HK68996A - Dibenz [b,e] oxepin derivative and antiallergic and antiinflammatory agent - Google Patents
Dibenz [b,e] oxepin derivative and antiallergic and antiinflammatory agent Download PDFInfo
- Publication number
- HK68996A HK68996A HK68996A HK68996A HK68996A HK 68996 A HK68996 A HK 68996A HK 68996 A HK68996 A HK 68996A HK 68996 A HK68996 A HK 68996A HK 68996 A HK68996 A HK 68996A
- Authority
- HK
- Hong Kong
- Prior art keywords
- compound
- oxepin
- dihydrodibenz
- group
- solution
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D313/00—Heterocyclic compounds containing rings of more than six members having one oxygen atom as the only ring hetero atom
- C07D313/02—Seven-membered rings
- C07D313/06—Seven-membered rings condensed with carbocyclic rings or ring systems
- C07D313/10—Seven-membered rings condensed with carbocyclic rings or ring systems condensed with two six-membered rings
- C07D313/12—[b,e]-condensed
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pyrane Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Claims (9)
1. Dibenz[b,e]oxepin-Verbindung der Formel (I)
in der der Rest A eine Carboxylgruppe, einen gerad- oder verzweigtkettigen C1-C6-Alkoxycarbonylrest, einen Rest der Formel -CONHOH oder -CONR1 R2 bedeutet, in der R1 und R2 gleich oder verschieden sind und ein Wasserstoffatom oder einen gerad- oder verzweigtkettigen C1-C6-Alkylrest darstellen;
Y die Bedeutung -(CH2)m-, -CHR3-(CH2)m- oder -CR4 =CR5-(CH2)m- hat, wobei R3 einen gerad- oder verzweigtkettigen C1-C6-Alkylrest, oder einen Niederalkylrest bedeutet, R4 und R5 gleich oder verschieden sind und ein Wasserstoffatom oder einen gerad- oder verzweigtkettigen C1-C6-Alkylrest darstellen und m den Wert 1, 2, 3 oder 4 hat, der den Substituenten in 2- oder 3-Stellung am Hauptkern darstellt, wobei die linke Seite des Restes Y an den Benzolring gebunden ist,
X die Gruppen = N- oder = CH- bedeutet,
n den Wert 0, 1, 2, 3 oder 4 hat,
Z eine 4-Methylpiperazino-, 4-Methylhomopiperazino-, Piperidino-, Pyrrolidino-, Thiomorpholino-, Morpholinogruppe oder den Rest mit der Formel -NR6R7 bedeutet, in der R6 und R7 gleich oder verschieden sind und ein Wasserstoffatom oder einen gerad- oder verzweigtkettigen Ci-6-Alkylrest bedeuten und das Symbol eine Doppelbindung bedeutet, und pharmazeutisch verträgliche Salze davon.
2. Verbindung nach Anspruch 1, wobei das Salz ausgewählt ist aus einem Säureadditionssalz, Metallsalz, Ammoniumsalz, organischen Aminadditionssalz und Aminosäureadditionssalz.
3. Verbindung nach Anspruch 1, wobei der Rest A ausgewählt ist aus gerad- oder verzweigtkettigen Ci - C6-Alkoxycarbonylresten, dem Rest der Formel -CONR1R2 und der Carboxylgruppe, Y in der 2-Stellung des Hauptkerns gebunden ist, X ausgewählt ist aus den Gruppen = N- und = CH-, n den Wert 1 oder 2 hat und Z ausgewählt ist aus der Dimethylamino-, Diethylamino-, Methylamino-, Amino-, Morpholino- und Thiomorpholinogruppe.
4. Verbindung nach Anspruch 3, wobei der Rest Y ausgewählt ist aus -(CH2)m-,
und -CH = CH-(CH2)m-und m den Wert 1 oder 2 hat.
5. Verbindung nach Anspruch 4, wobei der Rest A eine Carboxylgruppe bedeutet und X die Gruppe = CH- darstellt.
6. Verbindung nach Anspruch 1, wobei der Rest der Formel -Y-A die Carboxymethyl- oder 2-Carboxyethylgruppe bedeutet, X die Gruppe = CH- bedeutet und n den Wert 2 hat und Z ausgewählt ist aus der Dimethylamino-, Diethylamino-, Methylamino-, Amino-, Morpholino- und Thiomorpholinogruppe.
7. Verbindung nach Anspruch 1, wobei der Rest der Formel -Y-A die Gruppe 2-CH2COOH bedeutet, X die Gruppe = CH-bedeutet, n den Wert 2 hat und Z eine Dimethylaminogruppe darstellt.
8. Verbindung nach Anspruch 1, wobei der Rest der Formel -Y-A die Gruppe 2-CH2CH2COOH bedeutet, X die Gruppe = CH-bedeutet, n den Wert 2 hat und Z eine Dimethylaminogruppe darstellt.
9. Verwendung einer Verbindung gemäß einem der Ansprüche 1 bis 8 zur Herstellung von Arzneimitteln zur therapeutischen Behandlung von allergischen und entzündlichen Erkrankungen.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4567686 | 1986-03-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HK68996A true HK68996A (en) | 1996-04-26 |
Family
ID=12725992
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HK68996A HK68996A (en) | 1986-03-03 | 1996-04-18 | Dibenz [b,e] oxepin derivative and antiallergic and antiinflammatory agent |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US5116863A (de) |
| EP (1) | EP0235796B2 (de) |
| JP (1) | JPS6310784A (de) |
| DE (1) | DE3778734D1 (de) |
| ES (1) | ES2038608T5 (de) |
| HK (1) | HK68996A (de) |
| MX (1) | MX9203155A (de) |
Families Citing this family (76)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4882351A (en) * | 1987-10-14 | 1989-11-21 | Roussel Uclaf | Tricyclic compounds |
| AU612437B2 (en) * | 1987-12-14 | 1991-07-11 | Kyowa Hakko Kogyo Co. Ltd. | Tricyclic compounds |
| US5242931A (en) * | 1988-06-09 | 1993-09-07 | Kyowa Hakko Kogyo Co., Ltd. | Tricyclic compounds as TXA2 antagonists |
| US4999363A (en) * | 1988-06-09 | 1991-03-12 | Kyowa Hakko Kogyo Co., Ltd. | Tricyclic compounds |
| GB8914061D0 (en) * | 1989-06-19 | 1989-08-09 | Wellcome Found | Agents for potentiating the effects of antitumour agents and combating multiple drug resistance |
| TW209861B (de) * | 1989-08-25 | 1993-07-21 | Hoechst Roussel Pharma | |
| US5840749A (en) * | 1989-08-25 | 1998-11-24 | Hoechst Marion Roussel, Inc. | N-hydroxy-dibenz b,e!oxepinalkylamines, N-hydroxy-dibenz b,e!oxepinalkanoic acid amides and related heterocyclic analogues |
| US5574173A (en) * | 1993-12-06 | 1996-11-12 | Schering Corporation | Tricyclic derivatives, compositions and methods of use |
| DE69427023T2 (de) * | 1993-12-28 | 2001-10-31 | Meiji Seika K.K., Tokio/Tokyo | Tricyclische benzazepin-und benzothiazepin derivate |
| US5641805A (en) * | 1995-06-06 | 1997-06-24 | Alcon Laboratories, Inc. | Topical ophthalmic formulations for treating allergic eye diseases |
| WO1997014672A1 (en) * | 1995-10-16 | 1997-04-24 | Kyowa Hakko Kogyo Co. Ltd. | Triciclic compounds |
| US6323206B1 (en) | 1996-07-12 | 2001-11-27 | Millennium Pharmaceuticals, Inc. | Chemokine receptor antagonists and methods of use therefor |
| AU729415B2 (en) | 1996-07-12 | 2001-02-01 | Millennium Pharmaceuticals, Inc. | Chemokine receptor antagonists and methods of use therefor |
| HUP0002461A3 (en) | 1997-04-15 | 2003-01-28 | Kyowa Hakko Kogyo Kk | Tricyclic benzothiepin a benzoxepin derivatives and pharmaceutical compositions thereof |
| US6613905B1 (en) * | 1998-01-21 | 2003-09-02 | Millennium Pharmaceuticals, Inc. | Chemokine receptor antagonists and methods of use therefor |
| AU2331999A (en) | 1998-01-21 | 1999-08-09 | Kyowa Hakko Kogyo Co. Ltd. | Chemokine receptor antagonists and methods of use therefor |
| CA2318088A1 (en) | 1998-01-21 | 1999-07-29 | Yoshisuke Nakasato | Chemokine receptor antagonists and methods of use therefor |
| US6509346B2 (en) | 1998-01-21 | 2003-01-21 | Millennium Pharmaceuticals, Inc. | Chemokine receptor antagonists and methods of use therefor |
| DE69900207T2 (de) * | 1998-07-14 | 2001-11-22 | Alcon Laboratories, Inc. | Verwendung von 11-(3-dimethylaminopropyliden)-6,11-dihydrodibenz[b,e]oxepin-2-essigsäure und deren pharmazeutisch annehmbaren salzen zur herstellung eines medikaments zur behandlung nicht-allergisch-bedingten augenentzündungen und zur prevention der okularen neovaskularisation |
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| US20040097486A1 (en) * | 1999-11-18 | 2004-05-20 | Yanni John M. | Use of an H1 antagonist and a safe steroid to treat eye conditions |
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| US7977376B2 (en) | 2001-06-27 | 2011-07-12 | Novartis Ag | Olopatadine formulations for topical nasal administration |
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| JP4022519B2 (ja) * | 2001-11-13 | 2007-12-19 | 協和醗酵工業株式会社 | そう痒の予防または治療剤 |
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| KR20050044550A (ko) * | 2001-12-05 | 2005-05-12 | 알콘, 인코퍼레이티드 | 비염 치료를 위한 η1 길항제 및 안전한 스테로이드제의용도 |
| TWI291467B (en) * | 2002-11-13 | 2007-12-21 | Millennium Pharm Inc | CCR1 antagonists and methods of use therefor |
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| WO2005102313A1 (ja) * | 2004-04-21 | 2005-11-03 | Kyowa Hakko Kogyo Co., Ltd. | 慢性副鼻腔炎の予防および/または治療剤 |
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| CA2573915A1 (en) * | 2004-07-16 | 2006-01-26 | Kyowa Hakko Kogyo Co., Ltd. | Preventive and/or therapeutic agent for sleeping disorder |
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| JP5139104B2 (ja) * | 2007-02-16 | 2013-02-06 | 住友化学株式会社 | ジベンゾオキセピン化合物の製造方法 |
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| JP5248078B2 (ja) * | 2007-10-05 | 2013-07-31 | 住友化学株式会社 | ジベンゾオキセピン化合物の製造方法 |
| EP2666770A1 (de) * | 2008-07-16 | 2013-11-27 | Crystal Pharma S.A.U | Verfahren zur Herstellung von Olopatadin und Zwischenprodukten |
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| US8642069B2 (en) * | 2008-08-27 | 2014-02-04 | Alexander D. Goldin | Composition and method for treating colds |
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| IT1397503B1 (it) | 2009-04-21 | 2013-01-16 | F S I Fabbrica Italiana Sint | Processo per la preparazione di olopatadina |
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| WO2011033532A1 (en) | 2009-09-17 | 2011-03-24 | Indoco Remedies Limited | Process for preparation of olopatadine hydrochloride |
| CN102548536A (zh) * | 2009-10-01 | 2012-07-04 | 爱尔康研究有限公司 | 奥洛他定组合物及其用途 |
| WO2011128911A2 (en) * | 2010-04-12 | 2011-10-20 | Msn Laboratories Limited | Improved process for ll-[(z)-3-(dimethylamino)propyiidenel-6-ll- dihydrodibenz[b,el oxepin-2-aceticacid |
| WO2011141929A2 (en) | 2010-05-11 | 2011-11-17 | Cadila Healthcare Limited | Aqueous pharmaceutical compositions of fluticasone and olopatadine |
| TW201206936A (en) | 2010-07-19 | 2012-02-16 | Alcon Res Ltd | Methods and compositions for the treatment of allergy |
| TWI544922B (zh) | 2011-05-19 | 2016-08-11 | 愛爾康研究有限公司 | 高濃度歐羅派特錠(olopatadine)眼用組成物 |
| TW201336527A (zh) | 2012-02-10 | 2013-09-16 | Alcon Res Ltd | 具增強的穩定性之水性藥學組成物 |
| CN103664861B (zh) * | 2013-12-18 | 2018-01-30 | 北京华禧联合科技发展有限公司 | 一种用高活性有机锌试剂制备盐酸奥洛他定的新方法 |
| JP7424115B2 (ja) * | 2019-06-26 | 2024-01-30 | 住友化学株式会社 | エステル化合物の製造方法 |
| CN111548369B (zh) * | 2020-05-29 | 2023-02-28 | 内蒙古京东药业有限公司 | 一种简便制备高纯度奥洛他定盐酸盐中间体的方法 |
| CN112457287B (zh) * | 2020-12-09 | 2024-02-06 | 重庆西南制药二厂有限责任公司 | 一种e-奥洛他定的制备方法 |
| CN114380783B (zh) * | 2022-01-18 | 2023-02-10 | 梯尔希(南京)药物研发有限公司 | 一种奥洛他定氘标记代谢物的制备方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE641498A (de) * | 1962-03-13 | |||
| US3420851A (en) * | 1962-12-19 | 1969-01-07 | Pfizer & Co C | Novel dibenzoxepines |
| FR88751E (de) * | 1963-07-09 | 1967-06-07 | ||
| SE368825B (de) * | 1963-10-14 | 1974-07-22 | Pfizer | |
| DE1543346A1 (de) * | 1966-04-30 | 1969-09-25 | Boehringer Mannheim Gmbh | Verfahren zur Herstellung basischer Derivate des Dibenzoxepins und Dibenzothiepins |
| US4585788A (en) * | 1973-09-06 | 1986-04-29 | American Hoechst Corporation | 6,11-dihydrodibenz[b,e]oxepin-acetic acids and derivatives |
| US4282365A (en) * | 1978-11-24 | 1981-08-04 | Merck & Co., Inc. | Dibenz[b,e]oxepin compounds |
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| JPS58126883A (ja) * | 1982-01-25 | 1983-07-28 | Kyowa Hakko Kogyo Co Ltd | ジベンゾ〔b,e〕オキセピン誘導体を含有してなる抗喘息剤 |
| JPS59227879A (ja) * | 1983-06-10 | 1984-12-21 | Kyowa Hakko Kogyo Co Ltd | ジベンゾ[b,e]オキセピン誘導体 |
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-
1987
- 1987-02-27 JP JP62044678A patent/JPS6310784A/ja active Granted
- 1987-03-02 US US07/020,900 patent/US5116863A/en not_active Expired - Lifetime
- 1987-03-03 DE DE8787102983T patent/DE3778734D1/de not_active Expired - Lifetime
- 1987-03-03 EP EP87102983A patent/EP0235796B2/de not_active Expired - Lifetime
- 1987-03-03 ES ES87102983T patent/ES2038608T5/es not_active Expired - Lifetime
-
1992
- 1992-06-23 MX MX9203155A patent/MX9203155A/es active IP Right Grant
-
1996
- 1996-04-18 HK HK68996A patent/HK68996A/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0586925B2 (de) | 1993-12-14 |
| EP0235796A2 (de) | 1987-09-09 |
| EP0235796B1 (de) | 1992-05-06 |
| MX9203155A (es) | 1992-07-01 |
| EP0235796B2 (de) | 1997-03-12 |
| ES2038608T5 (es) | 1997-07-16 |
| JPS6310784A (ja) | 1988-01-18 |
| EP0235796A3 (en) | 1988-09-21 |
| DE3778734D1 (de) | 1992-06-11 |
| US5116863A (en) | 1992-05-26 |
| ES2038608T3 (es) | 1993-08-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PF | Patent in force | ||
| PE | Patent expired |
Effective date: 20070302 |