CN101052618A - 用作治疗阿尔茨海默氏病的β-分泌酶抑制剂的2-氨基吡啶化合物 - Google Patents
用作治疗阿尔茨海默氏病的β-分泌酶抑制剂的2-氨基吡啶化合物 Download PDFInfo
- Publication number
- CN101052618A CN101052618A CNA2005800376837A CN200580037683A CN101052618A CN 101052618 A CN101052618 A CN 101052618A CN A2005800376837 A CNA2005800376837 A CN A2005800376837A CN 200580037683 A CN200580037683 A CN 200580037683A CN 101052618 A CN101052618 A CN 101052618A
- Authority
- CN
- China
- Prior art keywords
- alkyl
- compound
- halogen
- aryl
- hydrogen
- 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.)
- Pending
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
- C07D213/72—Nitrogen atoms
- C07D213/73—Unsubstituted amino or imino radicals
-
- 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
-
- 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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US62344104P | 2004-10-29 | 2004-10-29 | |
| US60/623,441 | 2004-10-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN101052618A true CN101052618A (zh) | 2007-10-10 |
Family
ID=36565355
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNA2005800376837A Pending CN101052618A (zh) | 2004-10-29 | 2005-10-25 | 用作治疗阿尔茨海默氏病的β-分泌酶抑制剂的2-氨基吡啶化合物 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7932275B2 (https=) |
| EP (1) | EP1807396B1 (https=) |
| JP (1) | JP2008518969A (https=) |
| CN (1) | CN101052618A (https=) |
| AU (1) | AU2005310239A1 (https=) |
| CA (1) | CA2585279A1 (https=) |
| WO (1) | WO2006060109A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111533684A (zh) * | 2020-05-29 | 2020-08-14 | 四川大学 | 一种吡啶化合物烯基化的方法 |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7763609B2 (en) | 2003-12-15 | 2010-07-27 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| AU2006306542B2 (en) * | 2005-10-21 | 2012-04-19 | Merck Sharp & Dohme Corp. | Potassium channel inhibitors |
| EP2418202B1 (en) | 2006-03-31 | 2014-01-29 | Novartis AG | (4-[4-[5-(substituted amino)-pyridin-2-yl]phenyl]-cyclohexyl)-acetic acid derivatives as DGAT inhibitors |
| US8278345B2 (en) | 2006-11-09 | 2012-10-02 | Probiodrug Ag | Inhibitors of glutaminyl cyclase |
| ATE554085T1 (de) | 2006-11-30 | 2012-05-15 | Probiodrug Ag | Neue inhibitoren von glutaminylcyclase |
| JP5930573B2 (ja) | 2007-03-01 | 2016-06-15 | プロビオドルグ エージー | グルタミニルシクラーゼ阻害剤の新規使用 |
| EP2142514B1 (en) | 2007-04-18 | 2014-12-24 | Probiodrug AG | Thiourea derivatives as glutaminyl cyclase inhibitors |
| AR066169A1 (es) | 2007-09-28 | 2009-07-29 | Novartis Ag | Derivados de benzo-imidazoles, utiles para trastornos asociados con la actividad de dgat |
| AU2009217518A1 (en) * | 2008-02-28 | 2009-09-03 | Merck Sharp & Dohme Corp. | 2-aminoimidazole beta-secretase inhibitors for the treatment of Alzheimer's disease |
| JP5934645B2 (ja) | 2009-09-11 | 2016-06-15 | プロビオドルグ エージー | グルタミニルシクラーゼ阻害剤としてのヘテロ環式誘導体 |
| UA108363C2 (uk) | 2009-10-08 | 2015-04-27 | Похідні імінотіадіазиндіоксиду як інгібітори bace, композиція на їх основі і їх застосування | |
| JP6026284B2 (ja) | 2010-03-03 | 2016-11-16 | プロビオドルグ エージー | グルタミニルシクラーゼの阻害剤 |
| NZ602312A (en) | 2010-03-10 | 2014-02-28 | Probiodrug Ag | Heterocyclic inhibitors of glutaminyl cyclase (qc, ec 2.3.2.5) |
| WO2011131748A2 (en) | 2010-04-21 | 2011-10-27 | Probiodrug Ag | Novel inhibitors |
| EP2686313B1 (en) | 2011-03-16 | 2016-02-03 | Probiodrug AG | Benzimidazole derivatives as inhibitors of glutaminyl cyclase |
| EP2694521B1 (en) | 2011-04-07 | 2015-11-25 | Merck Sharp & Dohme Corp. | Pyrrolidine-fused thiadiazine dioxide compounds as bace inhibitors, compositions, and their use |
| EP2694489B1 (en) | 2011-04-07 | 2017-09-06 | Merck Sharp & Dohme Corp. | C5-c6 oxacyclic-fused thiadiazine dioxide compounds as bace inhibitors, compositions, and their use |
| CN103874496A (zh) | 2011-08-22 | 2014-06-18 | 默沙东公司 | 作为bace抑制剂的2-螺-取代的亚氨基噻嗪类及其单和二氧化物、组合物及其用途 |
| ES2812698T3 (es) | 2017-09-29 | 2021-03-18 | Probiodrug Ag | Inhibidores de glutaminil ciclasa |
| US11339161B2 (en) * | 2017-12-19 | 2022-05-24 | Boehringer Ingelheim International Gmbh | Triazolo pyridines as modulators of gamma-secretase |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IE82916B1 (en) * | 1990-11-02 | 2003-06-11 | Elan Corp Plc | Formulations and their use in the treatment of neurological diseases |
| CN1446202A (zh) * | 2000-08-11 | 2003-10-01 | 卫材株式会社 | 2-氨基吡啶化合物及其作为药物的用途 |
| US6951946B2 (en) * | 2002-03-19 | 2005-10-04 | Lexicon Pharmaceuticals, Inc. | Large scale synthesis of 1,2,4- and 1,3,4-oxadiazole carboxylates |
| WO2003106405A1 (en) | 2002-06-01 | 2003-12-24 | Sunesis Pharmaceuticals, Inc. | Aspartyl protease inhibitors |
| GB0305918D0 (en) | 2003-03-14 | 2003-04-23 | Glaxo Group Ltd | Novel compounds |
| CA2529739A1 (en) | 2003-06-16 | 2005-01-20 | Sunesis Pharmaceuticals, Inc. | Aspartyl protease inhibitors |
| US20080287399A1 (en) | 2004-12-14 | 2008-11-20 | Astrazeneca Ab | Substituted Aminopyridines and Uses Thereof |
-
2005
- 2005-10-25 WO PCT/US2005/039932 patent/WO2006060109A1/en not_active Ceased
- 2005-10-25 JP JP2007539354A patent/JP2008518969A/ja active Pending
- 2005-10-25 CN CNA2005800376837A patent/CN101052618A/zh active Pending
- 2005-10-25 AU AU2005310239A patent/AU2005310239A1/en not_active Abandoned
- 2005-10-25 CA CA002585279A patent/CA2585279A1/en not_active Abandoned
- 2005-10-25 EP EP05851361.5A patent/EP1807396B1/en not_active Expired - Lifetime
- 2005-10-25 US US11/666,942 patent/US7932275B2/en active Active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111533684A (zh) * | 2020-05-29 | 2020-08-14 | 四川大学 | 一种吡啶化合物烯基化的方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| US7932275B2 (en) | 2011-04-26 |
| WO2006060109B1 (en) | 2006-08-10 |
| AU2005310239A1 (en) | 2006-06-08 |
| EP1807396B1 (en) | 2013-06-26 |
| EP1807396A1 (en) | 2007-07-18 |
| CA2585279A1 (en) | 2006-06-08 |
| EP1807396A4 (en) | 2009-09-09 |
| JP2008518969A (ja) | 2008-06-05 |
| WO2006060109A1 (en) | 2006-06-08 |
| US20080161363A1 (en) | 2008-07-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101052618A (zh) | 用作治疗阿尔茨海默氏病的β-分泌酶抑制剂的2-氨基吡啶化合物 | |
| CN1093130C (zh) | 被取代的吡啶并6,6-二环衍生物 | |
| CN1191236C (zh) | 取代的6,6-杂-双环衍生物 | |
| CN1859904A (zh) | 用于治疗阿尔茨海默氏病的苄醚和苄氨基β-分泌酶抑制剂 | |
| CN1443165A (zh) | 环戊二烯并吲哚、含有这类化合物的组合物及治疗方法 | |
| CN1835936A (zh) | 用于治疗阿尔茨海默氏病的大环β-分泌酶抑制剂 | |
| CN1045580A (zh) | 吡咯烷衍生物 | |
| CN1909897A (zh) | 用于治疗阿尔茨海默病的苯基羧化物β-分泌酶抑制剂 | |
| CN1968924A (zh) | 作为β-分泌酶抑制剂用于治疗阿尔茨海默氏病的吡咯烷-3-基化合物 | |
| CN1735597A (zh) | 作为前列腺素激动剂的2-哌啶酮衍生物 | |
| CN1206407A (zh) | 取代的乙烯基吡啶衍生物和含有它们的药物 | |
| CN101035760A (zh) | 增强谷氨酸受体的化合物及其在药物中的应用 | |
| CN1768055A (zh) | 作为代谢型谷氨酸受体-5调制剂的四环咪唑衍生物 | |
| CN1142827A (zh) | Hiv蛋白酶抑制剂 | |
| CN1525972A (zh) | 杂双环crf拮抗剂 | |
| CN1798744A (zh) | 作为nmda/nr2b拮抗剂的3-氟-哌啶化合物 | |
| CN101061119A (zh) | 治疗阿尔茨海默氏病的大环氨基吡啶β-分泌酶抑制剂 | |
| CN1256337C (zh) | 抗抑郁的7,8-二氢-1,6,9-三氧杂-3-氮杂-环戊二烯并[a]萘的氮杂环基甲基衍生物 | |
| JP2020518555A (ja) | 複素環p2x7アンタゴニスト | |
| CN1267434C (zh) | 抗抑郁的(SSSRI)7,8-二氢-3H-6,9-二氧杂-1,3-二氮杂环戊二烯并[a]萘的氮杂环基甲基衍生物 | |
| CN101035533A (zh) | 抗精神分裂症的双重nk1/nk3拮抗剂 | |
| CN1017901B (zh) | 抗精神病药稠环吡啶基哌嗪衍生物的制备方法 | |
| CN1960971A (zh) | 取代的吡咯烷-2-酮 | |
| CN101068787A (zh) | 8-苯基-5,6,7,8-氢喹啉速激肽受体拮抗剂 | |
| CN1377269A (zh) | 玻璃体结合蛋白受体拮抗剂 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| AD01 | Patent right deemed abandoned |
Effective date of abandoning: 20071010 |
|
| C20 | Patent right or utility model deemed to be abandoned or is abandoned |