CN1170814C - 用于强化胆碱能活性的酰胺化合物 - Google Patents
用于强化胆碱能活性的酰胺化合物 Download PDFInfo
- Publication number
- CN1170814C CN1170814C CNB008043035A CN00804303A CN1170814C CN 1170814 C CN1170814 C CN 1170814C CN B008043035 A CNB008043035 A CN B008043035A CN 00804303 A CN00804303 A CN 00804303A CN 1170814 C CN1170814 C CN 1170814C
- Authority
- CN
- China
- Prior art keywords
- compound
- salt
- mixture
- reaction
- aryl
- 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 - Fee Related
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
- C07C233/65—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/28—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C275/30—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by halogen atoms, or by nitro or nitroso groups
-
- 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
- C07D211/68—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 one double bond between ring members or between a ring member and a non-ring member
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/02—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
- C07D217/06—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with the ring nitrogen atom acylated by carboxylic or carbonic acids, or with sulfur or nitrogen analogues thereof, e.g. carbamates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/16—Systems containing only non-condensed rings with a six-membered ring the ring being unsaturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/10—One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Psychiatry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AUPP8912A AUPP891299A0 (en) | 1999-02-26 | 1999-02-26 | New 6-membered cyclic compounds |
| AUPP8912 | 1999-02-26 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1341095A CN1341095A (zh) | 2002-03-20 |
| CN1170814C true CN1170814C (zh) | 2004-10-13 |
Family
ID=3813111
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB008043035A Expired - Fee Related CN1170814C (zh) | 1999-02-26 | 2000-02-03 | 用于强化胆碱能活性的酰胺化合物 |
Country Status (19)
| Country | Link |
|---|---|
| EP (1) | EP1159258B1 (https=) |
| JP (1) | JP4089159B2 (https=) |
| KR (1) | KR100620406B1 (https=) |
| CN (1) | CN1170814C (https=) |
| AR (1) | AR029618A1 (https=) |
| AT (1) | ATE282022T1 (https=) |
| AU (2) | AUPP891299A0 (https=) |
| BR (1) | BR0010225A (https=) |
| CA (1) | CA2371827C (https=) |
| DE (1) | DE60015732T2 (https=) |
| DK (1) | DK1159258T3 (https=) |
| ES (1) | ES2226775T3 (https=) |
| HK (1) | HK1044934B (https=) |
| HU (1) | HUP0200116A3 (https=) |
| PT (1) | PT1159258E (https=) |
| RU (1) | RU2211215C2 (https=) |
| TR (1) | TR200102494T2 (https=) |
| TW (1) | TWI225856B (https=) |
| WO (1) | WO2000051970A1 (https=) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000030446A1 (en) | 1998-11-23 | 2000-06-02 | Bonnie Davis | Dosage formulations for acetylcholinesterase inhibitors |
| EE04996B1 (et) | 1998-12-24 | 2008-04-15 | Janssen Pharmaceutica N.V. | Reguleeritud vabanemisega galantamiinipreparaat, meetod selle valmistamiseks, seda sisaldav doseerimisvorm ning farmatseutiline pakend |
| TWI243164B (en) | 2001-02-13 | 2005-11-11 | Aventis Pharma Gmbh | Acylated indanyl amines and their use as pharmaceuticals |
| PE20020870A1 (es) | 2001-02-13 | 2002-11-18 | Aventis Pharma Gmbh | 6,7,8,9-tetrahidro-5h-benzocicloheptenil aminas aciladas |
| TWI241190B (en) * | 2001-02-13 | 2005-10-11 | Aventis Pharma Gmbh | 4-Fluoro-N-indan-2-yl benzamide and its use as pharmaceutical |
| PE20020856A1 (es) * | 2001-02-13 | 2002-11-11 | Aventis Pharma Gmbh | 1,2,3,4-tetrahidronaftil aminas aciladas |
| WO2003097586A1 (en) * | 2002-05-17 | 2003-11-27 | Janssen Pharmaceutica N.V. | Aminotetralin-derived urea modulators of vanilloid vr1 receptor |
| BRPI0413347A (pt) | 2003-08-06 | 2006-10-10 | Senomyx Inc | novos sabores, modificadores de sabor, agentes de sabor, realçadores de sabor, agentes de sabor e/ou realçadores umami ou doces, e utilização correspondente |
| KR101387563B1 (ko) | 2006-04-21 | 2014-04-25 | 세노믹스, 인코포레이티드 | 고효능의 조미용 향료를 포함하는 식품 조성물 및 이의 제조 방법 |
| EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| UY32442A (es) | 2009-02-13 | 2010-09-30 | Sanofi Aventis | Nuevos indanos sustituidos, procesos para su preparacion y uso de los mismos como un medicamento |
| JP2025066196A (ja) * | 2022-03-14 | 2025-04-23 | 国立大学法人東北大学 | 認知機能改善剤 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR8287M (https=) * | 1968-12-31 | 1970-11-09 | ||
| US4797419A (en) * | 1986-11-03 | 1989-01-10 | Warner-Lambert Company | Method of treating the symptoms of senile cognitive decline employing di- or trisubstituted urea cholinergic agents |
| EP0306375A1 (fr) * | 1987-08-07 | 1989-03-08 | Synthelabo | Dérivés de[(pipéridinyl-4)méthyl]-2 tétrahydro-1,2,3,4 isoquinoléine, leur préparation et leur application en thérapeutique |
| IL90279A (en) * | 1988-05-24 | 1995-03-30 | American Home Prod | Piperazinyl carboxamide derivatives, their preparation and pharmaceutical com¦ositions containing them |
| GB8917687D0 (en) * | 1989-08-02 | 1989-09-20 | Fujisawa Pharmaceutical Co | Aminopiperazine derivatives,processes for preparation thereof and pharmaceutical composition comprising the same |
| RU2024507C1 (ru) * | 1991-11-18 | 1994-12-15 | Евгений Яковлевич Левитин | 5-хлор-2-пиридиламид-4-нитро-n-(карбоксиметил)антраниловой кислоты, проявляющий противовоспалительную активность |
| JPH06107544A (ja) * | 1992-09-29 | 1994-04-19 | Taisho Pharmaceut Co Ltd | コリン作動性神経不全の改善・治療薬 |
| JPH06298732A (ja) * | 1993-02-16 | 1994-10-25 | Taisho Pharmaceut Co Ltd | インドール誘導体 |
-
1999
- 1999-02-26 AU AUPP8912A patent/AUPP891299A0/en not_active Abandoned
-
2000
- 2000-02-03 AU AU23257/00A patent/AU766655B2/en not_active Ceased
- 2000-02-03 KR KR1020017010325A patent/KR100620406B1/ko not_active Expired - Fee Related
- 2000-02-03 PT PT00902080T patent/PT1159258E/pt unknown
- 2000-02-03 RU RU2001126120/04A patent/RU2211215C2/ru not_active IP Right Cessation
- 2000-02-03 HU HU0200116A patent/HUP0200116A3/hu unknown
- 2000-02-03 BR BR0010225-3A patent/BR0010225A/pt not_active Application Discontinuation
- 2000-02-03 DE DE60015732T patent/DE60015732T2/de not_active Expired - Lifetime
- 2000-02-03 CN CNB008043035A patent/CN1170814C/zh not_active Expired - Fee Related
- 2000-02-03 DK DK00902080T patent/DK1159258T3/da active
- 2000-02-03 AT AT00902080T patent/ATE282022T1/de not_active IP Right Cessation
- 2000-02-03 EP EP00902080A patent/EP1159258B1/en not_active Expired - Lifetime
- 2000-02-03 JP JP2000602198A patent/JP4089159B2/ja not_active Expired - Fee Related
- 2000-02-03 CA CA002371827A patent/CA2371827C/en not_active Expired - Fee Related
- 2000-02-03 HK HK02106646.3A patent/HK1044934B/zh not_active IP Right Cessation
- 2000-02-03 WO PCT/JP2000/000601 patent/WO2000051970A1/en not_active Ceased
- 2000-02-03 ES ES00902080T patent/ES2226775T3/es not_active Expired - Lifetime
- 2000-02-03 TR TR2001/02494T patent/TR200102494T2/xx unknown
- 2000-02-14 TW TW089102410A patent/TWI225856B/zh not_active IP Right Cessation
- 2000-02-24 AR ARP000100793A patent/AR029618A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP1159258A1 (en) | 2001-12-05 |
| BR0010225A (pt) | 2002-01-22 |
| JP4089159B2 (ja) | 2008-05-28 |
| CN1341095A (zh) | 2002-03-20 |
| ES2226775T3 (es) | 2005-04-01 |
| HK1044934B (zh) | 2005-06-03 |
| RU2211215C2 (ru) | 2003-08-27 |
| TWI225856B (en) | 2005-01-01 |
| AR029618A1 (es) | 2003-07-10 |
| DE60015732T2 (de) | 2005-03-31 |
| EP1159258B1 (en) | 2004-11-10 |
| PT1159258E (pt) | 2005-02-28 |
| CA2371827C (en) | 2008-06-10 |
| TR200102494T2 (tr) | 2002-01-21 |
| AUPP891299A0 (en) | 1999-03-25 |
| HK1044934A1 (en) | 2002-11-08 |
| DE60015732D1 (de) | 2004-12-16 |
| AU766655B2 (en) | 2003-10-23 |
| HUP0200116A3 (en) | 2002-11-28 |
| WO2000051970A1 (en) | 2000-09-08 |
| CA2371827A1 (en) | 2000-09-08 |
| KR100620406B1 (ko) | 2006-09-13 |
| AU2325700A (en) | 2000-09-21 |
| HUP0200116A2 (hu) | 2002-05-29 |
| DK1159258T3 (da) | 2005-02-14 |
| KR20010102140A (ko) | 2001-11-15 |
| ATE282022T1 (de) | 2004-11-15 |
| JP2002538132A (ja) | 2002-11-12 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN1067067C (zh) | 杂环速激肽受体拮抗物 | |
| CN1123564C (zh) | 抗炎化合物 | |
| CN1041203C (zh) | 吡唑并吡啶化合物的制备方法 | |
| CN1213046C (zh) | 四氢吡啶衍生物,它们的制备和它们作为细胞增殖抑制剂的应用 | |
| CN1170814C (zh) | 用于强化胆碱能活性的酰胺化合物 | |
| CN1289481C (zh) | 作为降低脂质剂的联苯甲酰胺化合物 | |
| CN1113059C (zh) | 用作神经激肽拮抗剂的哌嗪并衍生物 | |
| CN1340044A (zh) | 莫维诺林衍生物 | |
| CN1729173A (zh) | N-(吲哚乙基)环胺化合物 | |
| CN1414956A (zh) | 作为mip抑制剂的经取代的哌嗪衍生物 | |
| CN1212835C (zh) | 含异羟肟酸酯的半胱氨酸和丝氨酸蛋白酶抑制剂 | |
| CN1343197A (zh) | 作为神经激肽-1受体拮抗剂的联苯基衍生物 | |
| CN1097006A (zh) | O-芳基吗啡喃的醚类化合物 | |
| CN1404467A (zh) | 氨基磺酰基联苯基衍生物 | |
| CN1278789A (zh) | 作为磷脂酶抑制剂的9,10-二氢-9,10-桥亚乙基蒽衍生物 | |
| US7241811B2 (en) | Amide compounds for the potentiation of cholinergic activity | |
| CN1164580C (zh) | 用作5-羟色胺激活剂的二唑衍生物 | |
| CN1167694C (zh) | 1-苯基-4-(1-[2-芳基]环丙基)甲基哌嗪:多巴胺受体配体 | |
| CN1185214C (zh) | 新的茚并吲哚酮化合物,其制备方法和含有这种化合物的药物组合物 | |
| CN1227230C (zh) | Nmda受体配体的前药 | |
| CN1100033C (zh) | 苯乙醇氨基-1,2,3,4-四氢化萘氧烃基酰胺衍生物 | |
| RU2181119C2 (ru) | Новые производные феноксиэтиламина, способ их получения, их применение в качестве лекарственных средств и содержащие их фармацевтические композиции | |
| CN1183765A (zh) | 对5-ht1a受体具高度亲和力的苯氧乙胺衍生物,其制备方法、作为药物的用途及含有它们的药物组合物 | |
| CN1863769A (zh) | 氨基吡咯烷衍生物的制备方法和中间体化合物 | |
| CN1753870A (zh) | 新的苯甲酰胺衍生物及其制备方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C06 | Publication | ||
| PB01 | Publication | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C56 | Change in the name or address of the patentee |
Owner name: ASTELLAS PHARMA INC. Free format text: FORMER NAME OR ADDRESS: FUJISAWA PHARMACEUTICAL CO., LTD. |
|
| CP03 | Change of name, title or address |
Address after: Tokyo, Japan Patentee after: Yamanouchi Pharma Co., Ltd. Address before: Osaka City, Osaka of Japan Patentee before: Fujisawa Pharmaceutical Co., Ltd. |
|
| C17 | Cessation of patent right | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20041013 Termination date: 20100203 |