AR006271A1 - Derivados de imidazol [2,1-b][3] benzacepina, un procedimiento para su preparacion, una composicion farmaceutica que los contiene, un procedimientopara preparar dicha composicion farmaceutica - Google Patents
Derivados de imidazol [2,1-b][3] benzacepina, un procedimiento para su preparacion, una composicion farmaceutica que los contiene, un procedimientopara preparar dicha composicion farmaceuticaInfo
- Publication number
- AR006271A1 AR006271A1 ARP970101072A ARP970101072A AR006271A1 AR 006271 A1 AR006271 A1 AR 006271A1 AR P970101072 A ARP970101072 A AR P970101072A AR P970101072 A ARP970101072 A AR P970101072A AR 006271 A1 AR006271 A1 AR 006271A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- hydrogen
- pharmaceutical composition
- alkyloxy
- procedure
- Prior art date
Links
Classifications
-
- 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
- C07D487/12—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 three hetero rings
- C07D487/14—Ortho-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
-
- 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
-
- 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
- A61P31/06—Antibacterial agents for tuberculosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
- A61P33/04—Amoebicides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
- A61P33/06—Antimalarials
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- C07D471/04—Ortho-condensed systems
-
- 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
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D495/14—Ortho-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Tropical Medicine & Parasitology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Hematology (AREA)
- Pulmonology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Se relaciona con derivados de imidazol[2,1-b][3]benzacepina de la fórmula (I). Las formas de N-óxido, las sales de adición farmacéuticamente aceptablesy las formas estereoquímicamente isoméricas de los mismos, en los cuales la línea de puntose s un enlace optativo; n es 1 o 2; R1 es hidrógeno, halo,formilo, alquilo C1-4, alquilo C1-4 sustituido con hidroxi alquiloxi C1-4, alquilcarboniloxi C1-4, imidazolilo, tiazolilo u oxazolilo, o un radical dela fórmula: -X-CO-OR5, -X-CO-NR6R7,o - X-COR10, en la cual -X- es un enlace directo, alcandiilo C1-4,o alquendiilo C2-6; R5 es hidrógeno, alquilo C1-12;Ar, Het, alquilo C1-C6 sustituido con alquiloxi C1-4 arilo o heteroarilo; cada uno de R6 y R7 independientemente eshidrógeno o alquilo C1-C4; R2 eshidrógeno, halo, alquilo C1-C4, hidroxialquilo C1-4, alquiloxicarboniloC1-4, carboxilo, formilo o fenilo; R3 es hidrógeno, alquilo C1-C4 o alquiloxiC1-4; R4 es hidrógeno, halo, alquilo C1-C4, alquiloxi C1-4 o haloc1-4alquilo; Z es -CH2, CH2-CH2- o -CH=CH-, -CHOH-CH2-,-O-CH2-,-C(=O)-CH2, o -C(=NOH-CH2;-A-B- es un radical bivalente; -A1- es un enlace directo, alcandiilo C1-6, optativamente sustituido, C1-6alcandiil-oxi C1-6 acandiilo, alcandiiloxiC1-6,carbonil, alca ndiilcarbonilo C1-6, alcandiiloxi C1-6 optativamente sustituido, -A2- es un enlace directo o alcandiilo C1-6; y Q es arilo. Se describenprocesos para preparar dichos productos, una composición farmacéutica que comprendelos mismos, un procedim iento para preparar dicha composiciónfarmacéutica, un producto y el uso de dichos compuestos como medicamento para inhibir o revertir los efectos de la resistencia a los fármacos múltiples.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP96200755 | 1996-03-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR006271A1 true AR006271A1 (es) | 1999-08-11 |
Family
ID=8223797
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP970101072A AR006271A1 (es) | 1996-03-19 | 1997-03-18 | Derivados de imidazol [2,1-b][3] benzacepina, un procedimiento para su preparacion, una composicion farmaceutica que los contiene, un procedimientopara preparar dicha composicion farmaceutica |
Country Status (29)
| Country | Link |
|---|---|
| US (3) | US6218381B1 (es) |
| EP (1) | EP0888352B1 (es) |
| JP (3) | JP3630434B2 (es) |
| KR (2) | KR100349500B1 (es) |
| CN (1) | CN1083453C (es) |
| AR (1) | AR006271A1 (es) |
| AT (1) | ATE241626T1 (es) |
| BG (1) | BG62734B1 (es) |
| BR (1) | BR9708140A (es) |
| CA (1) | CA2237594C (es) |
| CZ (1) | CZ294060B6 (es) |
| DE (1) | DE69722389T2 (es) |
| EA (1) | EA001004B1 (es) |
| EE (1) | EE03773B1 (es) |
| ES (1) | ES2200159T3 (es) |
| HR (1) | HRP970161B1 (es) |
| HU (1) | HU224528B1 (es) |
| ID (1) | ID16375A (es) |
| IL (1) | IL124572A (es) |
| MX (1) | MX9804426A (es) |
| MY (1) | MY118282A (es) |
| NO (1) | NO310659B1 (es) |
| NZ (1) | NZ330466A (es) |
| PL (1) | PL193444B1 (es) |
| SK (1) | SK284434B6 (es) |
| TR (1) | TR199801191T2 (es) |
| TW (1) | TW527186B (es) |
| WO (1) | WO1997034897A1 (es) |
| ZA (1) | ZA972351B (es) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3775780B2 (ja) * | 1997-09-18 | 2006-05-17 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | 薬剤の経口的バイオアベイラビリテイを向上させるための縮合イミダゾール誘導体 |
| KR100661879B1 (ko) * | 1998-04-01 | 2006-12-27 | 스키에파마 캐나다 인코포레이티드 | 항암 조성물 |
| US6743794B2 (en) | 1999-12-22 | 2004-06-01 | Eli Lilly And Company | Methods and compounds for inhibiting MRP1 |
| US6376514B1 (en) | 2000-10-17 | 2002-04-23 | The Procter & Gamble Co. | Substituted six-membered heterocyclic compounds useful for treating multidrug resistance and compositions and methods thereof |
| US6693099B2 (en) | 2000-10-17 | 2004-02-17 | The Procter & Gamble Company | Substituted piperazine compounds optionally containing a quinolyl moiety for treating multidrug resistance |
| JP4452496B2 (ja) | 2001-06-12 | 2010-04-21 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | 新規な置換四環式イミダゾール誘導体、それらの製造法、それらを含む製薬学的組成物及び薬剤としてのそれらの使用 |
| AU2002356715B2 (en) * | 2001-11-23 | 2008-05-15 | Janssen Pharmaceutica N.V. | The use of anti-histaminics for acute reduction of elevated intracranial pressure |
| GB0301736D0 (en) * | 2003-01-24 | 2003-02-26 | Xenova Ltd | Pharmaceutical compounds |
| WO2014154620A1 (en) * | 2013-03-25 | 2014-10-02 | Crystal Pharma S.A.U. | Methods for the preparation of alcaftadine |
| CN103408549B (zh) * | 2013-06-14 | 2016-01-20 | 苏州汇和药业有限公司 | 一种阿卡他定中间体的制备方法 |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2418502C3 (de) * | 1974-04-11 | 1980-04-24 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | Dichlorbenzyl- [2-( a -imidazolylbutyl)-phenyl] -äther und -thioäther, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Arzneimittel |
| US4153719A (en) * | 1977-09-06 | 1979-05-08 | Sterling Drug Inc. | Aromatic diketones |
| JPS56125326A (en) * | 1980-03-07 | 1981-10-01 | Asahi Kagaku Kogyo Kk | Preparation of chlorinated phenoxytoluenes in high selectivity |
| US4778931A (en) | 1982-12-01 | 1988-10-18 | Usv Pharmaceutical Corporation | Certain [3-(1-hydroxy hexyl-tetrahydro)naphthalenes], the corresponding naphthalenes having anti-inflammatory and anti-allergic activity |
| US4794188A (en) | 1982-12-01 | 1988-12-27 | Usv Pharmaceutical Corporation | Certain unsymmetrical quinolinyl ethers having anti-inflammatory and anti-allergic activity |
| US4567184A (en) | 1982-12-01 | 1986-01-28 | Usv Pharmaceutical Corporation | Certain aryl or hetero-aryl derivatives of 1-hydroxy-pentane or 1-hydroxy-hexane which are useful for treating inflammation and allergies |
| US4588722A (en) | 1984-01-09 | 1986-05-13 | Janssen Pharmaceutica N.V. | N-(4-piperidinyl) bicyclic condensed 2-imidazolamine derivatives |
| JPS61151176A (ja) * | 1984-12-24 | 1986-07-09 | Sumitomo Chem Co Ltd | ベンズイミダゾール誘導体およびそれを有効成分とする殺虫、殺ダニ剤 |
| US4631287A (en) * | 1985-04-16 | 1986-12-23 | Usv Pharmaceutical Corp. | Aryl and heteroaryl ethers as agents for the treatment of hypersensitive ailments |
| AU7100887A (en) * | 1986-04-07 | 1987-10-08 | Sumitomo Chemical Company, Limited | Halogenated aromatic ethers and alcohol and aldehyde intermediates |
| JPS6475441A (en) * | 1987-09-16 | 1989-03-22 | Sumitomo Chemical Co | Production of optically active ether compound |
| JPH01254680A (ja) * | 1988-04-01 | 1989-10-11 | Sumitomo Chem Co Ltd | 複素環化合物、その製造法およびそれを有効成分とする殺菌剤 |
| JPH089616B2 (ja) * | 1990-10-10 | 1996-01-31 | シェリング・コーポレーション | 置換されたイミダゾベンズアゼピン類およびイミダゾピリドアゼピン類 |
| IL101850A (en) | 1991-06-13 | 1996-01-31 | Janssen Pharmaceutica Nv | 11-(4-Piperidinyl)-imidazo (2,1-b) (3) benzazepine derivatives their preparation and pharmaceutical compositions containing them |
| IL101851A (en) | 1991-06-13 | 1996-05-14 | Janssen Pharmaceutica Nv | 10-(4-piperidinyl- and piperidinylidene)-imidazo [1,2-a] (pyrrolo thieno or furano) [2,3] azepine derivatives their preparation and pharmaceutical compositions containing them and certain novel intermediates therefor |
| GB9122590D0 (en) * | 1991-10-24 | 1991-12-04 | Lilly Industries Ltd | Pharmaceutical compounds |
| AU662602B2 (en) | 1992-02-06 | 1995-09-07 | Merrell Dow Pharmaceuticals Inc. | Reversal of multi-drug resistance by triphenyl-azacycloalkane derivatives |
| KR100251295B1 (ko) | 1992-12-04 | 2000-05-01 | 디르크 반테 | 항앨러지성 이미다조[1,2-a](피롤로, 티에노 또는 푸라노)[2,3-d]아제핀 유도체(Antiallergic imidazo[1,2-a](pyrrolo, thieno or furano)[2,3-d]azepine derivatives) |
| WO1994022842A1 (en) | 1993-03-29 | 1994-10-13 | Basf Aktiengesellschaft | 1-amino-3-phenoxy propane derivatives as modulators of multi-drug resistance |
| EP0708776B1 (en) | 1993-07-13 | 2001-01-03 | Janssen Pharmaceutica N.V. | Antiallergic imidazoazepines |
| US5486612A (en) * | 1993-12-14 | 1996-01-23 | Eli Lilly And Company | N-benzyl dihydroindole LTD4 antagonists |
| US5596008A (en) * | 1995-02-10 | 1997-01-21 | G. D. Searle & Co. | 3,4-Diaryl substituted pyridines for the treatment of inflammation |
| FR2731708B1 (fr) | 1995-03-13 | 1997-04-30 | Synthelabo | Derives de piperidine, leur procede de preparation et leur application en therapeutique |
| TW382017B (en) | 1995-12-27 | 2000-02-11 | Janssen Pharmaceutica Nv | 1-(1,2-disubstituted piperidinyl)-4-(fused imidazole)-piperidine derivatives |
-
1997
- 1997-03-05 TW TW086102623A patent/TW527186B/zh not_active IP Right Cessation
- 1997-03-11 SK SK662-98A patent/SK284434B6/sk not_active IP Right Cessation
- 1997-03-11 EA EA199800586A patent/EA001004B1/ru unknown
- 1997-03-11 TR TR1998/01191T patent/TR199801191T2/xx unknown
- 1997-03-11 KR KR1020017008287A patent/KR100349500B1/ko not_active Expired - Fee Related
- 1997-03-11 HU HU9900415A patent/HU224528B1/hu not_active IP Right Cessation
- 1997-03-11 US US09/142,932 patent/US6218381B1/en not_active Expired - Fee Related
- 1997-03-11 AT AT97908226T patent/ATE241626T1/de not_active IP Right Cessation
- 1997-03-11 KR KR1019980703754A patent/KR100330698B1/ko not_active Expired - Fee Related
- 1997-03-11 EP EP97908226A patent/EP0888352B1/en not_active Expired - Lifetime
- 1997-03-11 CA CA002237594A patent/CA2237594C/en not_active Expired - Fee Related
- 1997-03-11 PL PL97327985A patent/PL193444B1/pl not_active IP Right Cessation
- 1997-03-11 NZ NZ330466A patent/NZ330466A/xx unknown
- 1997-03-11 IL IL12457297A patent/IL124572A/en not_active IP Right Cessation
- 1997-03-11 BR BR9708140A patent/BR9708140A/pt not_active IP Right Cessation
- 1997-03-11 ES ES97908226T patent/ES2200159T3/es not_active Expired - Lifetime
- 1997-03-11 CN CN97192399A patent/CN1083453C/zh not_active Expired - Fee Related
- 1997-03-11 CZ CZ19981529A patent/CZ294060B6/cs not_active IP Right Cessation
- 1997-03-11 DE DE69722389T patent/DE69722389T2/de not_active Expired - Fee Related
- 1997-03-11 EE EE9800281A patent/EE03773B1/xx not_active IP Right Cessation
- 1997-03-11 WO PCT/EP1997/001264 patent/WO1997034897A1/en not_active Ceased
- 1997-03-11 JP JP53312197A patent/JP3630434B2/ja not_active Expired - Fee Related
- 1997-03-17 MY MYPI97001123A patent/MY118282A/en unknown
- 1997-03-18 ZA ZA972351A patent/ZA972351B/xx unknown
- 1997-03-18 AR ARP970101072A patent/AR006271A1/es unknown
- 1997-03-19 HR HR970161A patent/HRP970161B1/xx not_active IP Right Cessation
- 1997-03-19 ID IDP970888A patent/ID16375A/id unknown
-
1998
- 1998-05-11 NO NO19982124A patent/NO310659B1/no not_active IP Right Cessation
- 1998-05-18 BG BG102459A patent/BG62734B1/bg unknown
- 1998-06-03 MX MX9804426A patent/MX9804426A/es not_active IP Right Cessation
-
2001
- 2001-02-02 US US09/775,524 patent/US6476018B1/en not_active Expired - Fee Related
- 2001-06-01 JP JP2001167003A patent/JP4205319B2/ja not_active Expired - Fee Related
-
2002
- 2002-07-02 US US10/187,665 patent/US20030087895A1/en not_active Abandoned
-
2003
- 2003-10-08 JP JP2003349802A patent/JP4251447B2/ja not_active Expired - Fee Related
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Legal Events
| Date | Code | Title | Description |
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| FB | Suspension of granting procedure |