BE1003252A4 - Derives d'acide pyridone carboxylique et leurs sels, leur procede de fabrication et agents antibacteriens les comprenant. - Google Patents
Derives d'acide pyridone carboxylique et leurs sels, leur procede de fabrication et agents antibacteriens les comprenant. Download PDFInfo
- Publication number
- BE1003252A4 BE1003252A4 BE8900452A BE8900452A BE1003252A4 BE 1003252 A4 BE1003252 A4 BE 1003252A4 BE 8900452 A BE8900452 A BE 8900452A BE 8900452 A BE8900452 A BE 8900452A BE 1003252 A4 BE1003252 A4 BE 1003252A4
- Authority
- BE
- Belgium
- Prior art keywords
- lower alkyl
- protected
- amino
- unprotected
- salts
- Prior art date
Links
- 239000003242 anti bacterial agent Substances 0.000 title abstract 2
- YSLIPUSJNFIFAB-UHFFFAOYSA-N 2-oxopyridine-1-carboxylic acid Chemical class OC(=O)N1C=CC=CC1=O YSLIPUSJNFIFAB-UHFFFAOYSA-N 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 150000003839 salts Chemical class 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 13
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 4
- 125000003282 alkyl amino group Chemical group 0.000 abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- SQMFHXCAROIIPN-UHFFFAOYSA-N 2h-pyrido[2,3-h][1,2]benzothiazine Chemical compound 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 compound C1=CC2=NC=CC=C2C2=C1C=CNO2 QDEJGQKJMKXYLM-UHFFFAOYSA-N 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000001118 alkylidene group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000001841 imino group Chemical group [H]N=* 0.000 abstract 1
- 125000006239 protecting group Chemical group 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
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
Abstract
Ce composé (I), qui est un agent antibactérien, a un groupe cyclopropyle substitué ou non en position 10 d'un noyau pyridobenzoxazine, pyridobenzothiazine ou pyridoquinoxaline : R1 = H ou groupe protecteur de carboxyle; R2 = H, Hal, alcoxy, hydroxyle protégé ou non, amino protégé ou non, alkylamino inférieur protégé ou non ou di-(alkyl inférieur) amino; R3 = moins l'un parmi H, alkyl inférieur, amino protégé ou non, alkylamino inférieur protégé ou non, di-(alkyl inférieur)amino, carboxyle protégé ou non, amino-alkyl inférieur protégé ou non, (alkyl inférieur)amino-(alkyl inférieur) protégé ou non, di-(alkyl inférieur) amino-(alkyl inférieur) et hydroxy-(alkyl inférieur) protégé ou non ; R4 = au moins l'un parm H, alkyl inférieur, halogéno-(alkyl inférieur), hydroxy-(alkyl inférieur) protégé ou non, alkylidène inférieur et un groupe formant un noyau cycloalcane avec l'atome de C auquel R4 se rattache; X= Hal; et A=O ou S, imino substitué par alkyl inférieur ou non-substitué.
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 (1)
Publication Number | Publication Date |
---|---|
BE1003252A4 true BE1003252A4 (fr) | 1992-02-11 |
Family
ID=26417038
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE8900452A BE1003252A4 (fr) | 1988-04-23 | 1989-04-24 | Derives d'acide pyridone carboxylique et leurs sels, leur procede de fabrication et agents antibacteriens les comprenant. |
Country Status (21)
Country | Link |
---|---|
US (1) | US4990508A (fr) |
JP (1) | JPH0228178A (fr) |
KR (1) | KR910005833B1 (fr) |
AT (1) | AT398422B (fr) |
AU (1) | AU601324B2 (fr) |
BE (1) | BE1003252A4 (fr) |
CA (1) | CA1340493C (fr) |
CH (1) | CH680793A5 (fr) |
DE (1) | DE3913245C2 (fr) |
DK (1) | DK175649B1 (fr) |
ES (1) | ES2016012A6 (fr) |
FI (1) | FI91529C (fr) |
FR (1) | FR2630441B1 (fr) |
GB (1) | GB2217710B (fr) |
HU (2) | HU205759B (fr) |
IL (1) | IL89931A (fr) |
IT (1) | IT1231760B (fr) |
NL (1) | NL192832C (fr) |
NO (1) | NO171214C (fr) |
NZ (1) | NZ228847A (fr) |
SE (1) | SE504625C2 (fr) |
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 (fr) * | 1988-10-24 | 2000-05-03 | PROCTER & GAMBLE PHARMACEUTICALS, INC. | Lactam-quinolones antimicrobiennes |
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 (fr) * | 1993-08-27 | 1995-07-21 | Hokuriku Pharmacetical Co Ltd | |
IT1270834B (it) * | 1993-10-27 | 1997-05-13 | Archimica Spa | Disolfuro chinolico |
IT1270836B (it) * | 1993-10-27 | 1997-05-13 | Archimica Spa | Procedimento per la preparazione di rufloxacina e suoi sali |
USH1480H (en) * | 1993-12-09 | 1995-09-05 | The Procter & Gamble Company | Methods of using dyphylline for the promotion of hair growth |
KR100768034B1 (ko) | 1999-03-17 | 2007-10-17 | 다이이찌 세이야꾸 가부시기가이샤 | 의약 조성물 |
KR20040105772A (ko) | 2002-03-21 | 2004-12-16 | 바스프 악티엔게젤샤프트 | 살진균성 트리아졸로피리미딘, 이의 제조방법 및 유해진균 방제를 위한 이의 용도 및 상기 성분을 함유하는조성물 |
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 |
PL2383271T3 (pl) * | 2006-03-13 | 2013-12-31 | Kyorin Seiyaku Kk | Aminochinolony jako inhibitory GSK-3 |
EP2203458B1 (fr) * | 2007-09-11 | 2011-11-02 | Kyorin Pharmaceutical Co., Ltd. | Cyanoaminoquinolones en tant qu'inhibiteurs de gsk-3 |
CA2699152C (fr) | 2007-09-12 | 2015-11-24 | Activx Biosciences, Inc. | Aminoquinolones spirocycliques utilisees en tant qu'inhibiteurs de gsk-3 |
JP5502889B2 (ja) * | 2009-03-11 | 2014-05-28 | 杏林製薬株式会社 | gsk−3阻害剤としての7−シクロアルキルアミノキノロン |
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 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0206101A1 (fr) * | 1985-06-22 | 1986-12-30 | Bayer Ag | Procédé pour la préparation d'acides quinolone-4 carboxyliques-3 pontés entre les positions 1,8 |
JPH0193573A (ja) * | 1987-10-05 | 1989-04-12 | Toyama Chem Co Ltd | 新規なキノリン誘導体およびその塩 |
Family Cites Families (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
US4607032A (en) * | 1984-04-26 | 1986-08-19 | Abbott Laboratories | Quino-benoxazine antibacterial compounds |
US4540694A (en) * | 1984-04-26 | 1985-09-10 | Abbott Laboratories | 1-Pyridine substituted quino-benoxazines and antibacterial use |
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 |
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 |
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 CA CA000596351A patent/CA1340493C/fr not_active Expired - Lifetime
- 1989-04-11 GB GB8908096A patent/GB2217710B/en not_active Expired - Lifetime
- 1989-04-12 AU AU32661/89A patent/AU601324B2/en not_active Expired
- 1989-04-12 IL IL89931A patent/IL89931A/xx unknown
- 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 ES ES8901409A patent/ES2016012A6/es not_active Expired - Fee Related
- 1989-04-21 FR FR898905335A patent/FR2630441B1/fr not_active Expired - Lifetime
- 1989-04-21 AT AT0095989A patent/AT398422B/de not_active IP Right Cessation
- 1989-04-21 DE DE3913245A patent/DE3913245C2/de not_active Expired - Lifetime
- 1989-04-21 NZ NZ228847A patent/NZ228847A/en unknown
- 1989-04-21 SE SE8901464A patent/SE504625C2/sv 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 FI FI891910A patent/FI91529C/fi not_active IP Right Cessation
- 1989-04-21 IT IT8947875A patent/IT1231760B/it active
- 1989-04-21 CH CH1530/89A patent/CH680793A5/de not_active IP Right Cessation
- 1989-04-21 KR KR1019890005253A patent/KR910005833B1/ko not_active IP Right Cessation
- 1989-04-21 NL NL8901007A patent/NL192832C/nl not_active IP Right Cessation
- 1989-04-24 BE BE8900452A patent/BE1003252A4/fr not_active IP Right Cessation
-
1995
- 1995-06-30 HU HU95P/P00674P patent/HU211568A9/hu unknown
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0206101A1 (fr) * | 1985-06-22 | 1986-12-30 | Bayer Ag | Procédé pour la préparation d'acides quinolone-4 carboxyliques-3 pontés entre les positions 1,8 |
JPH0193573A (ja) * | 1987-10-05 | 1989-04-12 | Toyama Chem Co Ltd | 新規なキノリン誘導体およびその塩 |
Non-Patent Citations (1)
Title |
---|
CHEMICAL ABSTRACTS, vol. 111, no. 19, 6 novembre 1989, page 714, résumé no. 174003d, Columbus, Ohio, US; & JP-A-01 93 573 (TOYAMA CHEMICAL CO.) 12-04-1989 * |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
RE20 | Patent expired |
Owner name: *TOYAMA CHEMICAL CO. LTD Effective date: 20090424 |