g. cholane or cholestane derivatives, optionally cyclised, e.g. 17-beta-phenyl or 17-beta-furyl derivatives one of the carbon atoms being part of an amide group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J9/00—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane
- C07J9/005—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane containing a carboxylic function directly attached or attached by a chain containing only carbon atoms to the cyclopenta[a]hydrophenanthrene skeleton
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Obesity (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Gastroenterology & Hepatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Steroid Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Quinoline Compounds (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1999145385 DE19945385A1 (de) | 1999-09-22 | 1999-09-22 | Substituierte 4-Benzylaminochinoline und ihre Heteroanlagen, Verfahren zu ihrer Herstellung, diese Verbindungen enthaltende Arzneimittel und deren Verwendung |
| DE19945385.343 | 1999-09-22 | ||
| DE2000128193 DE10028193A1 (de) | 2000-06-09 | 2000-06-09 | Substituierte 4-Benzylamminochinoline und ihre Heteroanalogen, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikamente oder Diagnostika, sowie sie enthaltende Medikamente |
| DE10028193.1 | 2000-06-09 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1374968A CN1374968A (zh) | 2002-10-16 |
| CN1158299C true CN1158299C (zh) | 2004-07-21 |
Family
ID=26005994
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB008131554A Expired - Fee Related CN1158299C (zh) | 1999-09-22 | 2000-09-06 | 取代的4-苄基氨基喹啉、其制备方法、含有这些化合物的药物及其应用 |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US6339077B1 (enExample) |
| EP (1) | EP1218401B1 (enExample) |
| JP (1) | JP4833471B2 (enExample) |
| KR (1) | KR20030010575A (enExample) |
| CN (1) | CN1158299C (enExample) |
| AT (1) | ATE269352T1 (enExample) |
| AU (1) | AU779412B2 (enExample) |
| BR (1) | BR0014233A (enExample) |
| CA (1) | CA2385445A1 (enExample) |
| CZ (1) | CZ2002992A3 (enExample) |
| DE (1) | DE50006842D1 (enExample) |
| DK (1) | DK1218401T3 (enExample) |
| EE (1) | EE200200143A (enExample) |
| ES (1) | ES2218222T3 (enExample) |
| HK (1) | HK1049169B (enExample) |
| HR (1) | HRP20020238A2 (enExample) |
| HU (1) | HUP0203045A3 (enExample) |
| IL (1) | IL148739A0 (enExample) |
| NO (1) | NO20021337L (enExample) |
| NZ (1) | NZ517899A (enExample) |
| PL (1) | PL353992A1 (enExample) |
| PT (1) | PT1218401E (enExample) |
| RU (1) | RU2247125C2 (enExample) |
| SK (1) | SK3862002A3 (enExample) |
| WO (1) | WO2001021642A1 (enExample) |
| YU (1) | YU19302A (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6576644B2 (en) | 2000-09-06 | 2003-06-10 | Bristol-Myers Squibb Co. | Quinoline inhibitors of cGMP phosphodiesterase |
| ITMI20021025A1 (it) * | 2002-05-14 | 2003-11-14 | Nicox Sa | Farmaci per il trattamento acuto di disfunzioni del circolo venoso epatico e portale |
| CZ301037B6 (cs) * | 2007-09-06 | 2009-10-21 | Vysoká škola chemicko-technologická v Praze | Amidové konjugáty steroidních a žlucových kyselin s D-glukosaminem a zpusob jejich prípravy |
| JP5744003B2 (ja) * | 2009-03-24 | 2015-07-01 | アッヴィ・バハマズ・リミテッド | 抗ウイルス化合物を調製する方法 |
| CA2792068A1 (en) * | 2010-04-02 | 2011-10-06 | Senomyx, Inc. | Sweet flavor modifier |
| MY179876A (en) | 2011-08-12 | 2020-11-18 | Firmenich Incorporated | Sweet flavor modifier |
| US11339128B2 (en) | 2014-11-07 | 2022-05-24 | Firmenich Incorporated | Substituted 4-amino-5-(cyclohexyloxy)quinoline-3-carboxylic acids as sweet flavor modifiers |
| US12186329B2 (en) | 2018-08-23 | 2025-01-07 | President And Fellows Of Harvard College | Compositions and methods related to cholic acid 7-sulfate as a treatment for diabetes |
| EP3890745B1 (en) | 2018-12-04 | 2025-11-19 | President and Fellows of Harvard College | Synthetic derivatives of cholic acid 7-sulfate and uses thereof |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4789678A (en) * | 1986-08-25 | 1988-12-06 | Hoechst-Roussel Pharmaceuticals, Inc. | Memory enhancing α-alkyl-4-amino-3-quinolinemethanols and 1-(4-aralkylamino-3-quinolinyl)alkanones and related compounds |
| JPH0667846B2 (ja) * | 1989-04-28 | 1994-08-31 | 一 滝川 | 利胆剤 |
| IT1259419B (it) * | 1991-05-24 | 1996-03-18 | Erba Carlo Spa | Steroidi 3-carbossi 17b - sostituiti insaturi utili come inibitori della testosterone 5 a reduttasi |
| TW289021B (enExample) | 1993-05-08 | 1996-10-21 | Hoechst Ag | |
| IT1274000B (it) * | 1994-04-06 | 1997-07-14 | Alfa Wassermann Spa | Derivati di acidi biliari utili nella terapia della calcolosi biliare da colesterolo e nelle patologie indotte da colestasi |
| DE4432708A1 (de) | 1994-09-14 | 1996-03-21 | Hoechst Ag | Modifizierte Gallensäuren, Verfahren zu ihrer Herstellung und ihre Verwendung |
| JPH09315979A (ja) * | 1996-05-24 | 1997-12-09 | Tokyo Tanabe Co Ltd | 利胆剤 |
| WO1998056757A1 (fr) * | 1997-06-11 | 1998-12-17 | Sankyo Company, Limited | Derives de benzylamine |
-
2000
- 2000-09-06 AU AU75156/00A patent/AU779412B2/en not_active Ceased
- 2000-09-06 AT AT00964126T patent/ATE269352T1/de not_active IP Right Cessation
- 2000-09-06 HR HR20020238A patent/HRP20020238A2/xx not_active Application Discontinuation
- 2000-09-06 DK DK00964126T patent/DK1218401T3/da active
- 2000-09-06 PT PT00964126T patent/PT1218401E/pt unknown
- 2000-09-06 IL IL14873900A patent/IL148739A0/xx unknown
- 2000-09-06 JP JP2001525216A patent/JP4833471B2/ja not_active Expired - Fee Related
- 2000-09-06 EE EEP200200143A patent/EE200200143A/xx unknown
- 2000-09-06 WO PCT/EP2000/008691 patent/WO2001021642A1/de not_active Ceased
- 2000-09-06 CZ CZ2002992A patent/CZ2002992A3/cs unknown
- 2000-09-06 KR KR1020027003757A patent/KR20030010575A/ko not_active Ceased
- 2000-09-06 HU HU0203045A patent/HUP0203045A3/hu unknown
- 2000-09-06 CN CNB008131554A patent/CN1158299C/zh not_active Expired - Fee Related
- 2000-09-06 SK SK386-2002A patent/SK3862002A3/sk unknown
- 2000-09-06 NZ NZ517899A patent/NZ517899A/en unknown
- 2000-09-06 BR BR0014233-6A patent/BR0014233A/pt not_active IP Right Cessation
- 2000-09-06 RU RU2002110440/04A patent/RU2247125C2/ru not_active IP Right Cessation
- 2000-09-06 CA CA002385445A patent/CA2385445A1/en not_active Abandoned
- 2000-09-06 ES ES00964126T patent/ES2218222T3/es not_active Expired - Lifetime
- 2000-09-06 HK HK03101156.5A patent/HK1049169B/zh not_active IP Right Cessation
- 2000-09-06 YU YU19302A patent/YU19302A/sh unknown
- 2000-09-06 DE DE50006842T patent/DE50006842D1/de not_active Expired - Lifetime
- 2000-09-06 EP EP00964126A patent/EP1218401B1/de not_active Expired - Lifetime
- 2000-09-06 PL PL00353992A patent/PL353992A1/xx not_active Application Discontinuation
- 2000-09-22 US US09/667,668 patent/US6339077B1/en not_active Expired - Lifetime
-
2002
- 2002-03-18 NO NO20021337A patent/NO20021337L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| EE200200143A (et) | 2003-04-15 |
| NO20021337D0 (no) | 2002-03-18 |
| PL353992A1 (en) | 2003-12-15 |
| YU19302A (sh) | 2004-11-25 |
| SK3862002A3 (en) | 2003-01-09 |
| CA2385445A1 (en) | 2001-03-29 |
| DE50006842D1 (de) | 2004-07-22 |
| PT1218401E (pt) | 2004-10-29 |
| EP1218401A1 (de) | 2002-07-03 |
| HK1049169A1 (en) | 2003-05-02 |
| JP4833471B2 (ja) | 2011-12-07 |
| KR20030010575A (ko) | 2003-02-05 |
| ES2218222T3 (es) | 2004-11-16 |
| HK1049169B (zh) | 2005-04-22 |
| US6339077B1 (en) | 2002-01-15 |
| AU779412B2 (en) | 2005-01-20 |
| HUP0203045A3 (en) | 2004-06-28 |
| EP1218401B1 (de) | 2004-06-16 |
| JP2003510255A (ja) | 2003-03-18 |
| HRP20020238A2 (en) | 2004-04-30 |
| IL148739A0 (en) | 2002-09-12 |
| NO20021337L (no) | 2002-05-15 |
| NZ517899A (en) | 2004-03-26 |
| RU2247125C2 (ru) | 2005-02-27 |
| WO2001021642A1 (de) | 2001-03-29 |
| CZ2002992A3 (cs) | 2002-06-12 |
| BR0014233A (pt) | 2002-05-21 |
| DK1218401T3 (da) | 2004-10-04 |
| HUP0203045A2 (hu) | 2003-01-28 |
| ATE269352T1 (de) | 2004-07-15 |
| AU7515600A (en) | 2001-04-24 |
| CN1374968A (zh) | 2002-10-16 |
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