ES2011919A6 - Metodo para producir compuestos antagonistas de los leucotrienos. - Google Patents
Metodo para producir compuestos antagonistas de los leucotrienos.Info
- Publication number
- ES2011919A6 ES2011919A6 ES8803652A ES8803652A ES2011919A6 ES 2011919 A6 ES2011919 A6 ES 2011919A6 ES 8803652 A ES8803652 A ES 8803652A ES 8803652 A ES8803652 A ES 8803652A ES 2011919 A6 ES2011919 A6 ES 2011919A6
- Authority
- ES
- Spain
- Prior art keywords
- stands
- carboxy
- bond
- stand
- alkyl
- 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
Links
- 229940111121 antirheumatic drug quinolines Drugs 0.000 title 1
- 150000003248 quinolines Chemical class 0.000 title 1
- 229910020008 S(O) Inorganic materials 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- -1 cyano, nitro, amino, carboxy Chemical group 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 150000002431 hydrogen Chemical class 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
- NEAQRZUHTPSBBM-UHFFFAOYSA-N 2-hydroxy-3,3-dimethyl-7-nitro-4h-isoquinolin-1-one Chemical compound C1=C([N+]([O-])=O)C=C2C(=O)N(O)C(C)(C)CC2=C1 NEAQRZUHTPSBBM-UHFFFAOYSA-N 0.000 abstract 1
- 239000000867 Lipoxygenase Inhibitor Substances 0.000 abstract 1
- 230000002378 acidificating effect Effects 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 239000003199 leukotriene receptor blocking agent Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000002577 pseudohalo group Chemical group 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical group OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic 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
- C07D215/12—Heterocyclic 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 substituted hydrocarbon radicals attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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
- C07D401/10—Heterocyclic 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 linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic 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
- C07D215/12—Heterocyclic 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 substituted hydrocarbon radicals attached to ring carbon atoms
- C07D215/14—Radicals substituted by oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Quinoline Compounds (AREA)
- Water Treatment By Sorption (AREA)
- Optical Transform (AREA)
- Ultra Sonic Daignosis Equipment (AREA)
- Optical Head (AREA)
- Luminescent Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
SEGUN ESTE METODO PARA PRODUCIR COMPUESTOS ANTAGONISTAS DE LOS LEUCOTRIENOS DE LA FORMULA (I) SE HACE REACCIONAR UNA AMINA DE FORMULA (II) CON UN COMPUESTO DE FORMULA (III) LA RELACION SE REALIZA EN UN DISOLVENTE ORGANICO INERTE, A UNA TEMPERATURA APROXIMADAMENTE AMBIENTAL O SUPERIOR HASTA EL PUNTO DE EBULLICION DEL DISOLVENTE. SE RECOGEN POR FILTRACION LOS PRODUCTOS CRUZADOS DE REACCION DE LA FORMULA (I), SI RESULTA CONVENIENTE DESPUES DE UNA DILUCION CON AGUA O SE EXTRAEN DE LA MEZCLA REACCIONAL. SE PURIFICAN LOS PRODUCTOS POR RECRISTALIZACION O POR CROMATOGRAFIA. ESTOS COMPUESTOS SON DE UTILIDAD EN MEDICINA Y VETERINARIA, COMO INHIBIDORES DE LA LIPOXIGENASA Y/O ANTAGONISTAS DE LOS LEUCOTRIENOS.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB878728051A GB8728051D0 (en) | 1987-12-01 | 1987-12-01 | Chemical compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2011919A6 true ES2011919A6 (es) | 1990-02-16 |
Family
ID=10627789
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES8803652A Expired - Lifetime ES2011919A6 (es) | 1987-12-01 | 1988-11-30 | Metodo para producir compuestos antagonistas de los leucotrienos. |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US5110819A (es) |
| EP (1) | EP0420844B1 (es) |
| JP (1) | JPH03501477A (es) |
| KR (1) | KR900700454A (es) |
| AT (1) | ATE110364T1 (es) |
| CA (1) | CA1336602C (es) |
| DE (1) | DE3851232T2 (es) |
| ES (1) | ES2011919A6 (es) |
| GB (1) | GB8728051D0 (es) |
| GR (1) | GR1000422B (es) |
| IE (1) | IE64473B1 (es) |
| NZ (1) | NZ227003A (es) |
| PH (1) | PH29985A (es) |
| PT (1) | PT89118B (es) |
| WO (1) | WO1989005294A1 (es) |
| ZA (1) | ZA888763B (es) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4920132A (en) * | 1987-11-03 | 1990-04-24 | Rorer Pharmaceutical Corp. | Quinoline derivatives and use thereof as antagonists of leukotriene D4 |
| GB8919504D0 (en) * | 1989-08-29 | 1989-10-11 | Leo Pharm Prod Ltd | Chemical compounds |
| US5021576A (en) * | 1989-10-27 | 1991-06-04 | American Home Products Corporation | 2-Anilino phenylacetic acid derivatives |
| AU654140B2 (en) * | 1990-07-31 | 1994-10-27 | Lilly Industries Limited | N-benzyl indoles, processes for their preparation or pharmaceutical compositions containing them |
| US5281593A (en) * | 1990-07-31 | 1994-01-25 | Lilly Industries Limited | Certain indole derivatives useful as leukotriene antagonists |
| WO1994014797A1 (en) * | 1992-12-23 | 1994-07-07 | Smithkline Beecham Corporation | Quinoline compounds and the treatment of leucotriene related diseases therewith |
| US5486612A (en) * | 1993-12-14 | 1996-01-23 | Eli Lilly And Company | N-benzyl dihydroindole LTD4 antagonists |
| GB9414590D0 (en) * | 1994-07-20 | 1994-09-07 | Leo Pharm Prod Ltd | Chemical compounds |
| ES2103180B1 (es) * | 1994-08-01 | 1998-04-01 | Menarini Lab | Fenilacetamidas con accion antagonista de los leucotrienos. |
| US5602110A (en) * | 1994-08-31 | 1997-02-11 | Case Western Reserve University | Method and composition for treating cystic fibrosis |
| EP0725063A1 (de) * | 1995-02-01 | 1996-08-07 | Ciba-Geigy Ag | Chinolin-Derivate |
| ES2117551B1 (es) * | 1995-12-29 | 1999-04-01 | Menarini Lab | Quinolinas naftalenicas con accion antagonista de los leucotrienos, procedimiento para su preparacion y utilizacion de las mismas. |
| US5756518A (en) * | 1996-04-02 | 1998-05-26 | Kowa Co., Ltd. | Phenylene derivatives |
| US6255321B1 (en) | 1997-06-17 | 2001-07-03 | Kaken Pharmaceutical Co., Ltd. | 2-sulfamoylbenzoic acid derivatives |
| JP2004137284A (ja) * | 1997-06-17 | 2004-05-13 | Kaken Pharmaceut Co Ltd | 2−スルファモイル安息香酸誘導体 |
| US6376671B1 (en) | 1997-06-17 | 2002-04-23 | Kaken Pharmaceutical Co., Ltd. | 2-sulfamoylbenzoic acid derivatives |
| ES2176877T3 (es) * | 1997-09-26 | 2002-12-01 | Kowa Co | Derivados de tetrazol como antagonistas de ltd4 y h1. |
| PT1177176E (pt) | 1999-04-28 | 2006-08-31 | Aventis Pharma Gmbh | Derivados de acidos triarilicos como ligandos de receptores ppar. |
| IL151517A0 (en) * | 2000-03-09 | 2003-04-10 | Aventis Pharma Gmbh | Therapeutic uses of ppar mediators |
| TW200418825A (en) | 2002-12-16 | 2004-10-01 | Hoffmann La Roche | Novel (R)-and (S) enantiomers of thiophene hydroxamic acid derivatives |
| WO2005087710A1 (ja) * | 2004-03-15 | 2005-09-22 | Takeda Pharmaceutical Company Limited | アミノフェニルプロパン酸誘導体 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4625034A (en) * | 1985-02-04 | 1986-11-25 | Usv Pharmaceutical Corp. | 1,2-Dihydro; 1,2,3,4-tetrahydro; 5,8 dihydro; and 5,6,7,8-tetrahydroquinoline derivatives |
| IE58870B1 (en) * | 1985-03-08 | 1993-11-17 | Leo Pharm Prod Ltd | Pyridine derivatives |
| US4839369A (en) * | 1985-04-16 | 1989-06-13 | Rorer Pharmaceutical Corporation | Aryl and heteroaryl ethers as agents for the treatment of hypersensitive ailments |
| DK282986A (da) * | 1985-06-18 | 1987-02-24 | Merck Frosst Canada Inc | Substitueret quinolin og farmaceutisk praeparat indeholdende en saadan forbindelse |
| EP0219307A3 (en) * | 1985-10-16 | 1987-10-14 | Merck Frosst Canada Inc. | 2-substituted quinolines |
| DE3682160D1 (de) * | 1985-10-16 | 1991-11-28 | Merck Frosst Canada Inc | 2-substituierte chinoline. |
| GB2185741B (en) * | 1986-01-27 | 1989-10-25 | American Home Prod | Heterocyclic sulphonamides |
| US4904786A (en) * | 1986-01-27 | 1990-02-27 | American Home Products Corporation | Quinoline compounds as antiallergic and antiinflammatory agents |
| IE59889B1 (en) * | 1986-02-14 | 1994-04-20 | Merck Frosst Canada Inc | 2-substituted quinoline dioic acids |
| EP0271287A3 (en) * | 1986-12-11 | 1990-06-13 | Merck Frosst Canada Inc. | Quinoline dioic acids and amides |
| US4920132A (en) * | 1987-11-03 | 1990-04-24 | Rorer Pharmaceutical Corp. | Quinoline derivatives and use thereof as antagonists of leukotriene D4 |
| DE3814504A1 (de) * | 1988-04-29 | 1989-11-09 | Bayer Ag | (alpha)-substituierte 4-(chinolin-2-yl-methoxy)phenylessigsaeuren und -ester, verfahren zu ihrer herstellung und ihre verwendung in arzneimitteln |
-
1987
- 1987-12-01 GB GB878728051A patent/GB8728051D0/en active Pending
-
1988
- 1988-11-15 IE IE341988A patent/IE64473B1/en not_active IP Right Cessation
- 1988-11-17 US US07/476,403 patent/US5110819A/en not_active Expired - Fee Related
- 1988-11-17 WO PCT/DK1988/000188 patent/WO1989005294A1/en not_active Ceased
- 1988-11-17 AT AT89900021T patent/ATE110364T1/de not_active IP Right Cessation
- 1988-11-17 DE DE3851232T patent/DE3851232T2/de not_active Expired - Fee Related
- 1988-11-17 JP JP1500028A patent/JPH03501477A/ja active Pending
- 1988-11-17 EP EP89900021A patent/EP0420844B1/en not_active Expired - Lifetime
- 1988-11-18 NZ NZ227003A patent/NZ227003A/xx unknown
- 1988-11-23 ZA ZA888763A patent/ZA888763B/xx unknown
- 1988-11-25 PH PH37861A patent/PH29985A/en unknown
- 1988-11-25 GR GR880100797A patent/GR1000422B/el unknown
- 1988-11-28 CA CA000584360A patent/CA1336602C/en not_active Expired - Fee Related
- 1988-11-30 PT PT89118A patent/PT89118B/pt not_active IP Right Cessation
- 1988-11-30 ES ES8803652A patent/ES2011919A6/es not_active Expired - Lifetime
-
1989
- 1989-07-22 KR KR1019890701385A patent/KR900700454A/ko not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| EP0420844B1 (en) | 1994-08-24 |
| US5110819A (en) | 1992-05-05 |
| JPH03501477A (ja) | 1991-04-04 |
| CA1336602C (en) | 1995-08-08 |
| ZA888763B (en) | 1989-07-26 |
| EP0420844A1 (en) | 1991-04-10 |
| DE3851232D1 (de) | 1994-09-29 |
| GR1000422B (el) | 1992-06-30 |
| KR900700454A (ko) | 1990-08-13 |
| PT89118A (pt) | 1988-12-01 |
| IE883419L (en) | 1989-06-01 |
| ATE110364T1 (de) | 1994-09-15 |
| PH29985A (en) | 1996-10-29 |
| IE64473B1 (en) | 1995-08-09 |
| DE3851232T2 (de) | 1995-02-02 |
| GB8728051D0 (en) | 1988-01-06 |
| NZ227003A (en) | 1991-11-26 |
| PT89118B (pt) | 1993-04-30 |
| WO1989005294A1 (en) | 1989-06-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| SA6 | Expiration date (snapshot 920101) |
Free format text: 2008-11-30 |
|
| FD1A | Patent lapsed |
Effective date: 20010301 |