ES2135372T3 - Derivados del acido piridonacarboxilico opticamente activos. - Google Patents

Derivados del acido piridonacarboxilico opticamente activos.

Info

Publication number
ES2135372T3
ES2135372T3 ES89107550T ES89107550T ES2135372T3 ES 2135372 T3 ES2135372 T3 ES 2135372T3 ES 89107550 T ES89107550 T ES 89107550T ES 89107550 T ES89107550 T ES 89107550T ES 2135372 T3 ES2135372 T3 ES 2135372T3
Authority
ES
Spain
Prior art keywords
derivatives
pyridonacarboxylic
acid
optically active
halogenocide
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 - Lifetime
Application number
ES89107550T
Other languages
English (en)
Inventor
Isao Hayakawa
Youichi Kimura
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.)
Daiichi Pharmaceutical Co Ltd
Original Assignee
Daiichi Pharmaceutical 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
Application filed by Daiichi Pharmaceutical Co Ltd filed Critical Daiichi Pharmaceutical Co Ltd
Application granted granted Critical
Publication of ES2135372T3 publication Critical patent/ES2135372T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
    • C07D215/48Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C07D215/54Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
    • C07D215/56Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3 with oxygen atoms in position 4
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • 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
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/04Heterocyclic 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Oncology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Communicable Diseases (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyridine Compounds (AREA)
  • Quinoline Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Hydrogenated Pyridines (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

DERIVADOS DE ACIDOS PIRIDONE CARBOXILICO SUSTITUIDOS - N1 - (1, 2 - CIS - 2 - HALOGENOCIDO PROPIL) REPRESENTADOS POR LA FORMULA (I) Y LAS SALES DE ELLO SON DESCUBIERTOS. ESOS COMPONENTES TIENEN ACTIVIDADES ANTIBACTERIALES PATENTES CONTRA UNA ANCHA VARIEDAD DE BACTERIAS INFECCIOSAS, Y SON UTILES COMO AGENTES ANTIBACTERIALES POR ADMINISTRACION ORAL O PARENTERAL.
ES89107550T 1988-04-27 1989-04-26 Derivados del acido piridonacarboxilico opticamente activos. Expired - Lifetime ES2135372T3 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP10462588 1988-04-27
JP29698488 1988-11-24

Publications (1)

Publication Number Publication Date
ES2135372T3 true ES2135372T3 (es) 1999-11-01

Family

ID=26445063

Family Applications (1)

Application Number Title Priority Date Filing Date
ES89107550T Expired - Lifetime ES2135372T3 (es) 1988-04-27 1989-04-26 Derivados del acido piridonacarboxilico opticamente activos.

Country Status (25)

Country Link
US (4) US5587386A (es)
EP (1) EP0341493B1 (es)
JP (5) JP2714597B2 (es)
KR (1) KR0184614B1 (es)
CN (1) CN1033751C (es)
AT (1) ATE182145T1 (es)
AU (1) AU625414B2 (es)
BG (1) BG61122B2 (es)
CA (1) CA1340801C (es)
DE (1) DE68929030T2 (es)
DK (1) DK175467B1 (es)
ES (1) ES2135372T3 (es)
FI (1) FI96947C (es)
GR (1) GR3031365T3 (es)
HU (1) HU211136A9 (es)
IL (1) IL90062A (es)
LV (1) LV10092B (es)
MY (1) MY105136A (es)
NO (1) NO175939C (es)
NZ (1) NZ228893A (es)
PT (1) PT90377B (es)
RU (1) RU2075475C1 (es)
SG (1) SG48036A1 (es)
UA (1) UA29378C2 (es)
YU (1) YU48432B (es)

Families Citing this family (43)

* Cited by examiner, † Cited by third party
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MY105136A (en) * 1988-04-27 1994-08-30 Daiichi Seiyaku Co Optically active pyridonecarboxylic acid derivatives.
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
CA1336090C (en) * 1988-08-31 1995-06-27 Isao Hayakawa Spiro-substituted cyclic amines of quinolone derivatives
EP0443498A1 (en) * 1990-02-19 1991-08-28 Kyorin Pharmaceutical Co., Ltd. Isoindoline derivatives
MY109714A (en) * 1990-10-18 1997-04-30 Daiichi Seiyaku Co Process for preparing 8-chloroquinolone derivatives
US5696132A (en) * 1991-05-28 1997-12-09 Daiichi Pharmaceutical Co., Ltd. Pyridonecarboxylic acid derivatives
CA2111463C (en) * 1991-06-19 1997-08-26 Bingwei V. Yang Azaspiro quinolone antibacterial agents
KR960011370B1 (ko) * 1991-12-31 1996-08-22 재단법인 한국화학연구소 스피로알킬아민 유도체와 그의 제조방법
JP3268098B2 (ja) * 1992-12-25 2002-03-25 第一製薬株式会社 二環性環状アミン誘導体
ZA946853B (en) * 1993-09-10 1995-04-24 Daiichi Seiyaku Co Crystals of antimicrobial compound.
CA2194435A1 (en) * 1994-07-18 1996-02-01 Ube Industries, Ltd. Trifluoromethylquinolinecarboxylic acid derivative
DK0807630T3 (da) * 1995-02-02 2003-09-01 Daiichi Seiyaku Co Heterocykliske forbindelser
WO1996024593A1 (en) 1995-02-07 1996-08-15 Daiichi Pharmaceutical Co., Ltd. Heterocyclic spiro derivatives
JPH09124556A (ja) 1995-08-30 1997-05-13 Dai Ichi Seiyaku Co Ltd ハロゲン化シクロプロパン誘導体の製造方法
US6121285A (en) 1995-11-22 2000-09-19 Daiichi Pharmaceutical Co., Ltd. Substituted aminocycloalkylpyrrolidine derivatives and cis-substituted aminocycloalkylpyrrolidine derivatives
DE69635812T2 (de) * 1995-11-22 2006-10-19 Daiichi Pharmaceutical Co., Ltd. Substituierte aminocycloalkylpyrrolidinderivate
WO1997029102A1 (en) * 1996-02-09 1997-08-14 Toyama Chemical Co., Ltd. Quinolonecarboxylic acid derivatives or salts thereof
TW425394B (en) * 1996-04-24 2001-03-11 Daiichi Seiyaku Co Antimicrobial quinolone derivatives having 3-(N-cycloalkyl) aminomethylpyrrolidine group
WO1998024781A1 (en) * 1996-12-04 1998-06-11 Daiichi Pharmaceutical Co., Ltd. Substituted aminomethylpyrrolidine derivatives
BR9915599A (pt) * 1998-11-24 2001-11-20 Daiichi Seiyaku Co Derivados de aminometilpirrolidina substituìdacom cicloalquila
DE60011264T2 (de) * 1999-03-10 2005-07-14 Daiichi Pharmaceutical Co., Ltd. Aminomethylpyrrolidin-derivate mit aromatischen substituenten
CA2367373C (en) 1999-03-17 2011-09-20 Daiichi Pharmaceutical Co., Ltd. Medicinal compositions
ATE407121T1 (de) * 2000-02-09 2008-09-15 Daiichi Sankyo Co Ltd Gegen säurebeständige bakterien wirksame antibakterielle mittel die pyridincarbonsäuren als aktiven wirkstoff enthalten
AU2001244671B2 (en) * 2000-03-31 2005-01-27 Daiichi Pharmaceutical Co., Ltd. Quinolonecarboxylic acid derivative
ATE396729T1 (de) 2000-04-24 2008-06-15 Daiichi Sankyo Co Ltd Stabile flüssige zubereitung enthaltend sitafloxacin
RU2287328C2 (ru) 2000-08-08 2006-11-20 Дайити Фармасьютикал Ко.,Лтд. Твердый препарат с высоким всасыванием
WO2003097634A1 (en) * 2002-05-17 2003-11-27 Daiichi Pharmaceutical Co., Ltd. Process for producing quinolonecarboxylic acid derivative
JP4413864B2 (ja) * 2003-01-07 2010-02-10 第一三共株式会社 還元的脱ハロゲン化方法
US7085154B2 (en) * 2003-06-03 2006-08-01 Samsung Electronics Co., Ltd. Device and method for pulse width control in a phase change memory device
EP1757598A4 (en) * 2004-05-13 2010-07-21 Daiichi Seiyaku Co SUBSTITUTED PYRROLIDINE DERIVATIVE
US7563805B2 (en) 2005-05-19 2009-07-21 Daiichi Pharmaceutical Co., Ltd. Tri-, tetra-substituted-3-aminopyrrolidine derivative
JP5063032B2 (ja) * 2005-05-19 2012-10-31 第一三共株式会社 トリ−、テトラ−置換−3−アミノピロリジン誘導体
RU2420524C2 (ru) * 2005-05-19 2011-06-10 Дайити Санкио Компани, Лимитед Производные три- или тетра-замещенного-3-аминопирролидина
US7928232B2 (en) * 2005-05-20 2011-04-19 Daiichi Sankyo Company, Limited Method for producing asymmetric tetrasubstituted carbon atom-containing compound
US7977346B2 (en) 2006-01-17 2011-07-12 Guoqing Paul Chen Spiro compounds and methods of use
TWI386401B (zh) * 2006-03-27 2013-02-21 Daiichi Seiyaku Co 醫藥用水合物
MX2009007291A (es) 2007-01-05 2009-07-14 Daiichi Sankyo Co Ltd Derivado de aminopirrolidina sustituido fusionado.
CN102089439B (zh) 2008-07-11 2013-11-13 住友化学株式会社 (1s,2r)-2-氯-2-氟环丙烷羧酸的制造方法
FR2961207B1 (fr) * 2010-06-09 2013-01-18 Oreal Utilisation d'un derive de 4- carboxy 2-pyrrolidinone comme solvant dans les compositions cosmetiques ; compositions cosmetiques les contenant ; nouveaux composes
CN103467448B (zh) * 2013-09-18 2015-04-15 浙江司太立制药股份有限公司 7-(3-氨基-4-烷氧亚胺基-1-哌啶基)-1-[(1r,2s)-2-氟环丙基]喹诺酮羧酸类化合物及其制备方法
EP2957561A1 (en) * 2014-06-18 2015-12-23 Université Paris 6 Pierre et Marie Curie UPMC Novel fluoroquinolones and use thereof to treat bacterial infections
CN105330590B (zh) * 2015-10-15 2018-09-25 广州市朗启医药科技有限责任公司 西他沙星五元环侧链中间体的制备方法
CN109912504B (zh) * 2019-04-04 2020-11-10 山东省联合农药工业有限公司 一种喹啉羧酸类化合物及其制备方法与用途

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6212760A (ja) * 1984-12-14 1987-01-21 Dai Ichi Seiyaku Co Ltd 1−(2−ハロゲノシクロプロピル)キノリンカルボン酸誘導体
HUT40639A (en) * 1985-03-08 1987-01-28 Kyorin Seiyaku Kk Process for producing quinolon-carboxylic acid derivative and pharmaceutical composition containing them
DE3509546A1 (de) * 1985-03-16 1986-09-25 Bayer Ag, 5090 Leverkusen 7-amino-1-(subst.cyclopropyl)-1,4-dihydro-4-oxo-3-chinolincarbonsaeuren, verfahren zu ihrer herstellung sowie diese enthaltende antibakterielle mittel
US4657913A (en) 1985-04-18 1987-04-14 Warner-Lambert Company Trifluoro- quinoline -3- carboxylic acids and their use as anti-bacterial agents
US4668680A (en) * 1985-12-12 1987-05-26 Warner-Lambert Company 5-amino-6,8-difluoroquinolones as antibacterial agents
US4735949A (en) 1986-02-18 1988-04-05 Warner-Lambert Company Disubstituted-7-pyrrolidinonaphthyridine antibacterial agents
DE3705621C2 (de) * 1986-02-25 1997-01-09 Otsuka Pharma Co Ltd Heterocyclisch substituierte Chinoloncarbonsäurederivate
DE3702393A1 (de) * 1987-01-28 1988-08-11 Bayer Ag 8-cyano-1-cyclopropyl-1,4-dihydro-4-oxo- 3-chinolincarbonsaeuren, verfahren zu ihrer herstellung und diese enthaltende antibakterielle mittel
US5290934A (en) * 1987-04-16 1994-03-01 Otsuka Pharmaceutical Company, Limited Benzoheterocyclic compounds
US4851418A (en) * 1987-08-21 1989-07-25 Warner-Lambert Company Naphthyridine antibacterial agents containing an α-amino acid in the side chain of the 7-substituent
MY105136A (en) * 1988-04-27 1994-08-30 Daiichi Seiyaku Co Optically active pyridonecarboxylic acid derivatives.
FI95130C (fi) * 1988-07-20 1995-12-27 Sankyo Co Menetelmä lääkeaineena käyttökelpoisten 4-oksokinoliini-3-karboksyylihapon johdannaisten valmistamiseksi
US5286723A (en) 1988-08-31 1994-02-15 Daiichi Seiyaku Co., Ltd. Spiro compound
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
AU2001244671B2 (en) 2000-03-31 2005-01-27 Daiichi Pharmaceutical Co., Ltd. Quinolonecarboxylic acid derivative
EP1757598A4 (en) * 2004-05-13 2010-07-21 Daiichi Seiyaku Co SUBSTITUTED PYRROLIDINE DERIVATIVE

Also Published As

Publication number Publication date
EP0341493A3 (en) 1990-12-19
BG61122B2 (bg) 1996-11-29
NO891698L (no) 1989-10-30
USRE41149E1 (en) 2010-02-23
FI891980A7 (fi) 1989-10-28
HU211136A9 (en) 1995-10-30
DK205789A (da) 1989-10-28
YU87589A (en) 1990-12-31
KR900016205A (ko) 1990-11-12
NO175939C (no) 1995-01-04
FI891980A0 (fi) 1989-04-26
US5767127A (en) 1998-06-16
DK205789D0 (da) 1989-04-27
MY105136A (en) 1994-08-30
DE68929030T2 (de) 2000-03-23
IL90062A (en) 1994-10-07
UA29378C2 (uk) 2000-11-15
AU625414B2 (en) 1992-07-09
IL90062A0 (en) 1989-12-15
JPH11124367A (ja) 1999-05-11
RU2075475C1 (ru) 1997-03-20
JPH11124380A (ja) 1999-05-11
AU3370289A (en) 1989-11-02
US5587386A (en) 1996-12-24
FI96947C (fi) 1996-09-25
NO891698D0 (no) 1989-04-25
SG48036A1 (en) 1998-04-17
HK1002108A1 (en) 1998-07-31
NO175939B (no) 1994-09-26
US6031102A (en) 2000-02-29
PT90377B (pt) 1994-09-30
JPH1067779A (ja) 1998-03-10
ATE182145T1 (de) 1999-07-15
CN1033751C (zh) 1997-01-08
NZ228893A (en) 1990-06-26
JP2714597B2 (ja) 1998-02-16
JP2903292B2 (ja) 1999-06-07
CN1037507A (zh) 1989-11-29
GR3031365T3 (en) 2000-01-31
DE68929030D1 (de) 1999-08-19
EP0341493B1 (en) 1999-07-14
KR0184614B1 (ko) 1999-05-01
PT90377A (pt) 1989-11-10
JPH02231475A (ja) 1990-09-13
CA1340801C (en) 1999-10-26
YU48432B (sh) 1998-07-10
EP0341493A2 (en) 1989-11-15
LV10092B (en) 1995-02-20
JP2917010B2 (ja) 1999-07-12
DK175467B1 (da) 2004-11-01
FI96947B (fi) 1996-06-14
JPH07300416A (ja) 1995-11-14

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