ES8700256A1 - Un derivado de 1,4-dihidro-4-oxonaftiridina - Google Patents

Un derivado de 1,4-dihidro-4-oxonaftiridina

Info

Publication number
ES8700256A1
ES8700256A1 ES542584A ES542584A ES8700256A1 ES 8700256 A1 ES8700256 A1 ES 8700256A1 ES 542584 A ES542584 A ES 542584A ES 542584 A ES542584 A ES 542584A ES 8700256 A1 ES8700256 A1 ES 8700256A1
Authority
ES
Spain
Prior art keywords
unsubstituted
naphthyridines
group
salts
compounds
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
ES542584A
Other languages
English (en)
Other versions
ES542584A0 (es
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Toyama Chemical Co Ltd
Original Assignee
Toyama Chemical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=13845280&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ES8700256(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Toyama Chemical Co Ltd filed Critical Toyama Chemical Co Ltd
Publication of ES542584A0 publication Critical patent/ES542584A0/es
Publication of ES8700256A1 publication Critical patent/ES8700256A1/es
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/61Halogen atoms or nitro radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72Nitrogen atoms
    • C07D213/74Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design 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)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Hydrogenated Pyridines (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

PROCEDIMIENTO PARA LA PREPARACION DE UN DERIVADO DE 1,4-DIHIDRO-4-OXANAFTIRIDINA Y SUS SALES DE FORMULA GENERAL (I) DONDE R2 REPRESENTA UN GRUPO 2-PIPERAZINILO O 3-AMINO-1-PIRROLIDINILO. CONSISTE EN HACER REACCIONAR A UNA TEMPERATURA COMPRENDIDA ENTRE 0J Y 150JC, UN COMPUESTO DE FORMULA GENERAL (II) O UNA SAL DEL MISMO EN EL QUE R1 ES H O UN GRUPO PROTECTOR DEL CARBOXILO Y R3 ES UN HALOGENO CON UN COMPUESTO DE FORMULA R2A-H EN EL QUE R2A ES EL GRUPO DE FORMULA (III), SIENDO R4 H O UN GRUPO PROTECTOR. DE APLICACION COMO ANTIBACTERIANOS DE AMPLIO ESPECTRO EFICACES CONTRA BACTERIAS GRAM-POSITIVAS Y GRAM-NEGATIVAS.
ES542584A 1984-04-26 1985-04-25 Un derivado de 1,4-dihidro-4-oxonaftiridina Expired ES8700256A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59084963A JPS60228479A (ja) 1984-04-26 1984-04-26 1,4−ジヒドロ−4−オキソナフチリジン誘導体およびその塩

Publications (2)

Publication Number Publication Date
ES542584A0 ES542584A0 (es) 1986-09-16
ES8700256A1 true ES8700256A1 (es) 1986-09-16

Family

ID=13845280

Family Applications (2)

Application Number Title Priority Date Filing Date
ES542584A Expired ES8700256A1 (es) 1984-04-26 1985-04-25 Un derivado de 1,4-dihidro-4-oxonaftiridina
ES551538A Expired ES8706673A1 (es) 1984-04-26 1986-01-31 Un procedimiento para la preparacion de derivados de 1,4-dihidro-4-oxonaftiridina y sus sales

Family Applications After (1)

Application Number Title Priority Date Filing Date
ES551538A Expired ES8706673A1 (es) 1984-04-26 1986-01-31 Un procedimiento para la preparacion de derivados de 1,4-dihidro-4-oxonaftiridina y sus sales

Country Status (30)

Country Link
JP (1) JPS60228479A (es)
KR (1) KR870001693B1 (es)
AR (1) AR241911A1 (es)
AT (2) AT389698B (es)
AU (2) AU565087B2 (es)
BE (1) BE902279A (es)
CH (1) CH673458A5 (es)
CS (1) CS250684B2 (es)
DD (1) DD238795A5 (es)
DE (2) DE3514076A1 (es)
DK (1) DK165877C (es)
EG (1) EG17339A (es)
ES (2) ES8700256A1 (es)
FI (1) FI80453C (es)
FR (2) FR2563521B1 (es)
GB (2) GB2158825B (es)
HU (2) HU197571B (es)
ID (1) ID21142A (es)
IL (1) IL75021A (es)
IT (1) IT1209953B (es)
LU (1) LU85871A1 (es)
NL (2) NL187314C (es)
NO (1) NO162238C (es)
NZ (1) NZ211895A (es)
PH (3) PH22801A (es)
PL (1) PL147392B1 (es)
PT (1) PT80349B (es)
RO (2) RO95509B (es)
SE (2) SE463102B (es)
ZA (1) ZA853102B (es)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6172753A (ja) * 1984-09-18 1986-04-14 Dainippon Pharmaceut Co Ltd ピリジルケトン誘導体
AU576657B2 (en) * 1985-01-23 1988-09-01 Toyama Chemical Co. Ltd. Naphthyridine and pyridine derivatives
AT392789B (de) * 1985-01-23 1991-06-10 Toyama Chemical Co Ltd Verfahren zur herstellung von 1-substituierten aryl-1,4-dihydro-4-oxonaphthyridinderivaten
DE3525108A1 (de) * 1985-06-07 1986-12-11 Bayer Ag, 5090 Leverkusen Antibakteriell wirksame chinoloncarbonsaeureester
ATE75740T1 (de) * 1985-06-26 1992-05-15 Daiichi Seiyaku Co Pyridoncarbonsaeurederivate.
US4962112A (en) * 1987-08-04 1990-10-09 Abbott Laboratories 7-(2-methyl-4-aminopyrrolidinyl)naphthryidine and quinoline compounds
IE62600B1 (en) * 1987-08-04 1995-02-22 Abbott Lab Naphtyridine antianaerobic compounds
US4859776A (en) * 1988-03-11 1989-08-22 Abbott Laboratories (S)-7-(3-aminopyrrolidin-1-yl)-1-(ortho, para-difluorophenyl)-1,4-dihydro-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid and method for its preparation
JP2844079B2 (ja) * 1988-05-23 1999-01-06 塩野義製薬株式会社 ピリドンカルボン酸系抗菌剤
DE3934082A1 (de) * 1989-10-12 1991-04-18 Bayer Ag Chinoloncarbonsaeurederivate, verfahren zu ihrer herstellung sowie ihre verwendung als antivirale mittel
AU1161492A (en) * 1991-01-14 1992-08-17 Hanmi Pharmaceutical Co., Ltd. Novel quinolone compounds and processes for preparation thereof
FR2692577B1 (fr) * 1992-05-26 1996-02-02 Bouchara Sa Nouvelles quinolones fluorees, leur procede de preparation et les compositions pharmaceutiques en renfermant.
KR940014395A (ko) * 1992-12-09 1994-07-18 강박광 신규한 퀴놀론 유도체 및 그의 제조방법
KR0148277B1 (ko) * 1993-01-18 1998-11-02 채영복 신규한 플루오르퀴놀론계 유도체 및 그의 제조방법
AU4272793A (en) * 1993-04-24 1994-11-21 Korea Research Institute Of Chemical Technology Novel quinolone carboxylic acid derivatives and process for preparing the same
KR950018003A (ko) * 1993-12-09 1995-07-22 스미스클라인 비참 피엘씨 신규한 퀴놀론 유도체 및 그의 제조 방법
DE69531305T2 (de) * 1994-10-20 2004-05-13 Wakunaga Seiyaku K.K. Pyridoncarboxylat- derivate oder salze davon und antibakterielle zusammensetzungen die diese als aktiven bestandteil enthalten
WO1997040036A1 (fr) 1996-04-19 1997-10-30 Wakunaga Pharmaceutical Co., Ltd. Nouveaux derives de l'acide pyridonocarboxylique ou des sels de cet acide et agents antibacteriens contenant ces substances en tant que composant actif
KR20000052892A (ko) * 1996-10-30 2000-08-25 빌프리더 하이더 나프티리딘 화합물의 제조 방법 및 신규 중간 생성물
DE19713506A1 (de) 1997-04-01 1998-10-08 Bayer Ag Verfahren zur Herstellung von 2,6-Dichlor-5-fluornicotinonitril und die chemische Verbindung 3-Cyano-2-hydroxy-5-fluorpyrid-6-on-mononatriumsalz sowie dessen Tautomere
KR100768034B1 (ko) 1999-03-17 2007-10-17 다이이찌 세이야꾸 가부시기가이샤 의약 조성물
US6441182B1 (en) 1999-06-10 2002-08-27 Bayer Aktiengesellschaft Method for the production of 2,6-dichloro-5-fluoro-nicotinic acid and coarse and particularly pure 2,6-dichloro-5-fluoro-nicotinic acid
WO2001017991A1 (fr) 1999-09-02 2001-03-15 Wakunaga Pharmaceutical Co., Ltd. Derive d'acide quinolinecarboxylique ou son sel
EP1313708A1 (en) * 2000-08-29 2003-05-28 Chiron Corporation Quinoline antibacterial compounds and methods of use thereof
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
CN101792443A (zh) * 2010-03-09 2010-08-04 北京欧凯纳斯科技有限公司 氟代喹诺酮衍生物及其制备方法和用途
JOP20190045A1 (ar) 2016-09-14 2019-03-14 Bayer Ag مركبات أميد حمض 1- أريل-نفثيريدين-3-كربوكسيليك مستبدلة في الموضع 7 واستخدامها.
CN114369092A (zh) * 2021-12-20 2022-04-19 赤峰万泽药业股份有限公司 甲苯磺酸妥舒沙星及其制备方法

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2125310A1 (en) * 1971-05-21 1972-11-30 Sterling Drug Inc , New York, NY (V St A) 1-alkyl-1,4-dihydro-4-oxo-1,8-naphtyridine 3-carboxylic acids antibac
AR223983A1 (es) * 1978-08-25 1981-10-15 Dainippon Pharmaceutical Co Un procedimiento para-preparar derivados de acido 6-halogeno-4-oxo-7-(1-piperazinil)-1,8-naftiridin-3-carboxilico
DE3033157A1 (de) * 1980-09-03 1982-04-01 Bayer Ag, 5090 Leverkusen 7-amino-1-cyclopropyl-4-oxo-1,4-dihydro-naphthyridin-3-carbonsaeuren, verfahren zu ihrer herstellung sowie diese enthaltende antibakterielle mittel
US4382937A (en) * 1981-02-27 1983-05-10 Dainippon Pharmaceutical Co., Ltd. Naphthyridine derivatives and their use as anti-bacterials
IE55898B1 (en) * 1982-09-09 1991-02-14 Warner Lambert Co Antibacterial agents
NZ210847A (en) * 1984-01-26 1988-02-29 Abbott Lab Naphthyridine and pyridopyrimidine derivatives and pharmaceutical compositions
IL74064A (en) * 1984-01-26 1988-09-30 Abbott Lab 1,7-disubstituted-1,4-dihydro-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid derivatives and antibacterial compositions containing them
AU576657B2 (en) * 1985-01-23 1988-09-01 Toyama Chemical Co. Ltd. Naphthyridine and pyridine derivatives
DE3525108A1 (de) * 1985-06-07 1986-12-11 Bayer Ag, 5090 Leverkusen Antibakteriell wirksame chinoloncarbonsaeureester

Also Published As

Publication number Publication date
RO91871B (ro) 1987-07-31
ATA267888A (de) 1989-09-15
GB8510297D0 (en) 1985-05-30
CH673458A5 (es) 1990-03-15
PH25046A (en) 1991-01-28
FR2563521A1 (fr) 1985-10-31
DK185685D0 (da) 1985-04-25
CS250684B2 (en) 1987-05-14
NO162238C (no) 1989-12-06
ES542584A0 (es) 1986-09-16
GB2158825A (en) 1985-11-20
IT1209953B (it) 1989-08-30
AU612993B2 (en) 1991-07-25
PT80349B (pt) 1987-09-30
IT8548002A0 (it) 1985-04-26
DE3514076A1 (de) 1985-10-31
SE463102B (sv) 1990-10-08
FR2614620A1 (fr) 1988-11-04
FI851637A0 (fi) 1985-04-25
ES8706673A1 (es) 1987-07-01
GB2191776A (en) 1987-12-23
PL253108A1 (en) 1985-12-17
NZ211895A (en) 1988-07-28
IL75021A0 (en) 1985-08-30
HUT38634A (en) 1986-06-30
AT389698B (de) 1990-01-10
KR870001693B1 (ko) 1987-09-24
SE8804586L (sv) 1988-12-20
KR850007596A (ko) 1985-12-07
DK165877C (da) 1993-06-21
FI80453C (fi) 1990-06-11
IL75021A (en) 1994-01-25
SE8502017D0 (sv) 1985-04-25
RO91871A (ro) 1987-07-30
AU8180487A (en) 1988-03-24
FR2614620B1 (fr) 1990-03-09
GB2191776B (en) 1990-03-28
BE902279A (fr) 1985-10-25
GB8716897D0 (en) 1987-08-26
NL187314C (nl) 1991-08-16
DE3514076C2 (es) 1989-03-30
DK185685A (da) 1985-10-27
SE8502017L (sv) 1985-10-27
AT390258B (de) 1990-04-10
FI80453B (fi) 1990-02-28
SE8804586D0 (sv) 1988-12-20
PH25228A (en) 1991-03-27
RO95509A (ro) 1988-09-30
ID21142A (id) 1999-04-29
AU565087B2 (en) 1987-09-03
RO95509B (ro) 1988-10-01
DD238795A5 (de) 1986-09-03
PL147392B1 (en) 1989-05-31
AR241911A1 (es) 1993-01-29
NO851643L (no) 1985-10-28
PT80349A (en) 1985-05-01
DK165877B (da) 1993-02-01
PH22801A (en) 1988-12-12
FI851637L (fi) 1985-10-27
JPS6320828B2 (es) 1988-04-30
SE501412C2 (sv) 1995-02-13
HU197571B (en) 1989-04-28
EG17339A (en) 1989-06-30
NL9100648A (nl) 1991-08-01
NO162238B (no) 1989-08-21
ZA853102B (en) 1986-12-30
LU85871A1 (en) 1985-12-16
GB2158825B (en) 1989-01-25
ES551538A0 (es) 1987-07-01
JPS60228479A (ja) 1985-11-13
FR2563521B1 (fr) 1989-02-03
AU4165085A (en) 1985-10-31
HU194226B (en) 1988-01-28
NL8501172A (nl) 1985-11-18
ATA122485A (de) 1989-06-15
DE3546658C2 (es) 1992-04-02

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FD1A Patent lapsed

Effective date: 20060612