NO316666B1 - Kinolonkarboksylsyrederivater eller deres salter - Google Patents
Kinolonkarboksylsyrederivater eller deres salter Download PDFInfo
- Publication number
- NO316666B1 NO316666B1 NO19983625A NO983625A NO316666B1 NO 316666 B1 NO316666 B1 NO 316666B1 NO 19983625 A NO19983625 A NO 19983625A NO 983625 A NO983625 A NO 983625A NO 316666 B1 NO316666 B1 NO 316666B1
- Authority
- NO
- Norway
- Prior art keywords
- salt
- compound
- general formula
- dihydro
- cyclopropyl
- Prior art date
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- 150000003839 salts Chemical class 0.000 title claims abstract description 134
- XOQQVKDBGLYPGH-UHFFFAOYSA-N 2-oxo-1h-quinoline-3-carboxylic acid Chemical class C1=CC=C2NC(=O)C(C(=O)O)=CC2=C1 XOQQVKDBGLYPGH-UHFFFAOYSA-N 0.000 title claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 13
- 125000005843 halogen group Chemical group 0.000 claims abstract description 12
- 239000002253 acid Substances 0.000 claims abstract description 10
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 15
- 238000004519 manufacturing process Methods 0.000 claims description 13
- 238000002360 preparation method Methods 0.000 claims description 6
- IBGWUWYVISOKHY-UHFFFAOYSA-N 1-cyclopropyl-7-(2,3-dihydro-1h-isoindol-5-yl)-8-methoxy-4-oxoquinoline-3-carboxylic acid Chemical compound COC1=C(C=2C=C3CNCC3=CC=2)C=CC(C(C(C(O)=O)=C2)=O)=C1N2C1CC1 IBGWUWYVISOKHY-UHFFFAOYSA-N 0.000 claims description 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 5
- 239000003242 anti bacterial agent Substances 0.000 claims description 4
- RATIWBOHUIFHIJ-UHFFFAOYSA-N 1-cyclopropyl-8-(difluoromethoxy)-7-(2,3-dihydro-1h-isoindol-5-yl)-4-oxoquinoline-3-carboxylic acid Chemical compound C12=C(OC(F)F)C(C=3C=C4CNCC4=CC=3)=CC=C2C(=O)C(C(=O)O)=CN1C1CC1 RATIWBOHUIFHIJ-UHFFFAOYSA-N 0.000 claims description 3
- LWJLLBOVJVEMCG-UHFFFAOYSA-N 1-cyclopropyl-8-methoxy-7-(1-methyl-2,3-dihydro-1h-isoindol-5-yl)-4-oxoquinoline-3-carboxylic acid Chemical compound COC1=C(C=2C=C3CNC(C)C3=CC=2)C=CC(C(C(C(O)=O)=C2)=O)=C1N2C1CC1 LWJLLBOVJVEMCG-UHFFFAOYSA-N 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 239000000825 pharmaceutical preparation Substances 0.000 claims description 2
- 150000007660 quinolones Chemical class 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 abstract description 153
- 239000001257 hydrogen Substances 0.000 abstract description 5
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 3
- 150000002431 hydrogen Chemical class 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 125000005346 substituted cycloalkyl group Chemical group 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 66
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 51
- 239000000203 mixture Substances 0.000 description 50
- 239000000243 solution Substances 0.000 description 49
- 239000002904 solvent Substances 0.000 description 49
- 238000006243 chemical reaction Methods 0.000 description 40
- 239000012044 organic layer Substances 0.000 description 37
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 36
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 36
- 239000011541 reaction mixture Substances 0.000 description 36
- 239000013078 crystal Substances 0.000 description 35
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 34
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 31
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 30
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 30
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 30
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 30
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 26
- 238000000034 method Methods 0.000 description 25
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 24
- 230000000052 comparative effect Effects 0.000 description 22
- 238000001914 filtration Methods 0.000 description 21
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 20
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 18
- 238000004440 column chromatography Methods 0.000 description 18
- -1 methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy Chemical group 0.000 description 17
- 229920006395 saturated elastomer Polymers 0.000 description 17
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 16
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 16
- 239000003480 eluent Substances 0.000 description 16
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 15
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 15
- 239000011780 sodium chloride Substances 0.000 description 15
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 13
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 12
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 10
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 10
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000003054 catalyst Substances 0.000 description 9
- 230000000694 effects Effects 0.000 description 9
- 239000012046 mixed solvent Substances 0.000 description 9
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 8
- 150000001408 amides Chemical class 0.000 description 8
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 8
- FUOXHFDFJCMFRA-UHFFFAOYSA-N ethyl 2-(4-bromo-2-fluoro-3-methylbenzoyl)-3-(cyclopropylamino)prop-2-enoate Chemical compound C=1C=C(Br)C(C)=C(F)C=1C(=O)C(C(=O)OCC)=CNC1CC1 FUOXHFDFJCMFRA-UHFFFAOYSA-N 0.000 description 8
- 238000010992 reflux Methods 0.000 description 8
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 8
- 238000001816 cooling Methods 0.000 description 7
- 229910052763 palladium Inorganic materials 0.000 description 7
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 6
- NJDRXTDGYFKORP-UHFFFAOYSA-N 1-cyclopropyl-8-(difluoromethoxy)-7-(1-methyl-2,3-dihydro-1h-isoindol-2-ium-5-yl)-4-oxoquinoline-3-carboxylate Chemical compound C=1C=C2C(C)NCC2=CC=1C(C=1OC(F)F)=CC=C(C(C(C(O)=O)=C2)=O)C=1N2C1CC1 NJDRXTDGYFKORP-UHFFFAOYSA-N 0.000 description 6
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 6
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 6
- 239000002585 base Substances 0.000 description 6
- 239000003921 oil Substances 0.000 description 6
- 229910000027 potassium carbonate Inorganic materials 0.000 description 6
- 125000006239 protecting group Chemical group 0.000 description 6
- 239000008096 xylene Substances 0.000 description 6
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 5
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 5
- 239000012298 atmosphere Substances 0.000 description 5
- 239000001569 carbon dioxide Substances 0.000 description 5
- 229910002092 carbon dioxide Inorganic materials 0.000 description 5
- 150000002170 ethers Chemical class 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- AGILTSYHCGBVTG-UHFFFAOYSA-N 6-bromo-4-fluoro-2-(4-methylphenyl)sulfonyl-1,3-dihydroisoindole Chemical compound C1=CC(C)=CC=C1S(=O)(=O)N1CC2=C(F)C=C(Br)C=C2C1 AGILTSYHCGBVTG-UHFFFAOYSA-N 0.000 description 4
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 4
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 4
- 230000000844 anti-bacterial effect Effects 0.000 description 4
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 4
- 150000001721 carbon Chemical group 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- PFKFTWBEEFSNDU-UHFFFAOYSA-N carbonyldiimidazole Chemical compound C1=CN=CN1C(=O)N1C=CN=C1 PFKFTWBEEFSNDU-UHFFFAOYSA-N 0.000 description 4
- MYSWGUAQZAJSOK-UHFFFAOYSA-N ciprofloxacin Chemical compound C12=CC(N3CCNCC3)=C(F)C=C2C(=O)C(C(=O)O)=CN1C1CC1 MYSWGUAQZAJSOK-UHFFFAOYSA-N 0.000 description 4
- 238000005859 coupling reaction Methods 0.000 description 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 4
- 239000000706 filtrate Substances 0.000 description 4
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 4
- 239000005457 ice water Substances 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 4
- 239000012299 nitrogen atmosphere Substances 0.000 description 4
- 150000002905 orthoesters Chemical class 0.000 description 4
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 4
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
- PYOKUURKVVELLB-UHFFFAOYSA-N trimethyl orthoformate Chemical compound COC(OC)OC PYOKUURKVVELLB-UHFFFAOYSA-N 0.000 description 4
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 3
- RRQYJINTUHWNHW-UHFFFAOYSA-N 1-ethoxy-2-(2-ethoxyethoxy)ethane Chemical compound CCOCCOCCOCC RRQYJINTUHWNHW-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 3
- ZSXGLVDWWRXATF-UHFFFAOYSA-N N,N-dimethylformamide dimethyl acetal Chemical compound COC(OC)N(C)C ZSXGLVDWWRXATF-UHFFFAOYSA-N 0.000 description 3
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 3
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 3
- UTYPOJCVSLXTNI-UHFFFAOYSA-N benzyl 5-bromo-1-methyl-1,3-dihydroisoindole-2-carboxylate Chemical compound C1C2=CC(Br)=CC=C2C(C)N1C(=O)OCC1=CC=CC=C1 UTYPOJCVSLXTNI-UHFFFAOYSA-N 0.000 description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000012230 colorless oil Substances 0.000 description 3
- 229940019778 diethylene glycol diethyl ether Drugs 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 150000004673 fluoride salts Chemical class 0.000 description 3
- 150000004820 halides Chemical class 0.000 description 3
- 150000008282 halocarbons Chemical class 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 159000000003 magnesium salts Chemical class 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 238000007363 ring formation reaction Methods 0.000 description 3
- 239000012312 sodium hydride Substances 0.000 description 3
- 229910000104 sodium hydride Inorganic materials 0.000 description 3
- 239000012453 solvate Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 150000003462 sulfoxides Chemical class 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- IPJALOIDFYMFEI-UHFFFAOYSA-N (1-methyl-2-trityl-1,3-dihydroisoindol-5-yl)boronic acid Chemical compound C1C2=CC(B(O)O)=CC=C2C(C)N1C(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 IPJALOIDFYMFEI-UHFFFAOYSA-N 0.000 description 2
- IOBWAHRFIPQEQL-UHFFFAOYSA-N 1,3-difluoro-2-methoxybenzene Chemical compound COC1=C(F)C=CC=C1F IOBWAHRFIPQEQL-UHFFFAOYSA-N 0.000 description 2
- DBKLLRRNCRZSOE-UHFFFAOYSA-N 1-cyclopropyl-7-(7-fluoro-2,3-dihydro-1h-isoindol-5-yl)-8-methoxy-4-oxoquinoline-3-carboxylic acid Chemical compound COC1=C(C=2C=C(F)C=3CNCC=3C=2)C=CC(C(C(C(O)=O)=C2)=O)=C1N2C1CC1 DBKLLRRNCRZSOE-UHFFFAOYSA-N 0.000 description 2
- NBPVDGXTPQMTRT-UHFFFAOYSA-N 1-cyclopropyl-8-(difluoromethoxy)-7-(2-methyl-1,3-dihydroisoindol-5-yl)-4-oxoquinoline-3-carboxylic acid Chemical compound C1=C2CN(C)CC2=CC=C1C(C=1OC(F)F)=CC=C(C(C(C(O)=O)=C2)=O)C=1N2C1CC1 NBPVDGXTPQMTRT-UHFFFAOYSA-N 0.000 description 2
- KOGXAHZNANLRJB-UHFFFAOYSA-N 1-cyclopropyl-8-(difluoromethoxy)-7-(7-fluoro-2,3-dihydro-1h-isoindol-5-yl)-4-oxoquinoline-3-carboxylic acid Chemical compound C12=C(OC(F)F)C(C=3C=C(F)C=4CNCC=4C=3)=CC=C2C(=O)C(C(=O)O)=CN1C1CC1 KOGXAHZNANLRJB-UHFFFAOYSA-N 0.000 description 2
- RFAMJZMMUAKZDX-UHFFFAOYSA-N 1-cyclopropyl-8-methoxy-4-oxo-7-(2-phenylmethoxycarbonyl-1,3-dihydroisoindol-5-yl)quinoline-3-carboxylic acid Chemical compound COC1=C(C=2C=C3CN(CC3=CC=2)C(=O)OCC=2C=CC=CC=2)C=CC(C(C(C(O)=O)=C2)=O)=C1N2C1CC1 RFAMJZMMUAKZDX-UHFFFAOYSA-N 0.000 description 2
- WSHHAIYKQTYWNU-UHFFFAOYSA-N 1-cyclopropyl-8-methoxy-7-(2-methyl-1,3-dihydroisoindol-5-yl)-4-oxoquinoline-3-carboxylic acid Chemical compound COC1=C(C=2C=C3CN(C)CC3=CC=2)C=CC(C(C(C(O)=O)=C2)=O)=C1N2C1CC1 WSHHAIYKQTYWNU-UHFFFAOYSA-N 0.000 description 2
- PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- ODKRCZFHARCFGI-UHFFFAOYSA-N 4-amino-2-fluoro-3-methylbenzoic acid Chemical compound CC1=C(N)C=CC(C(O)=O)=C1F ODKRCZFHARCFGI-UHFFFAOYSA-N 0.000 description 2
- PJYGXPFKKAJUBG-UHFFFAOYSA-N 4-bromo-1,2-bis(bromomethyl)benzene Chemical compound BrCC1=CC=C(Br)C=C1CBr PJYGXPFKKAJUBG-UHFFFAOYSA-N 0.000 description 2
- PIMDCUNZRUXGME-UHFFFAOYSA-N 4-bromo-2-fluoro-3-methylbenzoic acid Chemical compound CC1=C(Br)C=CC(C(O)=O)=C1F PIMDCUNZRUXGME-UHFFFAOYSA-N 0.000 description 2
- ILNJBIQQAIIMEY-UHFFFAOYSA-N 4-oxo-1h-quinoline-3-carboxylic acid Chemical compound C1=CC=CC2=C(O)C(C(=O)O)=CN=C21 ILNJBIQQAIIMEY-UHFFFAOYSA-N 0.000 description 2
- VYPQVSNICHCXLF-UHFFFAOYSA-N 5-bromo-1,2-bis(bromomethyl)-3-fluorobenzene Chemical compound FC1=CC(Br)=CC(CBr)=C1CBr VYPQVSNICHCXLF-UHFFFAOYSA-N 0.000 description 2
- ZMXJBSZYQBRDSC-UHFFFAOYSA-N 5-bromo-1-fluoro-2,3-dimethylbenzene Chemical compound CC1=CC(Br)=CC(F)=C1C ZMXJBSZYQBRDSC-UHFFFAOYSA-N 0.000 description 2
- HUWRJTHKCYGECM-UHFFFAOYSA-N 5-bromo-1-methyl-2-trityl-1,3-dihydroisoindole Chemical compound C1C2=CC(Br)=CC=C2C(C)N1C(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 HUWRJTHKCYGECM-UHFFFAOYSA-N 0.000 description 2
- BVFKMKMJQJDOPR-UHFFFAOYSA-N 5-bromo-2,3-dimethylaniline Chemical compound CC1=CC(Br)=CC(N)=C1C BVFKMKMJQJDOPR-UHFFFAOYSA-N 0.000 description 2
- OSTUUSSBUJMYGX-UHFFFAOYSA-N 5-bromo-2-(4-methylphenyl)sulfonyl-1,3-dihydroisoindole Chemical compound C1=CC(C)=CC=C1S(=O)(=O)N1CC2=CC(Br)=CC=C2C1 OSTUUSSBUJMYGX-UHFFFAOYSA-N 0.000 description 2
- TTZVRIQURVPHRS-UHFFFAOYSA-N 5-bromo-6-fluoro-2-(4-methylphenyl)sulfonyl-1,3-dihydroisoindole Chemical compound C1=CC(C)=CC=C1S(=O)(=O)N1CC2=CC(Br)=C(F)C=C2C1 TTZVRIQURVPHRS-UHFFFAOYSA-N 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
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- RJQXTJLFIWVMTO-TYNCELHUSA-N Methicillin Chemical compound COC1=CC=CC(OC)=C1C(=O)N[C@@H]1C(=O)N2[C@@H](C(O)=O)C(C)(C)S[C@@H]21 RJQXTJLFIWVMTO-TYNCELHUSA-N 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
- PHSPJQZRQAJPPF-UHFFFAOYSA-N N-alpha-Methylhistamine Chemical compound CNCCC1=CN=CN1 PHSPJQZRQAJPPF-UHFFFAOYSA-N 0.000 description 1
- 101100030361 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) pph-3 gene Proteins 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 238000000297 Sandmeyer reaction Methods 0.000 description 1
- 241000191967 Staphylococcus aureus Species 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- OKJPEAGHQZHRQV-UHFFFAOYSA-N Triiodomethane Natural products IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- 101100020289 Xenopus laevis koza gene Proteins 0.000 description 1
- GFQKHXCSNFITHX-UHFFFAOYSA-N [4-bromo-2-(hydroxymethyl)phenyl]methanol Chemical compound OCC1=CC=C(Br)C=C1CO GFQKHXCSNFITHX-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- JUHORIMYRDESRB-UHFFFAOYSA-N benzathine Chemical compound C=1C=CC=CC=1CNCCNCC1=CC=CC=C1 JUHORIMYRDESRB-UHFFFAOYSA-N 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- LZCLZPXCOKSFNU-UHFFFAOYSA-N benzyl 5-bromo-1,3-dihydroisoindole-2-carboxylate Chemical compound C1C2=CC(Br)=CC=C2CN1C(=O)OCC1=CC=CC=C1 LZCLZPXCOKSFNU-UHFFFAOYSA-N 0.000 description 1
- MPTRETZZNQDVMV-UHFFFAOYSA-N benzyl 5-tributylstannyl-1,3-dihydroisoindole-2-carboxylate Chemical compound C1C2=CC([Sn](CCCC)(CCCC)CCCC)=CC=C2CN1C(=O)OCC1=CC=CC=C1 MPTRETZZNQDVMV-UHFFFAOYSA-N 0.000 description 1
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 1
- YNHIGQDRGKUECZ-UHFFFAOYSA-L bis(triphenylphosphine)palladium(ii) dichloride Chemical compound [Cl-].[Cl-].[Pd+2].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 YNHIGQDRGKUECZ-UHFFFAOYSA-L 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical group 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000006285 cell suspension Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000002512 chemotherapy Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 238000006114 decarboxylation reaction Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 description 1
- BGRWYRAHAFMIBJ-UHFFFAOYSA-N diisopropylcarbodiimide Natural products CC(C)NC(=O)NC(C)C BGRWYRAHAFMIBJ-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- RKHHTKKGOSHEGG-UHFFFAOYSA-N ethyl 1-cyclopropyl-7-[4-fluoro-2-(4-methylphenyl)sulfonyl-1,3-dihydroisoindol-5-yl]-8-methoxy-4-oxoquinoline-3-carboxylate Chemical compound C12=C(OC)C(C=3C(=C4CN(CC4=CC=3)S(=O)(=O)C=3C=CC(C)=CC=3)F)=CC=C2C(=O)C(C(=O)OCC)=CN1C1CC1 RKHHTKKGOSHEGG-UHFFFAOYSA-N 0.000 description 1
- RZPJIURYCHAGHQ-UHFFFAOYSA-N ethyl 1-cyclopropyl-7-[6-fluoro-2-(4-methylphenyl)sulfonyl-1,3-dihydroisoindol-5-yl]-8-methoxy-4-oxoquinoline-3-carboxylate Chemical compound C12=C(OC)C(C=3C(=CC=4CN(CC=4C=3)S(=O)(=O)C=3C=CC(C)=CC=3)F)=CC=C2C(=O)C(C(=O)OCC)=CN1C1CC1 RZPJIURYCHAGHQ-UHFFFAOYSA-N 0.000 description 1
- IGAGFONHXAICGW-UHFFFAOYSA-N ethyl 1-cyclopropyl-8-(difluoromethoxy)-7-(1-methyl-2-phenylmethoxycarbonyl-1,3-dihydroisoindol-5-yl)-4-oxoquinoline-3-carboxylate Chemical compound C12=C(OC(F)F)C(C=3C=C4CN(C(C)C4=CC=3)C(=O)OCC=3C=CC=CC=3)=CC=C2C(=O)C(C(=O)OCC)=CN1C1CC1 IGAGFONHXAICGW-UHFFFAOYSA-N 0.000 description 1
- DDEXFWPIKLVUNL-UHFFFAOYSA-N ethyl 1-cyclopropyl-8-(difluoromethoxy)-7-(1-methyl-2-trityl-1,3-dihydroisoindol-5-yl)-4-oxoquinoline-3-carboxylate Chemical compound C12=C(OC(F)F)C(C=3C=C4CN(C(C)C4=CC=3)C(C=3C=CC=CC=3)(C=3C=CC=CC=3)C=3C=CC=CC=3)=CC=C2C(=O)C(C(=O)OCC)=CN1C1CC1 DDEXFWPIKLVUNL-UHFFFAOYSA-N 0.000 description 1
- PBFYSZQITWVSKS-UHFFFAOYSA-N ethyl 1-cyclopropyl-8-(difluoromethoxy)-7-[2-(4-methylphenyl)sulfonyl-1,3-dihydroisoindol-5-yl]-4-oxoquinoline-3-carboxylate Chemical compound C12=C(OC(F)F)C(C=3C=C4CN(CC4=CC=3)S(=O)(=O)C=3C=CC(C)=CC=3)=CC=C2C(=O)C(C(=O)OCC)=CN1C1CC1 PBFYSZQITWVSKS-UHFFFAOYSA-N 0.000 description 1
- VABWCPUTLWAXNL-UHFFFAOYSA-N ethyl 2,4-difluoro-3-methylbenzoate Chemical compound CCOC(=O)C1=CC=C(F)C(C)=C1F VABWCPUTLWAXNL-UHFFFAOYSA-N 0.000 description 1
- ANRNSRWKIQLFSW-UHFFFAOYSA-N ethyl 7-bromo-1-cyclopropyl-4-oxo-8-(trifluoromethyl)quinoline-3-carboxylate Chemical compound C12=C(C(F)(F)F)C(Br)=CC=C2C(=O)C(C(=O)OCC)=CN1C1CC1 ANRNSRWKIQLFSW-UHFFFAOYSA-N 0.000 description 1
- WSECQYQYXDBJMT-UHFFFAOYSA-N ethyl 7-bromo-1-cyclopropyl-8-fluoro-4-oxoquinoline-3-carboxylate Chemical compound C12=C(F)C(Br)=CC=C2C(=O)C(C(=O)OCC)=CN1C1CC1 WSECQYQYXDBJMT-UHFFFAOYSA-N 0.000 description 1
- OSIFVNCLXWXPNL-UHFFFAOYSA-N ethyl 7-bromo-8-chloro-1-cyclopropyl-4-oxoquinoline-3-carboxylate Chemical compound C12=C(Cl)C(Br)=CC=C2C(=O)C(C(=O)OCC)=CN1C1CC1 OSIFVNCLXWXPNL-UHFFFAOYSA-N 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000002140 halogenating effect Effects 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 238000006138 lithiation reaction Methods 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- DVWUPYHFVYOPNV-UHFFFAOYSA-L magnesium;3-ethoxy-3-oxopropanoate Chemical compound [Mg+2].CCOC(=O)CC([O-])=O.CCOC(=O)CC([O-])=O DVWUPYHFVYOPNV-UHFFFAOYSA-L 0.000 description 1
- UKVIEHSSVKSQBA-UHFFFAOYSA-N methane;palladium Chemical compound C.[Pd] UKVIEHSSVKSQBA-UHFFFAOYSA-N 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- CEYPKILZGDCHIX-UHFFFAOYSA-N methyl 3-(difluoromethoxy)-2,4-difluorobenzoate Chemical compound COC(=O)C1=CC=C(F)C(OC(F)F)=C1F CEYPKILZGDCHIX-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229960003085 meticillin Drugs 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- OGJPXUAPXNRGGI-UHFFFAOYSA-N norfloxacin Chemical compound C1=C2N(CC)C=C(C(O)=O)C(=O)C2=CC(F)=C1N1CCNCC1 OGJPXUAPXNRGGI-UHFFFAOYSA-N 0.000 description 1
- 229960001180 norfloxacin Drugs 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 229960001699 ofloxacin Drugs 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 1
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011698 potassium fluoride Substances 0.000 description 1
- 235000003270 potassium fluoride Nutrition 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- MFDFERRIHVXMIY-UHFFFAOYSA-N procaine Chemical compound CCN(CC)CCOC(=O)C1=CC=C(N)C=C1 MFDFERRIHVXMIY-UHFFFAOYSA-N 0.000 description 1
- 229960004919 procaine Drugs 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229910001923 silver oxide Inorganic materials 0.000 description 1
- 239000011775 sodium fluoride Substances 0.000 description 1
- 235000013024 sodium fluoride Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- GXTGJNPFAHSYJW-UHFFFAOYSA-N tributyl-[2-(4-methylphenyl)sulfonyl-1,3-dihydroisoindol-5-yl]stannane Chemical compound C1C2=CC([Sn](CCCC)(CCCC)CCCC)=CC=C2CN1S(=O)(=O)C1=CC=C(C)C=C1 GXTGJNPFAHSYJW-UHFFFAOYSA-N 0.000 description 1
- MLTFTYCEGVOGQO-UHFFFAOYSA-N tributyl-[4-fluoro-2-(4-methylphenyl)sulfonyl-1,3-dihydroisoindol-5-yl]stannane Chemical compound C1C2=C(F)C([Sn](CCCC)(CCCC)CCCC)=CC=C2CN1S(=O)(=O)C1=CC=C(C)C=C1 MLTFTYCEGVOGQO-UHFFFAOYSA-N 0.000 description 1
- WURBUUCFBKUKMZ-UHFFFAOYSA-N tributyl-[7-methoxy-2-(4-methylphenyl)sulfonyl-1,3-dihydroisoindol-5-yl]stannane Chemical compound C1C=2C(OC)=CC([Sn](CCCC)(CCCC)CCCC)=CC=2CN1S(=O)(=O)C1=CC=C(C)C=C1 WURBUUCFBKUKMZ-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- DTQVDTLACAAQTR-DYCDLGHISA-N trifluoroacetic acid-d1 Chemical compound [2H]OC(=O)C(F)(F)F DTQVDTLACAAQTR-DYCDLGHISA-N 0.000 description 1
- JBWKIWSBJXDJDT-UHFFFAOYSA-N triphenylmethyl chloride Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 JBWKIWSBJXDJDT-UHFFFAOYSA-N 0.000 description 1
- NHDIQVFFNDKAQU-UHFFFAOYSA-N tripropan-2-yl borate Chemical compound CC(C)OB(OC(C)C)OC(C)C NHDIQVFFNDKAQU-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/475—Quinolines; Isoquinolines having an indole ring, e.g. yohimbine, reserpine, strychnine, vinblastine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/025—Boronic and borinic acid compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Quinoline Compounds (AREA)
- Indole Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4793696 | 1996-02-09 | ||
| PCT/JP1997/000317 WO1997029102A1 (fr) | 1996-02-09 | 1997-02-07 | Derives de l'acide quinolonecarboxylique et leurs sels |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO983625D0 NO983625D0 (no) | 1998-08-07 |
| NO983625L NO983625L (no) | 1998-08-07 |
| NO316666B1 true NO316666B1 (no) | 2004-03-29 |
Family
ID=12789268
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19983625A NO316666B1 (no) | 1996-02-09 | 1998-08-07 | Kinolonkarboksylsyrederivater eller deres salter |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US6025370A (zh) |
| EP (1) | EP0882725B1 (zh) |
| KR (1) | KR100276477B1 (zh) |
| CN (2) | CN100395244C (zh) |
| AT (1) | ATE229950T1 (zh) |
| AU (1) | AU711914B2 (zh) |
| CA (1) | CA2242242C (zh) |
| DE (1) | DE69717970T2 (zh) |
| DK (1) | DK0882725T3 (zh) |
| ES (1) | ES2188890T3 (zh) |
| HK (1) | HK1039118B (zh) |
| HU (1) | HU228567B1 (zh) |
| IL (1) | IL124944A (zh) |
| NO (1) | NO316666B1 (zh) |
| NZ (1) | NZ330775A (zh) |
| PT (1) | PT882725E (zh) |
| WO (1) | WO1997029102A1 (zh) |
| ZA (1) | ZA971023B (zh) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR9812644B1 (pt) | 1997-09-15 | 2010-07-13 | quinolonas antimicrobianas, composição farmacêutica e uso das mesmas. | |
| US6387928B1 (en) | 1997-09-15 | 2002-05-14 | The Procter & Gamble Co. | Antimicrobial quinolones, their compositions and uses |
| TW593308B (en) * | 1997-10-27 | 2004-06-21 | Toyama Chemical Co Ltd | Processes for producing 7-isoindoline-quinolonecarboxylic acid derivative and its intermediate |
| PT1070713E (pt) * | 1998-04-06 | 2006-12-29 | Toyama Chemical Co Ltd | Derivados de ácido quinolonocarboxílico ou seus sais |
| JP4499846B2 (ja) * | 1998-05-07 | 2010-07-07 | 富山化学工業株式会社 | ７−イソインドリン−キノロンカルボン酸誘導体の製造法並びにイソインドリン−５−ボロン酸誘導体の製造法 |
| JP4549461B2 (ja) * | 1998-08-31 | 2010-09-22 | 富山化学工業株式会社 | ７−ブロモ−キノロンカルボン酸誘導体の製造法 |
| JP2000229946A (ja) * | 1998-12-10 | 2000-08-22 | Toyama Chem Co Ltd | キノロンカルボン酸の製造法およびその中間体 |
| JP4694669B2 (ja) | 1999-03-17 | 2011-06-08 | 第一三共株式会社 | 医薬組成物 |
| JP4619658B2 (ja) | 2002-03-12 | 2011-01-26 | 富山化学工業株式会社 | 快い味の経口懸濁液および方法 |
| EP1634879A4 (en) * | 2003-06-19 | 2007-09-05 | Daiichi Seiyaku Co | METHOD FOR THE SELECTIVE INTRODUCTION OF AN AMINO SUBSTITUENT |
| KR100981351B1 (ko) * | 2003-10-29 | 2010-09-10 | 주식회사 엘지생명과학 | 7-클로로-1-사이클로프로필-6-플루오로-4-옥소-1,4-디하이드로-1,8-나프티리딘-3-카복실산의 제조방법 |
| US20090156577A1 (en) * | 2004-09-09 | 2009-06-18 | Benjamin Davis | 7-amino alkylidenyl-heterocyclic quinolones and naphthyridones |
| CN101133009B (zh) * | 2005-03-03 | 2012-05-09 | Jnc株式会社 | 氯氟苯液晶化合物、液晶组成物及液晶显示元件 |
| KR20110082635A (ko) | 2006-03-28 | 2011-07-19 | 워너 칠콧 컴퍼니 엘엘씨 | 퀴놀론 중간체를 제조하기 위한 커플링 방법 |
| BRPI0709209A2 (pt) | 2006-03-28 | 2011-06-28 | Procter & Gamble | processo de redução de hidreto para preparo de intermediários de quinolona |
| US7902227B2 (en) * | 2007-07-27 | 2011-03-08 | Janssen Pharmaceutica Nv. | C-7 isoxazolinyl quinolone / naphthyridine derivatives useful as antibacterial agents |
| CN101298418B (zh) * | 2008-06-13 | 2010-12-15 | 江苏康鹏农化有限公司 | 3-氧代-3-(2,4-二卤代-3-二氟甲氧基苯基)丙酸乙酯的制备方法 |
| CN102212056A (zh) * | 2010-04-09 | 2011-10-12 | 山东轩竹医药科技有限公司 | 新的双环喹诺酮类化合物 |
| WO2013121439A2 (en) * | 2012-02-15 | 2013-08-22 | Glenmark Generics Limited | Process for garenoxacin mesylate |
| BR112015023044A8 (pt) | 2013-03-15 | 2021-09-28 | Melinta Subsidiary Corp | Métodos para tratar infecções em pacientes acima do peso e obesos com o uso de antibióticos |
| GB201516614D0 (en) * | 2015-09-18 | 2015-11-04 | Redx Pharma Plc | Antibacterial compounds |
| CN105837555B (zh) * | 2016-03-31 | 2019-01-25 | 南京华威医药科技集团有限公司 | 加雷沙星及其中间体制备方法 |
| CN111620901B (zh) * | 2020-06-08 | 2023-03-21 | 蚌埠医学院第二附属医院 | 一种含硅氧烷基的氟喹诺酮化合物、其制备方法及用途 |
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| JPS6199835A (ja) * | 1984-10-22 | 1986-05-17 | Shimadzu Corp | 振動試験機の波形補正装置 |
| MY105136A (en) * | 1988-04-27 | 1994-08-30 | Daiichi Seiyaku Co | Optically active pyridonecarboxylic acid derivatives. |
| WO1991002526A1 (en) * | 1989-08-16 | 1991-03-07 | Pfizer Inc. | Azabicyclo quinolone carboxylic acids |
| EG20543A (en) * | 1992-10-30 | 1999-07-31 | Procter & Gamble | Process for preparing of novel antimicrobial -5- (n-heterosubstituted amino) quinolones |
| JPH07300472A (ja) * | 1992-12-28 | 1995-11-14 | Korea Res Inst Chem Technol | 新規キノロンカルボン酸誘導体およびその製造方法 |
| JPH06199835A (ja) * | 1993-01-08 | 1994-07-19 | Hokuriku Seiyaku Co Ltd | ８−ジフルオロメトキシキノリン−３−カルボン酸誘導体 |
| DE4301246A1 (de) * | 1993-01-19 | 1994-07-21 | Bayer Ag | Chinolon- und Naphthyridoncarbonsäurederivate |
| JPH0848629A (ja) * | 1994-08-08 | 1996-02-20 | Dainippon Pharmaceut Co Ltd | ピリドンカルボン酸誘導体およびそれを有効成分とする抗ピロリ菌剤 |
| HU228062B1 (en) * | 1994-08-12 | 2012-09-28 | Toyama Chemical Co Ltd | Quinolone- carboxylic acid derivative and salt thereof |
-
1997
- 1997-02-07 CN CNB011012323A patent/CN100395244C/zh not_active Expired - Lifetime
- 1997-02-07 EP EP97902618A patent/EP0882725B1/en not_active Expired - Lifetime
- 1997-02-07 IL IL12494497A patent/IL124944A/xx not_active IP Right Cessation
- 1997-02-07 DK DK97902618T patent/DK0882725T3/da active
- 1997-02-07 PT PT97902618T patent/PT882725E/pt unknown
- 1997-02-07 CA CA002242242A patent/CA2242242C/en not_active Expired - Lifetime
- 1997-02-07 ZA ZA9701023A patent/ZA971023B/xx unknown
- 1997-02-07 HU HU9901966A patent/HU228567B1/hu unknown
- 1997-02-07 KR KR1019980706138A patent/KR100276477B1/ko not_active IP Right Cessation
- 1997-02-07 US US09/125,016 patent/US6025370A/en not_active Expired - Lifetime
- 1997-02-07 ES ES97902618T patent/ES2188890T3/es not_active Expired - Lifetime
- 1997-02-07 NZ NZ330775A patent/NZ330775A/xx not_active IP Right Cessation
- 1997-02-07 AT AT97902618T patent/ATE229950T1/de active
- 1997-02-07 DE DE69717970T patent/DE69717970T2/de not_active Expired - Lifetime
- 1997-02-07 CN CN97192130A patent/CN1100053C/zh not_active Expired - Lifetime
- 1997-02-07 WO PCT/JP1997/000317 patent/WO1997029102A1/ja active IP Right Grant
- 1997-02-07 AU AU16701/97A patent/AU711914B2/en not_active Expired
-
1998
- 1998-08-07 NO NO19983625A patent/NO316666B1/no not_active IP Right Cessation
-
2002
- 2002-01-16 HK HK02100336.1A patent/HK1039118B/zh not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| HU228567B1 (en) | 2013-04-29 |
| NZ330775A (en) | 1999-08-30 |
| CN100395244C (zh) | 2008-06-18 |
| EP0882725A4 (en) | 1999-05-06 |
| KR100276477B1 (ko) | 2000-12-15 |
| CA2242242C (en) | 2001-08-07 |
| EP0882725A1 (en) | 1998-12-09 |
| US6025370A (en) | 2000-02-15 |
| IL124944A0 (en) | 1999-01-26 |
| CN1314355A (zh) | 2001-09-26 |
| CN1100053C (zh) | 2003-01-29 |
| DK0882725T3 (da) | 2003-01-13 |
| ATE229950T1 (de) | 2003-01-15 |
| EP0882725B1 (en) | 2002-12-18 |
| AU1670197A (en) | 1997-08-28 |
| ES2188890T3 (es) | 2003-07-01 |
| DE69717970T2 (de) | 2003-04-30 |
| AU711914B2 (en) | 1999-10-21 |
| CA2242242A1 (en) | 1997-08-14 |
| HK1039118A1 (en) | 2002-04-12 |
| PT882725E (pt) | 2003-04-30 |
| DE69717970D1 (de) | 2003-01-30 |
| NO983625D0 (no) | 1998-08-07 |
| IL124944A (en) | 2003-06-24 |
| HUP9901966A3 (en) | 2002-01-28 |
| HUP9901966A2 (hu) | 1999-09-28 |
| KR19990082406A (ko) | 1999-11-25 |
| ZA971023B (en) | 1997-09-25 |
| CN1210533A (zh) | 1999-03-10 |
| NO983625L (no) | 1998-08-07 |
| HK1039118B (zh) | 2009-01-30 |
| WO1997029102A1 (fr) | 1997-08-14 |
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| MK1K | Patent expired |