SE504625C2 - Pyridonkarboxylsyraderivat och salter därav, förfarande för deras framställning samt antibakteriella medel innehållande dessa - Google Patents
Pyridonkarboxylsyraderivat och salter därav, förfarande för deras framställning samt antibakteriella medel innehållande dessaInfo
- Publication number
- SE504625C2 SE504625C2 SE8901464A SE8901464A SE504625C2 SE 504625 C2 SE504625 C2 SE 504625C2 SE 8901464 A SE8901464 A SE 8901464A SE 8901464 A SE8901464 A SE 8901464A SE 504625 C2 SE504625 C2 SE 504625C2
- Authority
- SE
- Sweden
- Prior art keywords
- group
- carboxylic acid
- groups
- lower alkyl
- benzoxazine
- Prior art date
Links
- 150000003839 salts Chemical class 0.000 title claims abstract description 138
- YSLIPUSJNFIFAB-UHFFFAOYSA-N 2-oxopyridine-1-carboxylic acid Chemical class OC(=O)N1C=CC=CC1=O YSLIPUSJNFIFAB-UHFFFAOYSA-N 0.000 title claims abstract description 30
- 238000000034 method Methods 0.000 title claims abstract description 20
- 230000008569 process Effects 0.000 title claims abstract description 16
- 238000002360 preparation method Methods 0.000 title claims description 18
- 239000003242 anti bacterial agent Substances 0.000 title abstract description 4
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims abstract description 10
- 238000004519 manufacturing process Methods 0.000 claims abstract description 3
- 239000000203 mixture Substances 0.000 claims description 132
- 150000001875 compounds Chemical class 0.000 claims description 125
- -1 1-aminocyclopropyl Chemical group 0.000 claims description 79
- 125000000217 alkyl group Chemical group 0.000 claims description 77
- 125000003282 alkyl amino group Chemical group 0.000 claims description 37
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 36
- 125000003277 amino group Chemical group 0.000 claims description 30
- XNIVKSPSCYJKBL-UHFFFAOYSA-N 2h-1,2-benzoxazine-6-carboxylic acid Chemical compound O1NC=CC2=CC(C(=O)O)=CC=C21 XNIVKSPSCYJKBL-UHFFFAOYSA-N 0.000 claims description 22
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 21
- 125000005843 halogen group Chemical group 0.000 claims description 21
- CFLBIADORGSMCX-UHFFFAOYSA-N 2h-1,4-benzoxazine-6-carboxylic acid Chemical compound O1CC=NC2=CC(C(=O)O)=CC=C21 CFLBIADORGSMCX-UHFFFAOYSA-N 0.000 claims description 20
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 18
- 125000006239 protecting group Chemical group 0.000 claims description 17
- 230000000844 anti-bacterial effect Effects 0.000 claims description 13
- 125000001118 alkylidene group Chemical group 0.000 claims description 9
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 9
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052760 oxygen Inorganic materials 0.000 claims description 7
- 239000001301 oxygen Substances 0.000 claims description 7
- 229910052717 sulfur Inorganic materials 0.000 claims description 7
- 125000004434 sulfur atom Chemical group 0.000 claims description 7
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 229910001512 metal fluoride Inorganic materials 0.000 claims description 6
- 238000007363 ring formation reaction Methods 0.000 claims description 6
- 229910052731 fluorine Inorganic materials 0.000 claims description 5
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims description 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- 239000003814 drug Substances 0.000 claims description 4
- 125000001153 fluoro group Chemical group F* 0.000 claims description 4
- 125000001841 imino group Chemical group [H]N=* 0.000 claims description 4
- XAGMUUZPGZWTRP-ZETCQYMHSA-N LSM-5745 Chemical compound C([C@@H](N1C2=C(C(C(C(O)=O)=C1)=O)C=C1F)C)OC2=C1C1(N)CC1 XAGMUUZPGZWTRP-ZETCQYMHSA-N 0.000 claims description 2
- 208000022362 bacterial infectious disease Diseases 0.000 claims description 2
- 150000005130 benzoxazines Chemical class 0.000 claims description 2
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 238000006467 substitution reaction Methods 0.000 claims description 2
- 125000005189 alkyl hydroxy group Chemical group 0.000 claims 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims 3
- RMYXASXFLAOBMO-QMMMGPOBSA-N (2S)-6-(1-aminocyclopropyl)-2-ethyl-7-fluoro-10-oxo-4-oxa-1-azatricyclo[7.3.1.05,13]trideca-5(13),6,8,11-tetraene-11-carboxylic acid Chemical compound C([C@@H](N1C2=C(C(C(C(O)=O)=C1)=O)C=C1F)CC)OC2=C1C1(N)CC1 RMYXASXFLAOBMO-QMMMGPOBSA-N 0.000 claims 2
- XAGMUUZPGZWTRP-UHFFFAOYSA-N 7H-Pyrido(1,2,3-de)-1,4-benzoxazine-6-carboxylic acid, 2,3-dihydro-10-(1-aminocyclopropyl)-9-fluoro-3-methyl-7-oxo- Chemical compound FC1=CC(C(C(C(O)=O)=C2)=O)=C3N2C(C)COC3=C1C1(N)CC1 XAGMUUZPGZWTRP-UHFFFAOYSA-N 0.000 claims 2
- QLUCKWIJEFIBNH-UHFFFAOYSA-N FC1=C(F)C(C(C(C(O)=O)=C2)=O)=C3N2C(C)COC3=C1C1(N)CC1 Chemical compound FC1=C(F)C(C(C(C(O)=O)=C2)=O)=C3N2C(C)COC3=C1C1(N)CC1 QLUCKWIJEFIBNH-UHFFFAOYSA-N 0.000 claims 2
- HSIAQCPCYWQOMF-UHFFFAOYSA-N FC1=C(O)C(C(C(C(O)=O)=C2)=O)=C3N2C(C)COC3=C1C1(N)CC1 Chemical compound FC1=C(O)C(C(C(C(O)=O)=C2)=O)=C3N2C(C)COC3=C1C1(N)CC1 HSIAQCPCYWQOMF-UHFFFAOYSA-N 0.000 claims 2
- JNKURAJOPQTQEI-UHFFFAOYSA-N FC=1C=C(C(C(C(O)=O)=CN2C(=C)CO3)=O)C2=C3C=1C1(N)CC1 Chemical compound FC=1C=C(C(C(C(O)=O)=CN2C(=C)CO3)=O)C2=C3C=1C1(N)CC1 JNKURAJOPQTQEI-UHFFFAOYSA-N 0.000 claims 2
- 125000001589 carboacyl group Chemical group 0.000 claims 2
- AAAVFYXUSXVEJV-DSUYNRRISA-N (2S)-6-(1-amino-2-methylcyclopropyl)-7-fluoro-2-methyl-10-oxo-4-oxa-1-azatricyclo[7.3.1.05,13]trideca-5(13),6,8,11-tetraene-11-carboxylic acid Chemical compound CC1CC1(N)C1=C(F)C=C2C(=O)C(C(O)=O)=CN3[C@@H](C)COC1=C32 AAAVFYXUSXVEJV-DSUYNRRISA-N 0.000 claims 1
- PVTXJGJDOHYFOX-UHFFFAOYSA-N 2h-1,4-benzoxazine Chemical compound C1=CC=C2N=CCOC2=C1 PVTXJGJDOHYFOX-UHFFFAOYSA-N 0.000 claims 1
- DNUJVGBNIXGTHC-UHFFFAOYSA-N 3,6-dihydro-2h-oxazine Chemical compound C1NOCC=C1 DNUJVGBNIXGTHC-UHFFFAOYSA-N 0.000 claims 1
- GIQPGLZDVHMFLK-UHFFFAOYSA-N FC1=C(N)C(C(C(C(O)=O)=C2)=O)=C3N2C(C)COC3=C1C1(N)CC1 Chemical compound FC1=C(N)C(C(C(C(O)=O)=C2)=O)=C3N2C(C)COC3=C1C1(N)CC1 GIQPGLZDVHMFLK-UHFFFAOYSA-N 0.000 claims 1
- GAEOCRHMZVHDMN-UHFFFAOYSA-N FC=1C=C(C(C(C(O)=O)=CN2C(CF)CO3)=O)C2=C3C=1C1(N)CC1 Chemical compound FC=1C=C(C(C(C(O)=O)=CN2C(CF)CO3)=O)C2=C3C=1C1(N)CC1 GAEOCRHMZVHDMN-UHFFFAOYSA-N 0.000 claims 1
- 102100021243 G-protein coupled receptor 182 Human genes 0.000 claims 1
- 101001040797 Homo sapiens G-protein coupled receptor 182 Proteins 0.000 claims 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000005907 alkyl ester group Chemical group 0.000 claims 1
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims 1
- 229940124597 therapeutic agent Drugs 0.000 claims 1
- SQMFHXCAROIIPN-UHFFFAOYSA-N 2h-pyrido[2,3-h][1,2]benzothiazine Chemical group C1=CC2=NC=CC=C2C2=C1C=CNS2 SQMFHXCAROIIPN-UHFFFAOYSA-N 0.000 abstract 1
- QDEJGQKJMKXYLM-UHFFFAOYSA-N 2h-pyrido[2,3-h][1,2]benzoxazine Chemical group C1=CC2=NC=CC=C2C2=C1C=CNO2 QDEJGQKJMKXYLM-UHFFFAOYSA-N 0.000 abstract 1
- ZIAQCYZPKDIKRM-UHFFFAOYSA-N pyrido[3,2-f]quinoxaline Chemical group C1=CN=C2C3=CC=CN=C3C=CC2=N1 ZIAQCYZPKDIKRM-UHFFFAOYSA-N 0.000 abstract 1
- 235000002639 sodium chloride Nutrition 0.000 description 146
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 125
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 99
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 72
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 68
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 64
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 60
- 239000011541 reaction mixture Substances 0.000 description 59
- 239000000243 solution Substances 0.000 description 58
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 55
- 239000002904 solvent Substances 0.000 description 55
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 50
- 239000012047 saturated solution Substances 0.000 description 38
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 37
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 35
- 238000004821 distillation Methods 0.000 description 34
- 239000012044 organic layer Substances 0.000 description 34
- 239000011780 sodium chloride Substances 0.000 description 34
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 33
- 238000006243 chemical reaction Methods 0.000 description 33
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 28
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 28
- 238000001816 cooling Methods 0.000 description 26
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 24
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 24
- 238000004440 column chromatography Methods 0.000 description 22
- 239000013078 crystal Substances 0.000 description 20
- 239000003480 eluent Substances 0.000 description 20
- 238000001914 filtration Methods 0.000 description 20
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 16
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 16
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 12
- 239000002585 base Substances 0.000 description 12
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 12
- 239000012312 sodium hydride Substances 0.000 description 12
- 229910000104 sodium hydride Inorganic materials 0.000 description 12
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 10
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 9
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 8
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 8
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 8
- 238000002844 melting Methods 0.000 description 8
- 230000008018 melting Effects 0.000 description 8
- 235000017557 sodium bicarbonate Nutrition 0.000 description 8
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 8
- 239000000725 suspension Substances 0.000 description 8
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 8
- FCYFNNCOWAGAGQ-UHFFFAOYSA-N 2h-1,2-benzoxazine-6-carboxylic acid;hydrochloride Chemical compound Cl.O1NC=CC2=CC(C(=O)O)=CC=C21 FCYFNNCOWAGAGQ-UHFFFAOYSA-N 0.000 description 7
- 150000001408 amides Chemical class 0.000 description 7
- 238000006114 decarboxylation reaction Methods 0.000 description 7
- 231100000989 no adverse effect Toxicity 0.000 description 7
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- PFKFTWBEEFSNDU-UHFFFAOYSA-N carbonyldiimidazole Chemical compound C1=CN=CN1C(=O)N1C=CN=C1 PFKFTWBEEFSNDU-UHFFFAOYSA-N 0.000 description 6
- 238000010511 deprotection reaction Methods 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 241000894006 Bacteria Species 0.000 description 5
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 229910000027 potassium carbonate Inorganic materials 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-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
- PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 150000002170 ethers Chemical class 0.000 description 4
- 150000004820 halides Chemical class 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 238000006722 reduction reaction Methods 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 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
- 238000011282 treatment Methods 0.000 description 4
- JABYJIQOLGWMQW-UHFFFAOYSA-N undec-4-ene Chemical compound CCCCCCC=CCCC JABYJIQOLGWMQW-UHFFFAOYSA-N 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 3
- NPKFQMSURLLUON-UHFFFAOYSA-N 1-(2,3,5,6-tetrafluoro-4-methoxycarbonylphenyl)cyclopropane-1-carboxylic acid Chemical compound FC1=C(F)C(C(=O)OC)=C(F)C(F)=C1C1(C(O)=O)CC1 NPKFQMSURLLUON-UHFFFAOYSA-N 0.000 description 3
- QCRNZIUYIXDWBG-UHFFFAOYSA-N 2-(4-ethoxycarbonyl-2,3,6-trifluorophenyl)cyclopropane-1-carboxylic acid Chemical compound FC1=C(F)C(C(=O)OCC)=CC(F)=C1C1C(C(O)=O)C1 QCRNZIUYIXDWBG-UHFFFAOYSA-N 0.000 description 3
- AQNOPFHAWMMARU-UHFFFAOYSA-N 2H-1,4-benzoxazine-6-carboxylic acid hydrochloride Chemical compound Cl.O1CC=NC2=C1C=CC(=C2)C(=O)O AQNOPFHAWMMARU-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 3
- 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 3
- 239000012359 Methanesulfonyl chloride Substances 0.000 description 3
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 3
- 150000001241 acetals Chemical class 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
- 235000019445 benzyl alcohol Nutrition 0.000 description 3
- 239000002775 capsule Substances 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
- 239000000706 filtrate Substances 0.000 description 3
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 3
- 150000008282 halocarbons Chemical class 0.000 description 3
- 238000001802 infusion Methods 0.000 description 3
- 159000000003 magnesium salts Chemical class 0.000 description 3
- UKVIEHSSVKSQBA-UHFFFAOYSA-N methane;palladium Chemical compound C.[Pd] UKVIEHSSVKSQBA-UHFFFAOYSA-N 0.000 description 3
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 3
- HDEGCHZQHGTBCP-UHFFFAOYSA-N methyl 4-(3-benzhydryloxy-3-oxoprop-1-en-2-yl)-2,3,5,6-tetrafluorobenzoate Chemical compound FC1=C(F)C(C(=O)OC)=C(F)C(F)=C1C(=C)C(=O)OC(C=1C=CC=CC=1)C1=CC=CC=C1 HDEGCHZQHGTBCP-UHFFFAOYSA-N 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 description 2
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- 230000008025 crystallization Effects 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 125000006003 dichloroethyl group Chemical group 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 125000006264 diethylaminomethyl group Chemical group [H]C([H])([H])C([H])([H])N(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940019778 diethylene glycol diethyl ether Drugs 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- 125000006222 dimethylaminomethyl group Chemical group [H]C([H])([H])N(C([H])([H])[H])C([H])([H])* 0.000 description 1
- NWLKWRIHQBTKLL-UHFFFAOYSA-N ditert-butyl 2-(4-ethoxycarbonyl-2,3,6-trifluorophenyl)cyclopropane-1,1-dicarboxylate Chemical compound FC1=C(F)C(C(=O)OCC)=CC(F)=C1C1C(C(=O)OC(C)(C)C)(C(=O)OC(C)(C)C)C1 NWLKWRIHQBTKLL-UHFFFAOYSA-N 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- DZGCGKFAPXFTNM-UHFFFAOYSA-N ethanol;hydron;chloride Chemical compound Cl.CCO DZGCGKFAPXFTNM-UHFFFAOYSA-N 0.000 description 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 1
- JQXNOCGJLFMLJD-INIZCTEOSA-N ethyl (s)-10-(1-benzyloxycarbonylaminocyclopropyl)-9-fluoro-1,3-dimethyl-7-oxo-2,3-dihydro-1h,7h-pyrido[1,2,3-de]-quinoxaline-6-carboxylate Chemical compound C([C@H](C)N1C=C(C(C(=C11)C=C2F)=O)C(=O)OCC)N(C)C1=C2C1(NC(=O)OCC=2C=CC=CC=2)CC1 JQXNOCGJLFMLJD-INIZCTEOSA-N 0.000 description 1
- VKARKRMLWGMWRC-IDKOKCKLSA-N ethyl (s)-10-(2-carboxycyclopropyl)-9-fluoro-3-methyl-7-oxo-2,3-dihydro-7h-pyrido[1,2,3-de][1,4]-benzoxazine-6-carboxylate Chemical compound C([C@H](C)N1C=C(C(C(=C11)C=C2F)=O)C(=O)OCC)OC1=C2C1CC1C(O)=O VKARKRMLWGMWRC-IDKOKCKLSA-N 0.000 description 1
- JVMXBOYOJDJZJU-UHFFFAOYSA-N ethyl 10-(1-benzyloxycarbonylaminocyclopropyl)-9-fluoro-3-(2-tetrahydropyranyloxymethyl)-7-oxo-2,3-dihydro-7h-pyrido[1,2,3-de][1,4]benzoxazine-6-carboxylate Chemical compound C1OC(C2=3)=C(C4(CC4)NC(=O)OCC=4C=CC=CC=4)C(F)=CC=3C(=O)C(C(=O)OCC)=CN2C1COC1CCCCO1 JVMXBOYOJDJZJU-UHFFFAOYSA-N 0.000 description 1
- LAPLBVHPJVHUGW-UHFFFAOYSA-N ethyl 10-(1-benzyloxycarbonylaminocyclopropyl)-9-fluoro-3-fluoromethyl-7-oxo-2,3-dihydro-7h-pyrido[1,2,3-de][1,4]benzoxazine-6carboxylate Chemical compound FC1=CC(=C23)C(=O)C(C(=O)OCC)=CN2C(CF)COC3=C1C1(NC(=O)OCC=2C=CC=CC=2)CC1 LAPLBVHPJVHUGW-UHFFFAOYSA-N 0.000 description 1
- NMXRPPFZHAVRPX-UHFFFAOYSA-N ethyl 2,3,5-trifluoro-4-[2-[(2-methylpropan-2-yl)oxycarbonyl]cyclopropyl]benzoate Chemical compound FC1=C(F)C(C(=O)OCC)=CC(F)=C1C1C(C(=O)OC(C)(C)C)C1 NMXRPPFZHAVRPX-UHFFFAOYSA-N 0.000 description 1
- JPNMTELFQZIBBP-UHFFFAOYSA-N ethyl 3-(4-cyclopropyl-2,3,5,6-tetrafluorophenyl)-3-oxopropanoate Chemical compound FC1=C(F)C(C(=O)CC(=O)OCC)=C(F)C(F)=C1C1CC1 JPNMTELFQZIBBP-UHFFFAOYSA-N 0.000 description 1
- POGVTFJLAFTEHA-UHFFFAOYSA-N ethyl 3-oxo-3-[2,3,5,6-tetrafluoro-4-[1-(phenylmethoxycarbonylamino)cyclopropyl]phenyl]propanoate Chemical compound FC1=C(F)C(C(=O)CC(=O)OCC)=C(F)C(F)=C1C1(NC(=O)OCC=2C=CC=CC=2)CC1 POGVTFJLAFTEHA-UHFFFAOYSA-N 0.000 description 1
- BTBYEIRYHQRTLV-UHFFFAOYSA-N ethyl 4-(1-benzhydryloxy-1-oxobut-2-en-2-yl)-2,3,5-trifluorobenzoate Chemical compound FC1=C(F)C(C(=O)OCC)=CC(F)=C1C(=CC)C(=O)OC(C=1C=CC=CC=1)C1=CC=CC=C1 BTBYEIRYHQRTLV-UHFFFAOYSA-N 0.000 description 1
- HYBBPHVVVTXWKJ-UHFFFAOYSA-N ethyl 4-(1-benzhydryloxy-3-hydroxy-1-oxopropan-2-yl)-2,3,5-trifluorobenzoate Chemical compound FC1=C(F)C(C(=O)OCC)=CC(F)=C1C(CO)C(=O)OC(C=1C=CC=CC=1)C1=CC=CC=C1 HYBBPHVVVTXWKJ-UHFFFAOYSA-N 0.000 description 1
- GZMZDMQKOLVYSB-UHFFFAOYSA-N ethyl 4-(1-benzhydryloxycarbonyl-2-methylcyclopropyl)-2,3,5-trifluorobenzoate Chemical compound FC1=C(F)C(C(=O)OCC)=CC(F)=C1C1(C(=O)OC(C=2C=CC=CC=2)C=2C=CC=CC=2)C(C)C1 GZMZDMQKOLVYSB-UHFFFAOYSA-N 0.000 description 1
- NYNCLMXFMIYTNL-UHFFFAOYSA-N ethyl 4-(1-benzhydryloxycarbonylcyclopropyl)-2,3,5-trifluorobenzoate Chemical compound FC1=C(F)C(C(=O)OCC)=CC(F)=C1C1(C(=O)OC(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 NYNCLMXFMIYTNL-UHFFFAOYSA-N 0.000 description 1
- ORVSLHNMJRNJNK-INIZCTEOSA-N ethyl 6,8-difluoro-1-[(2s)-1-(methylamino)propan-2-yl]-4-oxo-7-[1-(phenylmethoxycarbonylamino)cyclopropyl]quinoline-3-carboxylate Chemical compound FC=1C=C2C(=O)C(C(=O)OCC)=CN([C@@H](C)CNC)C2=C(F)C=1C1(NC(=O)OCC=2C=CC=CC=2)CC1 ORVSLHNMJRNJNK-INIZCTEOSA-N 0.000 description 1
- BNFKLLOGMXXMED-IBGZPJMESA-N ethyl 6,8-difluoro-1-[(2s)-1-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]propan-2-yl]-4-oxo-7-[1-(phenylmethoxycarbonylamino)cyclopropyl]quinoline-3-carboxylate Chemical compound FC=1C=C2C(=O)C(C(=O)OCC)=CN([C@@H](C)CN(C)C(=O)OC(C)(C)C)C2=C(F)C=1C1(NC(=O)OCC=2C=CC=CC=2)CC1 BNFKLLOGMXXMED-IBGZPJMESA-N 0.000 description 1
- 125000006534 ethyl amino methyl group Chemical group [H]N(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 235000019253 formic acid Nutrition 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
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 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
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052740 iodine 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
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 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
- UXJRQNXHCZKHRJ-UHFFFAOYSA-N methyl 2,3,4,5,6-pentafluorobenzoate Chemical compound COC(=O)C1=C(F)C(F)=C(F)C(F)=C1F UXJRQNXHCZKHRJ-UHFFFAOYSA-N 0.000 description 1
- NHMVBKPIIOFQAV-UHFFFAOYSA-N methyl 4-ethenyl-2,3,5,6-tetrafluorobenzoate Chemical compound COC(=O)C1=C(F)C(F)=C(C=C)C(F)=C1F NHMVBKPIIOFQAV-UHFFFAOYSA-N 0.000 description 1
- 125000006533 methyl amino methyl group Chemical group [H]N(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000012046 mixed solvent 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
- 150000002825 nitriles Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229960001699 ofloxacin Drugs 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- CMTPJMNSFKHJBR-FJXQXJEOSA-N pazufloxacin hydrochloride Chemical compound Cl.C([C@@H](N1C2=C(C(C(C(O)=O)=C1)=O)C=C1F)C)OC2=C1C1(N)CC1 CMTPJMNSFKHJBR-FJXQXJEOSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 229950010879 phenamine Drugs 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 239000011698 potassium fluoride Substances 0.000 description 1
- 235000003270 potassium fluoride Nutrition 0.000 description 1
- 239000000843 powder Substances 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
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000006235 propyl amino ethyl group Chemical group [H]N(C([H])([H])C([H])([H])*)C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- BEOOHQFXGBMRKU-UHFFFAOYSA-N sodium cyanoborohydride Chemical compound [Na+].[B-]C#N BEOOHQFXGBMRKU-UHFFFAOYSA-N 0.000 description 1
- 239000011775 sodium fluoride Substances 0.000 description 1
- 235000013024 sodium fluoride Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- WMOVHXAZOJBABW-UHFFFAOYSA-N tert-butyl acetate Chemical compound CC(=O)OC(C)(C)C WMOVHXAZOJBABW-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- BPECCYFUJCNQOR-UHFFFAOYSA-N tert-butyl n-methoxycarbonylcarbamate Chemical compound COC(=O)NC(=O)OC(C)(C)C BPECCYFUJCNQOR-UHFFFAOYSA-N 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000010998 test method Methods 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
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/06—Peri-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/06—Peri-condensed systems
-
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/06—Peri-condensed systems
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Communicable Diseases (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10062888 | 1988-04-23 | ||
| JP1075873A JPH0228178A (ja) | 1988-04-23 | 1989-03-28 | 新規なピリドンカルボン酸誘導体およびその塩並びにそれらの製造法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| SE8901464D0 SE8901464D0 (sv) | 1989-04-21 |
| SE8901464L SE8901464L (sv) | 1989-10-24 |
| SE504625C2 true SE504625C2 (sv) | 1997-03-17 |
Family
ID=26417038
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE8901464A SE504625C2 (sv) | 1988-04-23 | 1989-04-21 | Pyridonkarboxylsyraderivat och salter därav, förfarande för deras framställning samt antibakteriella medel innehållande dessa |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US4990508A (no) |
| JP (1) | JPH0228178A (no) |
| KR (1) | KR910005833B1 (no) |
| AT (1) | AT398422B (no) |
| AU (1) | AU601324B2 (no) |
| BE (1) | BE1003252A4 (no) |
| CA (1) | CA1340493C (no) |
| CH (1) | CH680793A5 (no) |
| DE (1) | DE3913245C2 (no) |
| DK (1) | DK175649B1 (no) |
| ES (1) | ES2016012A6 (no) |
| FI (1) | FI91529C (no) |
| FR (1) | FR2630441B1 (no) |
| GB (1) | GB2217710B (no) |
| HU (2) | HU205759B (no) |
| IL (1) | IL89931A (no) |
| IT (1) | IT1231760B (no) |
| NL (1) | NL192832C (no) |
| NO (1) | NO171214C (no) |
| NZ (1) | NZ228847A (no) |
| SE (1) | SE504625C2 (no) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5104868A (en) * | 1988-06-21 | 1992-04-14 | Pfizer Inc. | Tricyclic derivatives of 7-substituted-6-fluoro-1,4-dihydroquinol-4-one-3-carboxylic acids and esters |
| EP0997466A1 (en) * | 1988-10-24 | 2000-05-03 | PROCTER & GAMBLE PHARMACEUTICALS, INC. | Novel antimicrobial lactam-quinolones |
| EP0449445A3 (en) * | 1990-03-27 | 1993-08-25 | Pfizer Inc. | Preparation of beta-ketoesters useful in preparing quinolone antibiotics |
| IT1248011B (it) * | 1991-06-07 | 1995-01-05 | Mediolanum Farmaceutici Spa | Procedimento per la preparazione dell'acido 9-fluoro-10- (4-metil-1-piperazinil)-7-oxo-2,3-diidro-7h-pirido (1,2,3-de) (1,4)benzotiadin-6-carbossilico cloridrato. |
| EG20543A (en) * | 1992-10-30 | 1999-07-31 | Procter & Gamble | Process for preparing of novel antimicrobial -5- (n-heterosubstituted amino) quinolones |
| TW252107B (no) * | 1993-08-27 | 1995-07-21 | Hokuriku Pharmacetical Co Ltd | |
| IT1270836B (it) * | 1993-10-27 | 1997-05-13 | Archimica Spa | Procedimento per la preparazione di rufloxacina e suoi sali |
| IT1270834B (it) * | 1993-10-27 | 1997-05-13 | Archimica Spa | Disolfuro chinolico |
| USH1480H (en) * | 1993-12-09 | 1995-09-05 | The Procter & Gamble Company | Methods of using dyphylline for the promotion of hair growth |
| JP4694669B2 (ja) | 1999-03-17 | 2011-06-08 | 第一三共株式会社 | 医薬組成物 |
| EP1490372B1 (de) | 2002-03-21 | 2008-01-16 | Basf Aktiengesellschaft | Fungizide triazolopyrimidine, verfahren zu ihrer herstellung und ihre verwendung zur bekämpfung von schadpilzen sowie sie enthaltende mittel |
| CN1332962C (zh) * | 2005-07-12 | 2007-08-22 | 武汉人福药业有限责任公司 | 一种合成甲磺酸帕珠沙星中间体的方法 |
| US8063221B2 (en) * | 2006-03-13 | 2011-11-22 | Kyorin Pharmaceutical Co., Ltd. | Aminoquinolones as GSK-3 inhibitors |
| CA2699151A1 (en) * | 2007-09-11 | 2009-03-19 | Activx Biosciences, Inc. | Cyanoaminoquinolones and tetrazoloaminoquinolones as gsk-3 inhibitors |
| EP2203459B1 (en) | 2007-09-12 | 2016-03-16 | Kyorin Pharmaceutical Co., Ltd. | Spirocyclic aminoquinolones as gsk-3 inhibitors |
| MX2011009414A (es) * | 2009-03-11 | 2011-10-19 | Kyorin Seiyaku Kk | 7-cicloalquiloaminoquinolonas como inhibidores de gsk-3. |
| CN101928290B (zh) * | 2009-11-27 | 2011-11-09 | 浙江司太立制药股份有限公司 | 一种甲磺酸帕珠沙星的纯化方法 |
| CN102295652A (zh) * | 2011-06-27 | 2011-12-28 | 辽宁海神联盛制药有限公司 | 一种甲磺酸帕珠沙星合成工艺的改进方法 |
| CN102850375A (zh) * | 2012-03-06 | 2013-01-02 | 江西师范大学 | 一类多取代吡啶并[4, 3-d]噁嗪化合物及制备方法 |
| CN103772412B (zh) * | 2012-10-23 | 2016-03-16 | 浙江海森药业有限公司 | 一种帕珠沙星中间体的制备方法 |
| CN105622632B (zh) * | 2014-10-29 | 2018-06-29 | 浙江海森药业股份有限公司 | 一种喹诺酮类化合物及其制备方法 |
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| US3883522A (en) * | 1974-02-11 | 1975-05-13 | Riker Laboratories Inc | Substituted pyrido(1,2,3-de)-1,4-benzoxazines |
| DE3211984C2 (de) * | 1981-05-21 | 1986-04-03 | Dieter Dr. 7900 Ulm Benz | Rotierende Zahnbürste |
| JPS591489A (ja) * | 1982-06-29 | 1984-01-06 | Dai Ichi Seiyaku Co Ltd | ピリドベンゾオキサジン誘導体 |
| DE3234529A1 (de) * | 1982-09-17 | 1984-03-22 | Bayer Ag, 5090 Leverkusen | Substituierte benzoxazin-derivate |
| US4603199A (en) * | 1982-10-25 | 1986-07-29 | Riker Laboratories, Inc. | Phenyl-substituted tricyclic antibacterial agent intermediates |
| US4540694A (en) * | 1984-04-26 | 1985-09-10 | Abbott Laboratories | 1-Pyridine substituted quino-benoxazines and antibacterial use |
| US4607032A (en) * | 1984-04-26 | 1986-08-19 | Abbott Laboratories | Quino-benoxazine antibacterial compounds |
| US4822801A (en) * | 1984-07-20 | 1989-04-18 | Warner-Lambert Company | 4-oxo-1,4-dihydroquinoline-3-carboxylic acid derivative as antibacterial agents |
| US4623650A (en) * | 1984-12-06 | 1986-11-18 | Pfizer Inc. | Antibiotic derivatives of 7-phenyl-1,4-dihydro-4-oxo-3-quinolinecarboxylic acids |
| DE3517709A1 (de) * | 1985-01-05 | 1986-07-10 | Bayer Ag | Basische zubereitungen von chinoloncarbonsaeuren |
| DE3525108A1 (de) * | 1985-06-07 | 1986-12-11 | Bayer Ag, 5090 Leverkusen | Antibakteriell wirksame chinoloncarbonsaeureester |
| DE3522405A1 (de) * | 1985-06-22 | 1987-01-02 | Bayer Ag | 1,8-verbrueckte 4-chinolon-3-carbonsaeuren, verfahren zu ihrer herstellung sowie diese enthaltende arzneimittel und ihre verwendung zur herstellung von arzneimitteln |
| DE3522406A1 (de) * | 1985-06-22 | 1987-01-02 | Bayer Ag | Verfahren zur herstellung von 1,8-verbrueckten 4-chinolon-3-carbonsaeuren |
| DE3543513A1 (de) * | 1985-12-10 | 1987-06-11 | Bayer Ag | Enantiomerenreine 1,8-verbrueckte 4-chinolon-3-carbonsaeuren, verfahren zu ihrer herstellung sowie diese enthaltende arzneimittel und ihre verwendung zur herstellung von arzneimitteln |
| DE3601567A1 (de) * | 1986-01-21 | 1987-07-23 | Bayer Ag | 7-(azabicycloalkyl)-chinoloncarbonsaeure- und -naphthyridon-carbonsaeure-derivate |
| US4777253A (en) * | 1986-04-25 | 1988-10-11 | Abbott Laboratories | Process for preparation of racemate and optically active ofloxacin and related derivatives |
| IT1196429B (it) * | 1986-07-01 | 1988-11-16 | Mediolanum Farmaceutici Srl | Processo per la preparazione di pirido benzotiazine ad attivita' antibatterica e loro sali con acidi solfonici |
| DE3623757A1 (de) * | 1986-07-15 | 1988-01-21 | Bayer Ag | Neue 1,8-verbrueckte 4-chinoloncarbonsaeuren und diese enthaltende arzneimittel |
| DE3639465A1 (de) * | 1986-11-18 | 1988-05-19 | Hoechst Ag | Optisch aktive gyrasehemmer, ihre herstellung und verwendung als antibiotika |
| DE3641661A1 (de) * | 1986-12-05 | 1988-06-30 | Bayer Ag | Verfahren zur herstellung von chinoloncarbonsaeureestern |
| DE3711193A1 (de) * | 1987-04-02 | 1988-10-13 | Bayer Ag | 5-substituierte chinolon- und naphthyridoncarbonsaeure-derivate |
| JP2598921B2 (ja) * | 1987-10-05 | 1997-04-09 | 富山化学工業株式会社 | 新規なキノリン誘導体およびその塩 |
| DE3810080A1 (de) * | 1988-03-25 | 1989-10-05 | Bayer Ag | Trisubstituierte 1,3,5-triazin-2,4,6-trione |
| DE3815481A1 (de) * | 1988-05-06 | 1989-11-16 | Sandoz Ag | Sulfonsaeuregruppenfreie basische verbindung |
| US5039682A (en) * | 1988-06-21 | 1991-08-13 | Pfizer Inc. | 6-fluoro-1,4-dihydroquinol-4-one-3-carboxylic acid derivatives and intermediates therefor |
-
1989
- 1989-03-28 JP JP1075873A patent/JPH0228178A/ja active Granted
- 1989-04-11 GB GB8908096A patent/GB2217710B/en not_active Expired - Lifetime
- 1989-04-11 CA CA000596351A patent/CA1340493C/en not_active Expired - Lifetime
- 1989-04-12 IL IL89931A patent/IL89931A/xx unknown
- 1989-04-12 AU AU32661/89A patent/AU601324B2/en not_active Expired
- 1989-04-13 US US07/337,656 patent/US4990508A/en not_active Expired - Lifetime
- 1989-04-20 DK DK198901925A patent/DK175649B1/da not_active IP Right Cessation
- 1989-04-21 NL NL8901007A patent/NL192832C/nl not_active IP Right Cessation
- 1989-04-21 ES ES8901409A patent/ES2016012A6/es not_active Expired - Fee Related
- 1989-04-21 DE DE3913245A patent/DE3913245C2/de not_active Expired - Lifetime
- 1989-04-21 NZ NZ228847A patent/NZ228847A/en unknown
- 1989-04-21 AT AT0095989A patent/AT398422B/de not_active IP Right Cessation
- 1989-04-21 NO NO891650A patent/NO171214C/no not_active IP Right Cessation
- 1989-04-21 HU HU891938A patent/HU205759B/hu unknown
- 1989-04-21 KR KR1019890005253A patent/KR910005833B1/ko not_active IP Right Cessation
- 1989-04-21 CH CH1530/89A patent/CH680793A5/de not_active IP Right Cessation
- 1989-04-21 IT IT8947875A patent/IT1231760B/it active
- 1989-04-21 SE SE8901464A patent/SE504625C2/sv not_active IP Right Cessation
- 1989-04-21 FI FI891910A patent/FI91529C/fi not_active IP Right Cessation
- 1989-04-21 FR FR898905335A patent/FR2630441B1/fr not_active Expired - Lifetime
- 1989-04-24 BE BE8900452A patent/BE1003252A4/fr not_active IP Right Cessation
-
1995
- 1995-06-30 HU HU95P/P00674P patent/HU211568A9/hu unknown
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