BG49275A3 - Метод за получаване на заместени диазабицикло алкилхинолин карбонови киселини - Google Patents
Метод за получаване на заместени диазабицикло алкилхинолин карбонови киселиниInfo
- Publication number
- BG49275A3 BG49275A3 BG076465A BG7646586A BG49275A3 BG 49275 A3 BG49275 A3 BG 49275A3 BG 076465 A BG076465 A BG 076465A BG 7646586 A BG7646586 A BG 7646586A BG 49275 A3 BG49275 A3 BG 49275A3
- Authority
- BG
- Bulgaria
- Prior art keywords
- general formula
- alkyl
- carbon
- attached
- diazobicycloalkylchinolin
- 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.)
- Active
Links
- 150000004649 carbonic acid derivatives Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 1
- 230000000844 anti-bacterial effect Effects 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 239000003899 bactericide agent Substances 0.000 abstract 1
- 150000001768 cations Chemical class 0.000 abstract 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 abstract 1
- -1 n-methylamino, p-fluorophenyl Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- LOAUVZALPPNFOQ-UHFFFAOYSA-N quinaldic acid Chemical class C1=CC=CC2=NC(C(=O)O)=CC=C21 LOAUVZALPPNFOQ-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 abstract 1
Classifications
-
- 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
- C07D471/08—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
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Communicable Diseases (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Saccharide Compounds (AREA)
- Materials For Photolithography (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Методът намира приложение във фармацевтичната промишленост за получаване на бактерицидни средства с висока антибактериална ективност. Съединенията имат обща формула в която r1 означава водород, фармацевтично приемлив катион или /с1-с6/ алкил; а означава сн или сf; у означава /с1-с3/ алкил, /с1-с3/ халогеналкил, циклопропил, винил, n-метиламино, р-флуорфенил; а въглерод и, взет заедно с у и въглерода и азота, към които а и у са прикрепени, образува 6-членен пръстен, който може да съдържа кислород и към който може да бъде прикрепен r3, означаващ метил или метилен, а r2 означава диазабициклоалкил с вътрешен мост. Методът се състои във взаимодействие на съответно заместена с халоген хинолинкарбонова киселина със съединение с обща формула r2н, в която r2 има значенията, посочени по-горе, и незадължително превръщане на полученото съединение с обща формула i в присъединителна с киселина сол. 3 претенции
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US77747185A | 1985-09-18 | 1985-09-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
BG49275A3 true BG49275A3 (bg) | 1991-09-16 |
Family
ID=25110350
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BG076465A Active BG49275A3 (bg) | 1985-09-18 | 1986-09-18 | Метод за получаване на заместени диазабицикло алкилхинолин карбонови киселини |
BG096080A BG61091B2 (bg) | 1985-09-18 | 1992-03-17 | Антибактериални заместени мостови-диазабициклоалкил хинолон карбоксилови киселини |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BG096080A BG61091B2 (bg) | 1985-09-18 | 1992-03-17 | Антибактериални заместени мостови-диазабициклоалкил хинолон карбоксилови киселини |
Country Status (42)
Country | Link |
---|---|
US (3) | US4775668A (bg) |
EP (1) | EP0215650B1 (bg) |
JP (1) | JPH0798819B2 (bg) |
KR (1) | KR870000961B1 (bg) |
CN (1) | CN1014789B (bg) |
AT (1) | ATE72245T1 (bg) |
AU (1) | AU576302B2 (bg) |
BG (2) | BG49275A3 (bg) |
CA (1) | CA1340734C (bg) |
CY (1) | CY1774A (bg) |
CZ (1) | CZ277825B6 (bg) |
DD (1) | DD259190A5 (bg) |
DE (2) | DE3683711D1 (bg) |
DK (1) | DK171276B1 (bg) |
EG (1) | EG18184A (bg) |
ES (1) | ES2001428A6 (bg) |
FI (1) | FI87565C (bg) |
GR (1) | GR862363B (bg) |
HK (1) | HK132795A (bg) |
HU (1) | HU200462B (bg) |
IE (1) | IE58966B1 (bg) |
IL (1) | IL80033A (bg) |
IN (1) | IN166416B (bg) |
LU (1) | LU90356I2 (bg) |
MA (1) | MA20770A1 (bg) |
MW (1) | MW5886A1 (bg) |
MX (1) | MX173358B (bg) |
MY (1) | MY102518A (bg) |
NO (1) | NO170335C (bg) |
NZ (1) | NZ217614A (bg) |
OA (1) | OA08410A (bg) |
PH (2) | PH24048A (bg) |
PL (1) | PL149987B1 (bg) |
PT (1) | PT83388B (bg) |
SG (1) | SG28094G (bg) |
SK (1) | SK667886A3 (bg) |
SU (1) | SU1482531A3 (bg) |
UA (1) | UA6340A1 (bg) |
YU (1) | YU45024B (bg) |
ZA (1) | ZA867063B (bg) |
ZM (1) | ZM8586A1 (bg) |
ZW (1) | ZW19386A1 (bg) |
Families Citing this family (59)
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IN166416B (bg) * | 1985-09-18 | 1990-05-05 | Pfizer | |
DE3601567A1 (de) * | 1986-01-21 | 1987-07-23 | Bayer Ag | 7-(azabicycloalkyl)-chinoloncarbonsaeure- und -naphthyridon-carbonsaeure-derivate |
ES2018667B3 (es) * | 1986-07-04 | 1991-05-01 | Chemie Linz Gmbh | Derivados del acido 4-qionolon-3-carboxilico, procedimiento para su obtencion y preparados farmaceuticos que los contienen. |
US4965273A (en) * | 1986-10-08 | 1990-10-23 | Bristol-Myers Company | Certain 1-tertiary-butyl-naphthyridone carboxylic acid derivatives anti-bacterial agents |
WO1989000158A1 (en) * | 1987-07-02 | 1989-01-12 | Pfizer Inc. | Bridged-diazabicycloalkyl quinolone carboxylic acids and esters |
US4923879A (en) * | 1987-07-31 | 1990-05-08 | Warner-Lambert Company | 1,8-Naphthyridines and their use as antibacterial agents |
US4968799A (en) * | 1987-07-31 | 1990-11-06 | Warner-Lambert Company | Antibacterial agents |
US4992546A (en) * | 1987-07-31 | 1991-02-12 | Warner-Lambert Company | Process for preparing 6,8-diazabicyclo[3.2.2]nonane derivatives |
US4933335A (en) * | 1987-08-07 | 1990-06-12 | Warner-Lambert Company | Quinolones as antibacterial agents |
WO1989005643A1 (en) * | 1987-12-18 | 1989-06-29 | Pfizer Inc. | Heterocyclic-substituted quinoline-carboxylic acids |
DE3902079A1 (de) * | 1988-04-15 | 1989-10-26 | Bayer Ag | I.m. injektionsformen von gyrase-inhibitoren |
WO1990002123A1 (en) * | 1988-08-23 | 1990-03-08 | Pfizer Inc. | Amino-substituted bridged azabicyclic quinolone carboxylic acids and esters |
US5147873A (en) * | 1988-08-23 | 1992-09-15 | Pfizer Inc. | Amino-substituted bridged azabicyclic quinolone carboxylic acids and esters |
US4895943A (en) * | 1988-10-25 | 1990-01-23 | Pfizer Inc. | Preparation of 1,4-diazabicyclo(3.2.2)nonane |
US5036153A (en) * | 1989-05-11 | 1991-07-30 | Braish Tamim F | Preparation of 2,5-diazabicyclo[2.2.1]heptanes and intermediates |
US5214051A (en) * | 1989-08-01 | 1993-05-25 | Pfizer Inc. | Thiazolyl and oxazolyl[5,4-c]piperidyl-substituted quinolone-carboxylic acid and related analogs thereof having antibacterial properties are disclosed |
US5157125A (en) * | 1989-09-25 | 1992-10-20 | Pfizer Inc. | Optically active 2-alkyl-2,5-diazabicyclo[2.2.1]heptanes |
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US6056436A (en) * | 1997-02-20 | 2000-05-02 | University Of Maryland | Simultaneous measurement of temperature and strain using optical sensors |
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IN166416B (bg) * | 1985-09-18 | 1990-05-05 | Pfizer | |
US4772706A (en) * | 1986-01-13 | 1988-09-20 | Warner-Lambert Company | Process for quinoline-3-carboxylic acid antibacterial agents |
US4840956A (en) * | 1986-02-18 | 1989-06-20 | Warner-Lambert Company | Novel disubstituted-7-pyrrolidinoquinoline antibacterial agents |
ES2018667B3 (es) * | 1986-07-04 | 1991-05-01 | Chemie Linz Gmbh | Derivados del acido 4-qionolon-3-carboxilico, procedimiento para su obtencion y preparados farmaceuticos que los contienen. |
DE3721745A1 (de) * | 1986-07-04 | 1988-01-14 | Lentia Gmbh | Bicyclisch substituierte chinoloncarbonsaeurederivate, verfahren zu ihrer herstellung und diese enthaltende pharmazeutische praeparate |
DE3641312A1 (de) * | 1986-12-03 | 1988-06-09 | Bayer Ag | Verfahren zur herstellung von chinolincarbonsaeuren |
US4923879A (en) * | 1987-07-31 | 1990-05-08 | Warner-Lambert Company | 1,8-Naphthyridines and their use 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 |
-
1986
- 1986-08-18 IN IN740/DEL/86A patent/IN166416B/en unknown
- 1986-08-19 US US06/898,458 patent/US4775668A/en not_active Expired - Lifetime
- 1986-08-19 US US06/898,473 patent/US4861779A/en not_active Expired - Lifetime
- 1986-08-28 MW MW58/86A patent/MW5886A1/xx unknown
- 1986-09-03 ZM ZM85/86A patent/ZM8586A1/xx unknown
- 1986-09-12 AT AT86307045T patent/ATE72245T1/de active
- 1986-09-12 EP EP86307045A patent/EP0215650B1/en not_active Expired - Lifetime
- 1986-09-12 DE DE8686307045T patent/DE3683711D1/de not_active Expired - Lifetime
- 1986-09-12 DE DE1996175019 patent/DE19675019I2/de active Active
- 1986-09-15 IL IL80033A patent/IL80033A/xx not_active IP Right Cessation
- 1986-09-15 EG EG580/86A patent/EG18184A/xx active
- 1986-09-16 GR GR862363A patent/GR862363B/el unknown
- 1986-09-16 SK SK6678-86A patent/SK667886A3/sk unknown
- 1986-09-16 CA CA000518238A patent/CA1340734C/en not_active Expired - Lifetime
- 1986-09-16 ES ES8601935A patent/ES2001428A6/es not_active Expired
- 1986-09-16 PT PT83388A patent/PT83388B/pt unknown
- 1986-09-16 PL PL1986261410A patent/PL149987B1/pl unknown
- 1986-09-16 CZ CS866678A patent/CZ277825B6/cs not_active IP Right Cessation
- 1986-09-17 OA OA58953A patent/OA08410A/xx unknown
- 1986-09-17 DD DD86294486A patent/DD259190A5/de unknown
- 1986-09-17 SU SU864028142A patent/SU1482531A3/ru active
- 1986-09-17 KR KR1019860007855A patent/KR870000961B1/ko not_active IP Right Cessation
- 1986-09-17 AU AU62768/86A patent/AU576302B2/en not_active Expired
- 1986-09-17 CN CN86106385A patent/CN1014789B/zh not_active Expired
- 1986-09-17 IE IE247986A patent/IE58966B1/en not_active IP Right Cessation
- 1986-09-17 FI FI863756A patent/FI87565C/fi not_active IP Right Cessation
- 1986-09-17 NZ NZ217614A patent/NZ217614A/xx unknown
- 1986-09-17 NO NO863718A patent/NO170335C/no not_active IP Right Cessation
- 1986-09-17 UA UA4028142A patent/UA6340A1/uk unknown
- 1986-09-17 ZW ZW193/86A patent/ZW19386A1/xx unknown
- 1986-09-17 MX MX003751A patent/MX173358B/es unknown
- 1986-09-17 YU YU1617/86A patent/YU45024B/xx unknown
- 1986-09-17 HU HU863976A patent/HU200462B/hu unknown
- 1986-09-17 ZA ZA867063A patent/ZA867063B/xx unknown
- 1986-09-17 DK DK445886A patent/DK171276B1/da not_active IP Right Cessation
- 1986-09-17 MA MA20998A patent/MA20770A1/fr unknown
- 1986-09-18 JP JP61220819A patent/JPH0798819B2/ja not_active Expired - Lifetime
- 1986-09-18 BG BG076465A patent/BG49275A3/bg active Active
- 1986-09-18 PH PH34266A patent/PH24048A/en unknown
-
1987
- 1987-08-25 MY MYPI87001447A patent/MY102518A/en unknown
-
1988
- 1988-02-16 US US07/157,182 patent/US5091383A/en not_active Expired - Fee Related
-
1989
- 1989-07-11 PH PH38922A patent/PH25338A/en unknown
-
1992
- 1992-03-17 BG BG096080A patent/BG61091B2/bg unknown
-
1994
- 1994-02-22 SG SG28094A patent/SG28094G/en unknown
-
1995
- 1995-08-24 HK HK132795A patent/HK132795A/xx not_active IP Right Cessation
- 1995-10-20 CY CY177495A patent/CY1774A/xx unknown
-
1999
- 1999-02-24 LU LU90356C patent/LU90356I2/xx unknown
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