AR245450A1 - Procedimiento para preparar nuevos derivados de 4-piridona y sus sales y esteres aceptables desde el punto de vista fisiologico. - Google Patents
Procedimiento para preparar nuevos derivados de 4-piridona y sus sales y esteres aceptables desde el punto de vista fisiologico.Info
- Publication number
- AR245450A1 AR245450A1 AR87308059A AR30805987A AR245450A1 AR 245450 A1 AR245450 A1 AR 245450A1 AR 87308059 A AR87308059 A AR 87308059A AR 30805987 A AR30805987 A AR 30805987A AR 245450 A1 AR245450 A1 AR 245450A1
- Authority
- AR
- Argentina
- Prior art keywords
- formula
- hydrogen
- compounds
- group
- alkyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/80—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D211/84—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen directly attached to ring carbon atoms
- C07D211/86—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/08—Bridged 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
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)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
PROCEDIMIENTO PARA PREPARAR DERIVADOS DE 4-PIRIDONA, DE FORMULA (I), EN LA QUE R1 ES 2,4-DIFLUOROFENILO;R2 ES HIDROGENO O S UNIDO AL N DEL CICLO A TRAVES DE UN PUENTE DE ETILENO; X ES HIDROGENO;Y ES UNA BASE DE FORMULA (IIA) O (IIB), DONDE R3 ES HIDROGENO, ALQUILO, BENCILO, FORMILO, ACETONILO O UN RESTO DE FORMULA (III), DONDE A) SE HACEN REACCIONAR COMPUESTOS DE FORMULA (IV) EN LA QUE L ES CLORO O FLUOR, Y R4 ES HIDROGENO, ALQUILO O UN COMPLEJO DE BORO DE FORMULA -B(R5R6), DONDE R5 Y R6 SON IGUALES, Y SON FLUOR O RESTOS -O(CO)ALQUILO, CON COMPUESTOS DE FORMULA (VA) O (VB) EN LAQUE R3' ES IGUAL A R3 O ES UN GRUPO PROTECTOR, Y A CONTINUACION, B) EN LOS COMPUESTOS ASI OBTENIDOS, PARA LOS QUE R4 ALQUILO O UN GRUPO -B(R6R5), SE ELIMINA EL GRUPO -B(R5R6) O EL ALQUILO MEDIANTE UN HIDROXIDO ACUOSO O UNA BASE ORGANICA, PARA OBTENER COMPUESTOS DE FORMULA (I) EN LA QUE X ES HIDROGENO; C) SE ELIMINA EL GRUPO PROTECTOR DEL AMINO, EN R3'; D) LOS COMPUESTOS OBTENIDOS, DE FORMULA (I) EN LA QUE R 3 ES HIDROGENO, EVENTUALMENTE SE METILAN, BENCILAN, FORMILAN O SE HACEN REACCIONAR CON BROMOACETONA O CON UN COMPUESTO DE FORMULA R7HAL, EN LA QUE R7 ES EL RESTO DE FORMULA (III).
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3622509 | 1986-07-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR245450A1 true AR245450A1 (es) | 1994-01-31 |
Family
ID=6304401
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AR87308059A AR245450A1 (es) | 1986-07-04 | 1987-07-03 | Procedimiento para preparar nuevos derivados de 4-piridona y sus sales y esteres aceptables desde el punto de vista fisiologico. |
Country Status (24)
Country | Link |
---|---|
US (1) | US5045549A (es) |
EP (1) | EP0251308B1 (es) |
JP (1) | JPH07103123B2 (es) |
KR (1) | KR880001595A (es) |
AR (1) | AR245450A1 (es) |
AT (1) | ATE58538T1 (es) |
AU (1) | AU608515B2 (es) |
CS (1) | CS277415B6 (es) |
DD (1) | DD262428A1 (es) |
DE (1) | DE3766299D1 (es) |
DK (1) | DK342187A (es) |
ES (1) | ES2018667B3 (es) |
FI (1) | FI88506C (es) |
GR (1) | GR3001097T3 (es) |
HU (1) | HU197907B (es) |
IL (1) | IL83049A (es) |
MY (1) | MY101261A (es) |
NO (1) | NO166130C (es) |
NZ (1) | NZ220950A (es) |
PH (1) | PH24239A (es) |
PT (1) | PT85257B (es) |
SU (1) | SU1551248A3 (es) |
YU (1) | YU45039B (es) |
ZA (1) | ZA874849B (es) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IN166416B (es) * | 1985-09-18 | 1990-05-05 | Pfizer | |
YU46451B (sh) * | 1987-04-08 | 1993-10-20 | Chinoin Gyogyszer Es Vegyeszeti Ter Mekek Gyara Rt. | Postupak za dobivanje mešovitih anhidrida hinolin-karboksilne i borne kiseline |
JPH02131453A (ja) * | 1988-04-15 | 1990-05-21 | Asahi Glass Co Ltd | 2―クロロ―4,5―ジフルオロベンゾイルアクリル酸誘導体 |
JPH072679B2 (ja) * | 1988-04-15 | 1995-01-18 | 旭硝子株式会社 | 2―クロロ―4,5―ジフルオロ安息香酸誘導体 |
WO1989012055A1 (en) * | 1988-06-08 | 1989-12-14 | Kyorin Pharmaceutical Co., Ltd. | Antitumor agent |
JPH02298946A (ja) * | 1989-05-15 | 1990-12-11 | Johoku Seihan Center:Kk | 製版・版下作製材および製版・版下作製における貼付方法 |
EP0449445A3 (en) * | 1990-03-27 | 1993-08-25 | Pfizer Inc. | Preparation of beta-ketoesters useful in preparing quinolone antibiotics |
JPH05506033A (ja) | 1990-04-18 | 1993-09-02 | ノーウィッチ、イートン、ファーマスーティカルズ、インコーポレーテッド | 抗微生物性キノロニルラクタム類 |
FR2692577B1 (fr) * | 1992-05-26 | 1996-02-02 | Bouchara Sa | Nouvelles quinolones fluorees, leur procede de preparation et les compositions pharmaceutiques en renfermant. |
TW252107B (es) * | 1993-08-27 | 1995-07-21 | Hokuriku Pharmacetical Co Ltd | |
ES2092963B1 (es) * | 1995-04-12 | 1997-12-16 | Sint Quimica Sa | Procedimiento para la preparacion del acido 1-ciclopropil-6-fluoro-1, 4-dihidro-7-(1s,4s)-5-metil-2,5-diazabiciclo(2.2.1) hept-2-il)-4-oxo-3-quinolincarboxilico y sus sales. |
SE0003795D0 (sv) | 2000-10-20 | 2000-10-20 | Astrazeneca Ab | Pharmaceutically useful compounds |
WO2011031745A1 (en) | 2009-09-09 | 2011-03-17 | Achaogen, Inc. | Antibacterial fluoroquinolone analogs |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1175836A (en) * | 1977-09-20 | 1984-10-09 | Marcel Pesson | Production of 1,4-dihydroquinoline-3-carboxylic acid derivatives |
DE2808070A1 (de) * | 1978-02-24 | 1979-08-30 | Bayer Ag | Verfahren zur herstellung von 4-pyridon-3-carbonsaeuren und/oder deren derivaten |
DE3267485D1 (en) * | 1981-02-18 | 1986-01-02 | Nippon Shinyaku Co Ltd | Substituted carboxylic acid derivatives |
US4499091A (en) * | 1982-03-31 | 1985-02-12 | Sterling Drug Inc. | 1-Amino (or substituted amino)-1,4-dihydro-4-oxo-6-fluoro-7-heterylquinoline-3-carboxylic acids and their use as antibacterial agents |
EP0090424B1 (en) * | 1982-03-31 | 1986-05-28 | Sterling Drug Inc. | New quinolone compounds and preparation thereof |
NZ208470A (en) * | 1983-07-18 | 1988-06-30 | Abbott Lab | 6-fluoro-1,4-dihydro-4-oxo-quinoline-3-carboxylic acid derivatives and antibacterial compositions containing such |
JPS6056959A (ja) * | 1983-07-18 | 1985-04-02 | アボツト ラボラトリ−ズ | キノリン抗菌性化合物 |
US4730000A (en) * | 1984-04-09 | 1988-03-08 | Abbott Laboratories | Quinoline antibacterial compounds |
US4571396A (en) * | 1984-04-16 | 1986-02-18 | Warner-Lambert Company | Antibacterial agents |
EP0181521A1 (en) * | 1984-10-19 | 1986-05-21 | Otsuka Pharmaceutical Co., Ltd. | Antimicrobial 1-substituted Phenyl-4-oxoquinoline-3-carboxylic acid compounds |
US4578473A (en) * | 1985-04-15 | 1986-03-25 | Warner-Lambert Company | Process for quinoline-3-carboxylic acid antibacterial agents |
IN166416B (es) * | 1985-09-18 | 1990-05-05 | Pfizer | |
DE3601567A1 (de) * | 1986-01-21 | 1987-07-23 | Bayer Ag | 7-(azabicycloalkyl)-chinoloncarbonsaeure- und -naphthyridon-carbonsaeure-derivate |
US4923879A (en) * | 1987-07-31 | 1990-05-08 | Warner-Lambert Company | 1,8-Naphthyridines and their use as antibacterial agents |
US4962108A (en) * | 1987-07-31 | 1990-10-09 | Warner-Lambert Company | Antibacterial quinoline compounds |
US4962112A (en) * | 1987-08-04 | 1990-10-09 | Abbott Laboratories | 7-(2-methyl-4-aminopyrrolidinyl)naphthryidine and quinoline compounds |
US4780468A (en) * | 1987-08-07 | 1988-10-25 | Warner-Lambert Company | 8-trifluoromethyl quinolones as antibacterial agents |
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 |
WO1989005643A1 (en) * | 1987-12-18 | 1989-06-29 | Pfizer Inc. | Heterocyclic-substituted quinoline-carboxylic acids |
US4920120A (en) * | 1988-01-25 | 1990-04-24 | Warner-Lambert Company | Antibacterial agents |
-
1987
- 1987-07-01 EP EP87109461A patent/EP0251308B1/de not_active Expired - Lifetime
- 1987-07-01 FI FI872897A patent/FI88506C/fi not_active IP Right Cessation
- 1987-07-01 AT AT87109461T patent/ATE58538T1/de not_active IP Right Cessation
- 1987-07-01 IL IL83049A patent/IL83049A/xx not_active IP Right Cessation
- 1987-07-01 DE DE8787109461T patent/DE3766299D1/de not_active Expired - Lifetime
- 1987-07-01 ES ES87109461T patent/ES2018667B3/es not_active Expired - Lifetime
- 1987-07-02 YU YU1246/87A patent/YU45039B/xx unknown
- 1987-07-02 NO NO872778A patent/NO166130C/no unknown
- 1987-07-03 PH PH35494A patent/PH24239A/en unknown
- 1987-07-03 PT PT85257A patent/PT85257B/pt not_active IP Right Cessation
- 1987-07-03 AR AR87308059A patent/AR245450A1/es active
- 1987-07-03 NZ NZ220950A patent/NZ220950A/xx unknown
- 1987-07-03 HU HU873023A patent/HU197907B/hu not_active IP Right Cessation
- 1987-07-03 ZA ZA874849A patent/ZA874849B/xx unknown
- 1987-07-03 AU AU75080/87A patent/AU608515B2/en not_active Ceased
- 1987-07-03 MY MYPI87000937A patent/MY101261A/en unknown
- 1987-07-03 CS CS875055A patent/CS277415B6/cs unknown
- 1987-07-03 JP JP62165560A patent/JPH07103123B2/ja not_active Expired - Lifetime
- 1987-07-03 SU SU874203001A patent/SU1551248A3/ru active
- 1987-07-03 DK DK342187A patent/DK342187A/da not_active Application Discontinuation
- 1987-07-04 KR KR1019870007133A patent/KR880001595A/ko not_active Application Discontinuation
- 1987-07-06 US US07/070,351 patent/US5045549A/en not_active Expired - Fee Related
- 1987-07-06 DD DD87304673A patent/DD262428A1/de not_active IP Right Cessation
-
1990
- 1990-11-23 GR GR90400603T patent/GR3001097T3/el unknown
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