KR930016421A - 퀴놀론- 및 나프티리돈-카르복실산 유도체 - Google Patents
퀴놀론- 및 나프티리돈-카르복실산 유도체 Download PDFInfo
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- KR930016421A KR930016421A KR1019930000227A KR930000227A KR930016421A KR 930016421 A KR930016421 A KR 930016421A KR 1019930000227 A KR1019930000227 A KR 1019930000227A KR 930000227 A KR930000227 A KR 930000227A KR 930016421 A KR930016421 A KR 930016421A
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- alkyl
- methyl
- halogen
- carboxylic acid
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- -1 naphthyridone carboxylic acid derivatives Chemical class 0.000 claims abstract 18
- 238000000034 method Methods 0.000 claims abstract 3
- 229910052736 halogen Inorganic materials 0.000 claims 15
- 150000002367 halogens Chemical class 0.000 claims 15
- 229910052739 hydrogen Inorganic materials 0.000 claims 12
- 150000001875 compounds Chemical class 0.000 claims 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 6
- 239000002253 acid Substances 0.000 claims 6
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 6
- 239000001257 hydrogen Substances 0.000 claims 6
- 229910052801 chlorine Inorganic materials 0.000 claims 5
- 239000000460 chlorine Substances 0.000 claims 5
- 150000003839 salts Chemical class 0.000 claims 5
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical class NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims 4
- 229910052783 alkali metal Inorganic materials 0.000 claims 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 4
- 229910052794 bromium Inorganic materials 0.000 claims 4
- 150000001735 carboxylic acids Chemical class 0.000 claims 4
- 150000004677 hydrates Chemical class 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 4
- 150000003378 silver Chemical class 0.000 claims 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 229910052731 fluorine Inorganic materials 0.000 claims 3
- 125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 claims 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 2
- 208000035473 Communicable disease Diseases 0.000 claims 2
- 239000002585 base Substances 0.000 claims 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 230000005764 inhibitory process Effects 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- XOQQVKDBGLYPGH-UHFFFAOYSA-N 2-oxo-1h-quinoline-3-carboxylic acid Chemical compound C1=CC=C2NC(=O)C(C(=O)O)=CC2=C1 XOQQVKDBGLYPGH-UHFFFAOYSA-N 0.000 claims 1
- BEOAQNGVMXFVRN-JOYOIKCWSA-N 7-[(4as,7as)-1,2,3,4,4a,5,7,7a-octahydropyrrolo[3,4-b]pyridin-6-yl]-1-cyclopropyl-5,6,8-trifluoro-4-oxoquinoline-3-carboxylic acid Chemical compound C12=C(F)C(N3C[C@H]4NCCC[C@H]4C3)=C(F)C(F)=C2C(=O)C(C(=O)O)=CN1C1CC1 BEOAQNGVMXFVRN-JOYOIKCWSA-N 0.000 claims 1
- WEXQOLCYKFJAJZ-ZUZCIYMTSA-N 7-[(4as,7as)-1,2,3,4,4a,5,7,7a-octahydropyrrolo[3,4-b]pyridin-6-yl]-1-cyclopropyl-6,8-difluoro-4-oxoquinoline-3-carboxylic acid Chemical compound C12=C(F)C(N3C[C@H]4NCCC[C@H]4C3)=C(F)C=C2C(=O)C(C(=O)O)=CN1C1CC1 WEXQOLCYKFJAJZ-ZUZCIYMTSA-N 0.000 claims 1
- VRXORHRXNRJZCQ-ZUZCIYMTSA-N 7-[(4as,7as)-1,2,3,4,4a,5,7,7a-octahydropyrrolo[3,4-b]pyridin-6-yl]-8-chloro-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid Chemical compound C12=C(Cl)C(N3C[C@H]4NCCC[C@H]4C3)=C(F)C=C2C(=O)C(C(=O)O)=CN1C1CC1 VRXORHRXNRJZCQ-ZUZCIYMTSA-N 0.000 claims 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 239000004599 antimicrobial Substances 0.000 claims 1
- 239000011230 binding agent Substances 0.000 claims 1
- YTIVTFGABIZHHX-UHFFFAOYSA-N butynedioic acid Chemical compound OC(=O)C#CC(O)=O YTIVTFGABIZHHX-UHFFFAOYSA-N 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- 208000015181 infectious disease Diseases 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 239000011630 iodine Substances 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 239000002516 radical scavenger Substances 0.000 claims 1
- 239000003674 animal food additive Substances 0.000 abstract 1
- 230000000844 anti-bacterial effect Effects 0.000 abstract 1
Classifications
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Tropical Medicine & Parasitology (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Fodder In General (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
- Apparatus For Disinfection Or Sterilisation (AREA)
Abstract
Description
Claims (13)
- 하기 일반식(Ⅰ)의 퀴놀론- 및 나프티리돈-카르복실산 유도체, 및 그의 제약상 이용 가능한 수화물 및 산부가염, 및 기초 카르복실산의 알칼리 금속염, 알칼리 토금속염, 은염 및 구아니디늄염.상기 식에서, A는 CH, CF, CCl, C-OCH3, C-CH3또는 N을 나타내고, X1은 H, 할로겐, NH2또는 CH3를 나타내고, R1은 C1-C3-알킬, FCH2CH2-, 시클로프로필 또는 할로겐에 의하여 일치환 내지 삼치환될 수 있는 페닐을 나타내거나, 또는 A 및 R1은 함께 C-O-CH2-CH(CH3)- 구조의 다리를 나타낼 수 있고, R2는 H, 히드록실, 할로겐 또는 아미노에 의하여 치환될 수 있는 C1-C3-알킬을 나타내거나 또는 5-메틸-2-옥소-1,3-디옥솔-4-일-메틸을 나타내고, B는 하기 일반식의 기를 나타내고, 여기에서, Y는 O 또는 CH2를 나타내고, R3은 C2-C5-옥소알킬, CH2-CO-C6H5, CH2CH2CO2R´,, -CH=CH-CO2R´ 또는 CH2CH2-CN을 나타내고, 여기에서, R´은 수소 또는 C1-C3-알킬을 나타내고, R4는 H, C1-C3-알킬, 5-메틸-2-옥소-1,3-디옥솔-4-일-메틸, C2-C5-옥소알킬, CH2-CO-C6H5, CH2CH2CO2R´,, -CH=CH-CO2R´ 또는 CH2CH2-CN을 나타내고, 여기에서, R´은 수소 또는 C1-C3-알킬을 나타낸다.
- 제1항에 있어서, A가 CH, CF, CCl, C-OCH3또는 N을 나타내고, X1은 H, F, Cl, Br, NH2또는 CH3를 나타내고, R1이 C2H5, 시클로프로필 또는 2,4-디플루오로페닐을 나타내거나, 또는 A 및 R1이 함께 C-O-CH2-CH(CH3)- 구조의 다리를 나타낼 수 있고, R2가 H, CH3, C2H5또는 5-메틸-2-옥소-1,3-디옥솔-4-일-메틸을 나타내고, B가 하기 일반식의 기를 나타내고, 여기에서, Y는 O 또는 CH2를 나타내고, R3은 CH2-CO-CH3, CH2-CO-C6H5, CH2CH2-CO-CH3, CH2CH2CO2R´,, -CH=CH-CO2R´ 또는 CH2CH2-CN을 나타내고, 여기에서, R´은 C1-C2-알킬을 나타내고, R4는 H, C1-C3-알킬, 5-메틸-2-옥소-1,3-디옥솔-4-일-메틸, CH2-CO-CH3, CH2-CO-C6H5, CH2CH2-CO-CH3, CH2CH2CO2R´,, -CH=CH-CO2R´ 또는 CH2CH2-CN을 나타내고, 여기에서, R´은 C1-C2-알킬을 나타내는 일반식(Ⅰ)의 퀴놀론- 및 나프티리돈-카르복실산 유도체, 및 제약상 이용 가능한 그의 수화물 및 산부가염, 및 기초 카르복실산의 알칼리 금속염, 알칼리 토금속염, 은염 및 구아니디늄염.
- 제1항에 있어서, A가 CH, CF, CCl, C-OCH3또는 N을 나타내고, X1은 H, F, Cl, Br, NH2또는 CH3를 나타내고, R1은 C2H5, 시클로프로필 또는 2,4-디플루오로페닐을 나타내거나, 또는 A 및 R1은 함께 C-O-CH2-CH(CH3)- 구조의 다리를 나타낼 수 있고, R2는 H, CH3, C2H5또는 5-메틸-2-옥소-1,3-디옥솔-4-일-메틸을 나타내고, B는 하기 일반식의 기를 나타내고, 여기에서, Y는 O 또는 CH2를 나타내고, R4는 CH2-CO-CH3, CH2-CO-C6H5, CH2CH2-CO-CH3, CH2CH2CO2R´,, -CH=CH-CO2R´ 또는 CH2CH2-CN을 나타내고, 여기에서, R´은 C1-C2-알킬을 나타내는 일반식(Ⅰ)의 퀴놀론- 및 나프티리돈-카르복실산 유도체, 및 제약상 이용가능한 그의 수화물 및 산부가염, 및 기초 카르복실산의 알칼리 금속염, 알칼리 토금속염, 은염 및 구아니디늄염.
- 8-클로로-1-시클로프로필-7-([S,S]-2,8-디아자비시클로-[4,3,0]논-8-일)-6-플루오로-1, 4-디히드로-4-옥소-3-퀴놀린카르복실산, 및 제약상 허용되는 그의 수화물 및 산부가염, 및 기초 카르복실산의 알칼리 금속염, 알칼리 토금속염, 은염 및 구아니디늄염.
- 1-시클로프로필-7-([S,S]-2,8-디아자비시클로[4,3,0]논-8-일)-6,8-디플루오로-1, 4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-시클로프로필-7-([S,S]-2,8-디아자비시클로-[4,3,0]논-8-일)-6-플루오로-1, 4-디히드로-4-옥소-3-퀴놀린카르복실산 및 1-시클로프로필-7-([S,S]-2,8-디아자비시클로[4,3,0]논-8-일)-5,6,8-트리플루오로-1, 4-디히드로-4-옥소-3-퀴놀린카르복실산으로 이루어진 군 중에서 선택된 퀴놀론카르복실산 및 그의 염.
- 하기 일반식(Ⅱ)의 화합물을, 바람직하게는 산 결합제의 존재 하에 일반식(Ⅲ)의 화합물과 반응시키는 것을 특징으로 하는 제1 내지 3항 중 어느 한 항에 따른 하기 일반식(Ⅰ)의 퀴놀론- 및 나프티리돈-카르복실산 유도체의 제조 방법.상기 식들에서, A가 CH, CF, CCl, C-OCH3, C-CH3또는 N을 나타내고, X1은 H, 할로겐, NH2또는 CH3를 나타내고, R1은 C1-C3-알킬, FCH2CH2-, 시클로프로필 또는 할로겐에 의하여 일치환 내지 삼치환될 수 있는 페닐을 나타내거나, 또는 A 및 R1이 함께 C-O-CH2-CH(CH3)- 구조의 다리를 나타낼 수 있고, R2는 H, 히드록실, 할로겐 또는 아미노에 의하여 치환될 수 있는 C1-C3-알킬을 나타내거나 또는 5-메틸-2-옥소-1,3-디옥솔-4-일-메틸을 나타내고, B는 하기 일반식의 기를 나타내고, 여기에서, Y는 O 또는 CH2를 나타내고, R3는 C2-C5-옥소알킬, CH2-CO-C6H5,CH2CH2-CO2R´ 또는 CH2CH2-CN을 나타내고, 여기에서 R´은 수소 또는 C1-C3-알킬을 나타내고, X3은 할로겐, 특히 염소, 브롬 또는 요오드를 나타낸다.
- 하기 일반식(Ⅱ)의 화합물을 디알킬 아세틸렌디카르복실레이트, 알킬 프로피올레이트 또는 하기 일반식(Ⅳ)의 화합물과 같은 미하엘(Michael) 수용체와 반응시키는 것을 특징으로 하는 제1 내지 제3항 중 어느 한 항에 따른 하기 일반식(Ⅰ)의 퀴놀론- 및 나프티리돈-카르복실산 유도체의 제조방법.상기 식들에서, A는 CH, CF, CCl, C-OCH3, C-CH3또는 N을 나타내고, X1은 H, 할로겐, NH2또는 CH3를 나타내고, R1은 C1-C3-알킬, FCH2CH2-, 시클로프로필 또는 할로겐에 의하여 일치환 내지 삼치환될 수 있는 페닐을 나타내거나, 또는 A 및 R1이 함께 C-O-CH2-CH(CH3)- 구조의 다리를 나타낼 수 있고, R2는 H, 히드록실, 할로겐 또는 아미노에 의하여 치환될 수 있는 C1-C3-알킬을 나타내거나 또는 5-메틸-2-옥소-1,3-디옥솔-4-일-메틸을 나타내고, B는 다음 일반식의 기를 나타내고, 여기에서, Y는 O 또는 CH2를 나타내고, R3는 CH2CH2-CO-CH3, CH2CH2-CO2R´,, -CH=CH-CO2R´또는 CH2CH2-CN을 나타내고, 여기에서, R´은 수소 또는 C1-C3-알킬을 나타내고, R5는 COCH3, CO2R´ 또는 CN을 나타낸다.
- 하기 일반식(Ⅴ)의 화합물을, 적합하다면 산 포집제의 존재 하에 하기 일반식(Ⅳ)의 화합물의 순수한 에난티오머와 반응시키고, 반응 생성물을 임의로 하기 일반식(Ⅲa)의 화합물, 또는 디알킬 아세틸렌디카르복실레이트, 알킬 프로피올레이트 또는 하기 일반식(Ⅳ)의 화합물과 같은 미하엘 수용체와 추가로 반응시키는 것을 특징으로 하는 제1 내지 제3항 중 어느 한 항에 따른 하기 일반식(Ⅰ)의 퀴놀론- 및 나프티리돈-카르복실산 유도체의 제조방법.상기 식들에서, A는 CH, CF, CCl, C-OCH3, C-CH3또는 N을 나타내고, X1은 H, 할로겐, NH2또는 CH3를 나타내고, R1은 C1-C3-알킬, FCH2CH2-, 시클로프로필 또는 할로겐에 의하여 일치환 내지 삼치환될 수 있는 페닐을 나타내거나, 또는 A 및 R1은 함께 C-O-CH2-CH(CH3)- 구조의 다리를 나타낼 수 있고, R2는 H, 히드록실, 할로겐 또는 아미노에 의하여 치환될 수 있는 C1-C3-알킬을 나타내거나 또는 5-메틸-2-옥소-1,3-디옥솔-4-일-메틸을 나타내고, B는 하기 일반식의 기를 나타내고, 여기에서 Y는 O 또는 CH2를 나타내고, R4는 H, C1-C3-알킬, C2-C5-옥소알킬, CH2CO-C6H5, CH2CH|2-CO2R´, R´O2C-CH=C-CO2R´, -CH=CH-CO2R´또는 CH2CH2-CN을 나타내거나 또는 5-메틸-2-옥소-1,3-디옥솔-4-일-메틸을 나타내고, 여기에서, R´은 수소 또는 C1-C3-알킬을 나타내고, X2는 할로겐, 특히 불소 또는 염소를 나타내고, Y는 0 또는 CH2를 나타내고, R4´는 H 또는 C1-C3-알킬을 나타내고, X3는 할로겐, 특히 염소, 브롬 또는 요오드를 나타내고, R4˝는 C2-C5-옥소알킬, CH2-CO-C6H5, CH2CH2CO2R´또는 CH2CH2-CN을 나타내고, 여기에서, R´은 수소 또는 C1-C3-알킬이며, R5는 COCH3, CO2R´또는 CN을 나타낸다.
- 질병의 억제를 위한 제1 내지 5항 중 어느 한 항에 따른 퀴놀론- 및 나프티리돈-카르복실산 유도체.
- 감염성 질환의 억제를 위한 제1 내지 5항 중 어느 한 항에 따른 퀴놀론- 및 나프티리돈-카르복실산 유도체.
- 제1 내지 5항 중 어느 한 항에 따른 퀴놀론- 및 나프티리돈-카르복실산 유도체를 함유하는 의약.
- 제1 내지 5항 중 어느 한 항에 따른 퀴놀론- 및 나프티리돈-카르복실산 유도체를 함유하는 항균제.
- 감염 질환의 억제용 의약의 제조를 위한 제1 내지 5항 중 어느 한 항에 따른 퀴놀론- 및 나프티리돈-카르복실산 유도체의 용도.※ 참고사항 : 최초출원 내용에 의하여 공개되는 것임.
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DE4208792A DE4208792A1 (de) | 1992-03-19 | 1992-03-19 | Enantiomerenreine chinolincarbonsaeure-derivate |
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UA106556C2 (uk) * | 2013-05-13 | 2014-09-10 | Наталья Николаевна Деркач | СПОСІБ ОДЕРЖАННЯ (1-ЦИКЛОПРОПІЛ-6-ФТОР-1,4-ДИГІДРО-8-МЕТОКСІ-7-[(4aS,7aS)-ОКТАГІДРО-6Н-ПІРОЛО[3,4-b]-4-ОКСО-3-ХІНОЛІНКАРБОНОВОЇ КИСЛОТИ |
CN103724262B (zh) * | 2013-12-10 | 2016-05-18 | 广东省第二人民医院 | 一种氟喹诺酮银化合物及其制备方法和用途 |
CN104860944A (zh) * | 2015-06-09 | 2015-08-26 | 内蒙古东北六药集团有限公司 | 盐酸莫西沙星的生产方法 |
CN108872413B (zh) * | 2018-04-27 | 2021-06-08 | 山东齐都药业有限公司 | 检测(s,s)-2,8-二氮杂双环[4,3,0]壬烷中对映异构体含量的方法 |
CN110627768B (zh) * | 2018-06-22 | 2021-11-09 | 扬子江药业集团有限公司 | 一种莫西沙星降解杂质j的制备方法 |
CN110183445B (zh) * | 2019-06-28 | 2021-08-24 | 昆明学院 | 莫西沙星及其衍生物的合成方法 |
RU2713932C1 (ru) * | 2019-10-31 | 2020-02-11 | федеральное государственное автономное образовательное учреждение высшего образования "Казанский (Приволжский) федеральный университет" (ФГАОУ ВО КФУ) | Соединения фторхинолонового ряда на основе производных пиридоксина, обладающие антибактериальными свойствами |
CN112939849B (zh) * | 2019-12-11 | 2022-05-03 | 浙江新和成股份有限公司 | 一种(s,s)-2,8-二氮杂双环[4.3.0]壬烷中间体及其制备方法和应用 |
CN110981874A (zh) * | 2020-03-05 | 2020-04-10 | 北京四环生物制药有限公司 | 一种盐酸莫西沙星的制备方法 |
CN112409352B (zh) * | 2020-11-20 | 2022-05-24 | 华南理工大学 | 一类莫西沙星类药物衍生物及其制备方法和应用 |
CN112574197B (zh) * | 2020-12-07 | 2021-12-31 | 泰安汉威集团有限公司 | 一种化合物c的手性纯化方法 |
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JPH0754229B2 (ja) * | 1987-09-28 | 1995-06-07 | 松下冷機株式会社 | 冷蔵庫 |
DE3906365A1 (de) * | 1988-07-15 | 1990-01-18 | Bayer Ag | 7-(1-pyrrolidinyl)-3-chinolon- und -naphthyridoncarbonsaeure-derivate, verfahren sowie substituierte (oxa)diazabicyclooctane und -nonane als zwischenprodukte zu ihrer herstellung, und sie enthaltende antibakterielle mittel und futterzusatzstoffe |
AU5123690A (en) * | 1989-03-13 | 1990-09-13 | Bristol-Myers Squibb Company | 5-substituted-1,4-dihydro-4-oxo-nephthyridine-3-carboxylate antibacterial agents |
DE3910663A1 (de) * | 1989-04-03 | 1990-10-04 | Bayer Ag | 5-alkylchinoloncarbonsaeuren |
JPH03188080A (ja) * | 1989-12-15 | 1991-08-16 | Banyu Pharmaceut Co Ltd | ピリドンカルボン酸誘導体 |
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