KR890009911A - 7-(1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린 카르복실산의 유도체, 그의 제조방법 및 제약학적 조성물 - Google Patents
7-(1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린 카르복실산의 유도체, 그의 제조방법 및 제약학적 조성물 Download PDFInfo
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- KR890009911A KR890009911A KR1019880017747A KR880017747A KR890009911A KR 890009911 A KR890009911 A KR 890009911A KR 1019880017747 A KR1019880017747 A KR 1019880017747A KR 880017747 A KR880017747 A KR 880017747A KR 890009911 A KR890009911 A KR 890009911A
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- azetidinyl
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- difluoro
- cyclopropyl
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- 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
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- C07D455/03—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing quinolizine ring systems directly condensed with at least one six-membered carbocyclic ring, e.g. protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine
- C07D455/04—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing quinolizine ring systems directly condensed with at least one six-membered carbocyclic ring, e.g. protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing a quinolizine ring system condensed with only one six-membered carbocyclic ring, e.g. julolidine
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Abstract
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Description
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Claims (9)
- 하기 일반식(Ⅰ)의 신규한 헤테로 로리형 화합물 :상기식에서, R1은 저급알케닐 또는 알킬라디칼, 할로알킬 라디칼, 시클로알킬 라디칼, 아미노알킬 라디칼, 아릴 아디칼 또는 치환된 아릴라디칼, 특히 1개 이상의 불소원자 치환체를 갖는 라디칼을 나타내고 : R2는 수소원자, 할로겐원자를 나타내거나, R1과 R2가 함께 X기를 형성할 수도 있으며 : R3는 수소원자 또는 저급알킬 라디칼을 나타내고 : R4와 R5와 R6는 독립적으로 수소원자, 저급알킬 라디칼, 히드록시 라디탈, 아미노 라디칼, 아미노알킬 라디칼, 알킬아미노 라디칼, 디알킬아미노 라디칼, 알킬아미노알킬 라디칼, 알콕시 라디칼, 메실옥시라디칼, 히드록시알킬 라디칼, 시아노 라디칼, 아실아미노알킬 라디칼, 카르복실 라디칼, 카르복스 아미도 라디칼, 카르복시알킬 라디칼, 할로겐 원자, 알킬카르복시 라디칼, 예컨대 아세톡시, 아세트아미도 라디칼 또는 아세트아미도알킬 라디칼(이들 마지박 두 라디칼에 있어서, 말단 자유 알킬기는 불소화될 수 있고, 아세트아미도알킬 라디칼내의 질소원자는 알킬치환체를 가질 수 있다)을 나타내고 ; X는 -CH2-CH2-R7은 수소원자, 또는 저급알킬 라디칼을 나타내고 ; R8은 수소원자, 또는 할로겐원자를 나타내며 ; Y는 CH 또는 N을 나타내고 ; 단, R1및 R2가 함께 -O-CH2-CH(CH3)-로 표시되는 연결기를 형성하고, R3,R4및 R6가 수소원자를 나타내고, R5가 히드록시라디칼(OH) 또는 히드록시메틸 라디칼(CH2OH)을 나타내는 일반식(Ⅰ)의 화합물과, R1이 에틸라디칼을 나타내고, R2가 불소원자를 나타내고, R3,R4및 R6가 수소원자를 나타내며 R5가 에틸아미노메틸 라디칼(CH3CH2NHCH2)을 나타내는 일반식(Ⅰ)의 화합물은 제외된다.
- 제1항에 있어서, R6및 R3가 수소원자를 나타내고 R1,R2,R4및 R5가 앞서 정의한 바와 같은 의미를 갖는 일반식(Ⅰ)의 상응함을 특징으로 하는 헤테로고리형 화합물.
- 제1항 또는 제2항에 있어서, R2,R4및 R5가 앞서 정의한 바와같은 의미를 갖는 하기 일반식(Ia)에 상응함을 특징으로 하는 헤테로고리형 화합물 :
- 제1항 또는 제2항에 있어서, 1-(4-플루오로페닐)-6.8-디플루오로-7-(3-메틸-3-트리플루오로아세트아미도-1-아제티디닐)-1,4-디히드로-4-옥소-3-3-퀴놀린카르복실산, 1-(4-플루오로페닐)-6, 8-디플루오로-7-(3-아미노-3-메틸-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-(에틸-6,8-디플루오로-1,4-디히드로-4-옥소-7-(3-메틸-3-트리플루오로아세트아미도-1-아제티디닐)-3-퀴놀린카르복실산, 1-에틸-6,8-디플루오로-7-(3-아미노-3-메틸-1-아제티디닐)-1, 4-디히드로-4-옥소-3-퀴놀린카르복실산, [S]-(-)-9-플루오로-3-메틸-7-옥소-2,3-디히드로-7H-피리도[1,2,3,-데][1,4]벤즈옥사진-10-(3-아미노-3-메틸-1-아제티디닐)-6-카르복실산, [R]-(+)-9-플루오로-3-메틸-7-옥소-2,3-디히드로-7H-피리도[1,2,3-데][1,4]벤즈옥사진-10-(3-아미노-3-메틸-1-아제티디닐)-6 카르복실산, 1-에틸-6-플루오로-7-(3-아미노-3-메틸-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-(2-플루오로메틸)-6-플루오로-7-(3-메틸-3-아미노-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-(2,4-디플루오로페닐)-6-플루오로-7-(3-메틸-3-아미노-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-(2-플루오로에틸)-6,8-디플루오로-7-(3-아미노-3-메틸-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-(4-플루오로페닐)-6-플루오로-7-(3-아미노-3-메틸-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-(2,4-디플루오로페닐)-6,8-디플루오로-7-(3-메틸-3-트리플루오로아세트아미도-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복시산, 1-(2,4-디플루오로페닐)-6,8-디플루오로-7-(3-아미노-3-메틸-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복시산으로 부터 선택된 일반식(Ⅰ)의 화합물.
- 제1항, 제2항 또는 제3항에 있어서, 에틸 1-시클로프로필-6,8-디플루오로-7-(3-히드록시-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실레이트, 1-시클로프로필-6,8-디플루오로-7-(3-히드록시-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 에틸 1-시클로프로필-6,8-디플루오로-7-(3-메실옥시-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실레이트, 에틸 7-(3-아세틸아미노메틸-1-아제티디닐)-1-시클로프로필-6,8-디플루오로-1,4-디히드로-4-옥소-3-퀴놀린카르복실레이트, 1-시클로프로필-6,8-디플루오로-7-(3-카르복시-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-시클로프로필-6,8-디플루오로-7-(3-사이노-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-시클로프로필-6,8-디플루오로-7-(3-사이노-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-시클로프로필-6,8-디플루오로-7-(3-메틸-3-히드록시-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 7-(3-트리플루오로아세트아미도메틸-1-아제티디닐)-1-시클로프로필-6,8-디플루오로-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 7-(3-아미노메틸-1-아제티디닐)-1-시클로프로필-6,8-디플루오로-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-시클로프로필-6,8-디플루오로-7-(3-메실옥시-1-아제티디닐]-6,8-디플루오로-1,4-디히드로-1-시클로프로필-4-옥소-3-퀴놀린카르복실산, 7-(3-N'-에틸아미노메틸-1-아제티디닐)-6,8-디플루오로-1,4-디히드로-1-시클로프로필-4-옥소-3-퀴놀린카르복실산, 1-시클로프로필-6,8-디플루오로-1,4-디히드로-7-(1-1-아제티디닐)-4-옥소-3-퀴놀린카르복실산, 1-시클로프로필-6,8-디플루오로-7(3-메틸-3-트리플루오로아세트아미도-1-아제티디닐)-4-옥소-3-퀴놀린카르복실산, 1-시클로프로필-6,8-디플루오로-1,4-디히드로-7-(3-메틸-3-아메노-1-아제티디닐)-4-옥소-3-퀴놀린카르복실산, 1-시클로프로필-6,8-디플루오로-7-(아세톡시-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-시클로프로필-6-플루오로-7-(3-히드록시-1-아제티디닐(-1,4-디히드로-4-옥소-3-퀴놀린카르복실실산, 1-시클로프로필-6,8-디플루오로-7-(3-아미노-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-시클로프로필-6,8-디플루오로-7(3-트리플루오로아세트아미도메틸-3-메틸-3-메틸-1-아제티디닐(-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-시클로프로필-6,8-디플루오로-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-시클로프로필-6-플루오로-7-(3-트리플루오로아세트아미도에틸아미노메틸-3-메틸-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-시클로프로필-6-플루오로-1,4-디히드로-4-옥소-7-(3-아메노메틸-3-메틸-1-아제티디닐)-3-퀴놀린카르복실산, 1-시클로프로필-6-플루오로-7-(3-에틸아미노메틸-3-메틸-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-시클로프로필-6,8-디플루오로-1,4-디히드로-4-옥소-7-(3-메틸-3-N,N-디메틸아미노-1-아제티디닐)-3-퀴놀린카르복실산, 1-시클로프로필-6-플루오로-7-(3-아미노-3-메틸-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-시클로프로필-6,8-디플루오로-7-(3-디메틸아미노-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-시클로프로필-6-플루오로-7-(3-디메틸아미노-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-시클로프로필-6,8-디플루오로-7-(3-아미노-3-메틸-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 히드로클로라이드, 1-시클로프로필-6,8-디플루오로-7-(3-메틸ㅇ미노-1-아제티디닐-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 1-시클로프로필-6-플루오로-7-(3-아미노-1-아제티디닐)-1,4-디히드로-4-옥소-3-퀴놀린카르복실산, 으로부터 선택되는 일반식(Ⅰ)의 화합물.
- 하기 일반식(Ⅱ)의 헤테로고리형 화합물을 하기 일반식(Ⅲ)의 화합물과 반응시킴을 특징으로 하는, 제1항 내지 제5항중 어느 한항에 따른 일반식(Ⅰ)의 유도체의 제조방법.상기식에서 R1,R2및 R3는 앞서 정의한 바와같은 의미를 가지며, Z은 할로겐원자를 나타낸다.상기식에서, R4,R5및 R6는 앞서 정의한 바와같은 의미를 갖는다.
- 하기 일반식(Ⅱ)의 헤테로고리형 화합물을 하기 일반식(Ⅳ)의 화합물과 반응시킴을 특징으로 하는 제1항 내지 제5항중 어느 한항에 따른 일반식(Ⅰ)의 유도체인 제조방법 :상기식에서 R1,R2및 R3는 앞서 정의한 바와같은 의미를 가지며, Z은 아미노라디칼을 나타낸다.상기식에서, R4,R5및 R6는 앞서 정의한 바와같은 의미를 가지며, A는 할로겐원자, 히드록실 라디칼, 저급 알킬설포닐옥시라디칼 또는 아릴설포닐옥시 라디칼을 나타낸다.
- 특히 항균제로서 사용되기 위한, 제1항 내지 제5항중 어느 한항에 따른 일반식(Ⅰ)의 화합물 또는 치료학상 허용가능한 그의 염.
- 허용가능한 제약학적 보조물외에 제1항 내지 제5항중 어느 한항에 따른 한가지 이상의 일반식(Ⅰ)의 화합물 또는 생리학상 허용가능한 그의 염을 함유하는 것을 특징으로 하는 제약학적 조성물.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
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FR8718289A FR2625200A1 (en) | 1987-12-29 | 1987-12-29 | 7-(1-Azetidinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid derivatives, their preparation and their application as medicaments |
FR8718289 | 1988-07-20 | ||
FR888809816A FR2634483B2 (fr) | 1987-12-29 | 1988-07-20 | Derives des acides 7-(1-azetidinyl)-1,4-dihydro-4-oxoquinoleine-3-carboxyliques, leur preparation et leur application en tant que medicaments |
FR8809816 | 1988-07-20 |
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KR920004136B1 KR920004136B1 (ko) | 1992-05-25 |
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KR (1) | KR920004136B1 (ko) |
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DK (1) | DK726188A (ko) |
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FR (1) | FR2634483B2 (ko) |
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Families Citing this family (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4839355A (en) * | 1987-09-09 | 1989-06-13 | Sterling Drug Inc. | Tricyclic-pyridinylquinoline compounds, their preparation and use |
US5173484A (en) * | 1988-02-05 | 1992-12-22 | Bayer Aktiengesellschaft | Quinolone- and naphthyridone carboxylic acid derivatives, process for their production, antibacterial compositions and feed additives containing them |
DE3814517A1 (de) * | 1988-02-05 | 1989-08-17 | Bayer Ag | Chinolon- und naphthyridoncarbonsaeurederivate, verfahren zu ihrer herstellung und sie enthaltende antibakterielle mittel und futterzusatzstoffe |
JPH0674261B2 (ja) * | 1988-06-21 | 1994-09-21 | 塩野義製薬株式会社 | キノロンカルボン酸誘導体 |
EP0997466A1 (en) * | 1988-10-24 | 2000-05-03 | PROCTER & GAMBLE PHARMACEUTICALS, INC. | Novel antimicrobial lactam-quinolones |
FR2654728B2 (fr) * | 1989-03-16 | 1994-09-23 | Esteve Labor Dr | Derives d'acides pyridone carboxyliques azetidinyl substitues, leur preparation et leur application en tant que medicament. |
FR2644455B1 (fr) * | 1989-03-16 | 1994-09-23 | Esteve Labor Dr | Derives d'acides pyridone carboxyliques azetidinyl substitues, leur preparation et leur application en tant que medicaments |
FR2649106A2 (fr) * | 1989-06-29 | 1991-01-04 | Esteve Labor Dr | Derives d'acides pyridone carboxyliques azetidinyl substitues, leur preparation et leur application en tant que medicament |
NO177302C (no) * | 1989-03-16 | 1995-08-23 | Esteve Labor Dr | Analogifremgangsmåte til fremstilling av terapeutisk aktive substituerte azetidinylkinolon(naftyridon)karboksylsyrederivater |
IE912902A1 (en) * | 1990-08-24 | 1992-02-26 | Abbott Lab | Quinbenzoxazine, quinobenzothiazine, and pyrido-acridine¹antineoplastic agents |
FR2676445B1 (fr) * | 1991-05-16 | 1995-02-03 | Esteve Labor Dr | Derives de pyridone amino acide azetidinyl substitues, leur preparation et leur application en tant que medicaments. |
US5556861A (en) * | 1991-10-01 | 1996-09-17 | Laboratoire Roger Bellon | 1,8 benzonaphthyridine derivatives and antimicrobial compositions |
FR2690161B1 (fr) * | 1992-04-16 | 1995-06-30 | Esteve Labor Dr | Derives de pyridone azetidinyl substitues avec activite antimicrobienne. |
FR2692577B1 (fr) * | 1992-05-26 | 1996-02-02 | Bouchara Sa | Nouvelles quinolones fluorees, leur procede de preparation et les compositions pharmaceutiques en renfermant. |
JP2005097116A (ja) * | 1999-11-11 | 2005-04-14 | Wakunaga Pharmaceut Co Ltd | キノリンカルボン酸誘導体アルカリ金属塩及びこれを用いたキノリンカルボン酸誘導体の精製法 |
WO2005026146A1 (en) * | 2003-09-12 | 2005-03-24 | Warner-Lambert Company Llc | Azetidinyl quinolones as antibacterial agents |
ATE484509T1 (de) * | 2004-08-02 | 2010-10-15 | Glaxo Group Ltd | Antibakterielle mittel |
ES2583146T3 (es) | 2011-12-01 | 2016-09-19 | Purdue Pharma L.P. | Compuestos de piperidina de tipo quinoxalina sustituidos con azetidina y usos de éstos |
KR20150070348A (ko) | 2012-10-16 | 2015-06-24 | 얀센 파마슈티카 엔.브이. | RoRγt의 헤테로아릴 결합 퀴놀리닐 조절제 |
WO2014062667A1 (en) | 2012-10-16 | 2014-04-24 | Janssen Pharmaceutica Nv | Phenyl linked quinolinyl modulators of ror-gamma-t |
PE20150778A1 (es) | 2012-10-16 | 2015-05-23 | Janssen Pharmaceutica Nv | Moduladores de quinolinilo unidos a metileno de ror-gamma-t |
US9328095B2 (en) | 2013-10-15 | 2016-05-03 | Janssen Pharmaceutica Nv | Heteroaryl linked quinolinyl modulators of RORgammat |
US10555941B2 (en) | 2013-10-15 | 2020-02-11 | Janssen Pharmaceutica Nv | Alkyl linked quinolinyl modulators of RORγt |
US9284308B2 (en) | 2013-10-15 | 2016-03-15 | Janssen Pharmaceutica Nv | Methylene linked quinolinyl modulators of RORγt |
US9403816B2 (en) | 2013-10-15 | 2016-08-02 | Janssen Pharmaceutica Nv | Phenyl linked quinolinyl modulators of RORγt |
US9221804B2 (en) | 2013-10-15 | 2015-12-29 | Janssen Pharmaceutica Nv | Secondary alcohol quinolinyl modulators of RORγt |
AU2014334619A1 (en) * | 2013-10-15 | 2016-04-21 | Janssen Pharmaceutica Nv | Alkyl linked quinolinyl modulators of RORyt |
ES2742843T3 (es) * | 2013-10-15 | 2020-02-17 | Janssen Pharmaceutica Nv | Moduladores de quinolinilo de ROR(gamma)t |
CN113045539B (zh) * | 2021-03-30 | 2021-12-07 | 苏州大学 | 2-(4,4-二氯-1-(8-喹啉基)-2-氮杂环丁基)羧酸酯衍生物的制备方法 |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5746986A (en) * | 1980-09-02 | 1982-03-17 | Dai Ichi Seiyaku Co Ltd | Pyrido(1,2,3-de)(1,4)benzoxazine derivative |
US4540690A (en) * | 1982-02-09 | 1985-09-10 | The Upjohn Company | 2-(Phenylmethylene)cycloalkylamines and -azetidines |
US4777175A (en) * | 1982-09-09 | 1988-10-11 | Warner-Lambert Company | Antibacterial agents |
IE55898B1 (en) * | 1982-09-09 | 1991-02-14 | Warner Lambert Co | Antibacterial agents |
US4665079A (en) * | 1984-02-17 | 1987-05-12 | Warner-Lambert Company | Antibacterial agents |
JPS6089480A (ja) * | 1983-10-21 | 1985-05-20 | Dainippon Pharmaceut Co Ltd | ピリドンカルボン酸誘導体 |
JPS60126284A (ja) * | 1983-12-09 | 1985-07-05 | Dainippon Pharmaceut Co Ltd | ピリドンカルボン酸誘導体およびその塩 |
CA1267413A (en) * | 1984-04-26 | 1990-04-03 | Abbott Laboratories | Quino-benoxazine antibacterial compounds |
US4588263A (en) * | 1984-05-02 | 1986-05-13 | International Business Machines Corporation | An adjustable-optical prism with integral-polarizing beam splitter and applications thereof |
JPS61137885A (ja) * | 1984-12-08 | 1986-06-25 | Dainippon Pharmaceut Co Ltd | 1,8−ナフチリジン誘導体、そのエステルおよびその塩 |
US4617308A (en) * | 1985-01-25 | 1986-10-14 | Warner-Lambert Company | 7-substituted amino-1-aryl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acids and derivatives thereof as antibacterial agents |
CN1019114B (zh) * | 1986-03-31 | 1992-11-18 | 三共株式会社 | 喹啉-3-羟酸衍生物的制备方法 |
WO1989003828A1 (en) * | 1987-10-26 | 1989-05-05 | Pfizer Inc. | Azetidinyl quinolone carboxylic acids and esters |
AU603936B2 (en) * | 1988-02-04 | 1990-11-29 | Chenault D. Lee | Disposable vaginal speculum |
-
1988
- 1988-07-20 FR FR888809816A patent/FR2634483B2/fr not_active Expired - Lifetime
- 1988-12-27 US US07/290,315 patent/US4927926A/en not_active Expired - Fee Related
- 1988-12-28 PT PT89352A patent/PT89352B/pt not_active IP Right Cessation
- 1988-12-28 NO NO885797A patent/NO176605C/no unknown
- 1988-12-28 YU YU237088A patent/YU47124B/sh unknown
- 1988-12-28 EP EP88403352A patent/EP0324298B1/fr not_active Expired - Lifetime
- 1988-12-28 DK DK726188A patent/DK726188A/da not_active Application Discontinuation
- 1988-12-28 DE DE8888403352T patent/DE3876969T2/de not_active Expired - Fee Related
- 1988-12-28 ES ES8900318A patent/ES2010114A6/es not_active Expired
- 1988-12-28 JP JP63335712A patent/JPH0813811B2/ja not_active Expired - Lifetime
- 1988-12-29 AU AU27578/88A patent/AU617735B2/en not_active Ceased
- 1988-12-29 KR KR1019880017747A patent/KR920004136B1/ko not_active IP Right Cessation
- 1988-12-29 HU HU886648A patent/HU206206B/hu not_active IP Right Cessation
-
1992
- 1992-12-24 GR GR920403018T patent/GR3006664T3/el unknown
Also Published As
Publication number | Publication date |
---|---|
NO176605B (no) | 1995-01-23 |
HU206206B (en) | 1992-09-28 |
NO176605C (no) | 1995-05-03 |
FR2634483B2 (fr) | 1994-03-04 |
EP0324298A1 (fr) | 1989-07-19 |
PT89352B (pt) | 1993-09-30 |
NO885797L (no) | 1989-06-30 |
DK726188A (da) | 1989-06-30 |
YU237088A (en) | 1990-12-31 |
NO885797D0 (no) | 1988-12-28 |
DE3876969T2 (de) | 1993-05-19 |
HUT50467A (en) | 1990-02-28 |
ES2010114A6 (es) | 1989-10-16 |
US4927926A (en) | 1990-05-22 |
YU47124B (sh) | 1994-12-28 |
KR920004136B1 (ko) | 1992-05-25 |
JPH01301677A (ja) | 1989-12-05 |
DE3876969D1 (de) | 1993-02-04 |
FR2634483A2 (fr) | 1990-01-26 |
AU2757888A (en) | 1989-06-29 |
GR3006664T3 (ko) | 1993-06-30 |
EP0324298B1 (fr) | 1992-12-23 |
AU617735B2 (en) | 1991-12-05 |
JPH0813811B2 (ja) | 1996-02-14 |
DK726188D0 (da) | 1988-12-28 |
PT89352A (pt) | 1989-12-29 |
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