NO20025651L - Adenosin A2A-reseptorantagonister - Google Patents
Adenosin A2A-reseptorantagonisterInfo
- Publication number
- NO20025651L NO20025651L NO20025651A NO20025651A NO20025651L NO 20025651 L NO20025651 L NO 20025651L NO 20025651 A NO20025651 A NO 20025651A NO 20025651 A NO20025651 A NO 20025651A NO 20025651 L NO20025651 L NO 20025651L
- Authority
- NO
- Norway
- Prior art keywords
- optionally substituted
- phenyl
- parkinson
- heteroaryl
- disease
- Prior art date
Links
- 229940123702 Adenosine A2a receptor antagonist Drugs 0.000 title 1
- 239000002467 adenosine A2a receptor antagonist Substances 0.000 title 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 208000018737 Parkinson disease Diseases 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 238000002360 preparation method Methods 0.000 abstract 2
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 150000001721 carbon Chemical class 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000005982 diphenylmethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 1
- 125000003386 piperidinyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
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
- A61P25/00—Drugs for disorders of the nervous system
-
- 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
- A61P25/08—Antiepileptics; Anticonvulsants
-
- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P25/24—Antidepressants
-
- 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
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Det beskrives forbindelser med strukturformelen (I). eller et farmasøytisk aksepterbart salt derav, hvori R er om ønskelig substituert fenyl, sykloalkenyl eller heteroaryl, X er alkylen eller -C(0)CH-, Y er -N(R)CHCHN(R)-, - OCHCHN(R)-, -O-, -S-, -CHS-, -(CH)-NH-, eller eventuelt substituert, (Ia),m og n er 2-3, og Q er nitrogen eller eventuelt substituert karbon, og Z er eventuelt substituert fenyl, fenylalkyl eller heteroaryl, difenylmetyl, RC(0)-, R6-S02-, R6-OC(0)-, RN(R)-C(0)-, RN(R)-C(S)-, fenyl-CH(OH)- eller fenyl- C(=NOR) -, eller dersom Q er CH, a),. fenylamino eller pyridylamino, eller hvori Z og Y sammen er substituert piperidinyl eller substituert fenyl, og R, R, R, Rog Rer som definert i beskrivelsen, anvendelse av disse ved behandling av Parkinsons sykdom, alene eller i kombinasjon med andre midler for behandling av Parkinsons sykdom, og farmasøytiske preparater som inneholder dem; videre beskrives en fremgangsmåte for fremstilling av intermediater som er anvendbare for fremstilling av forbindelser med formel (I).
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US20714300P | 2000-05-26 | 2000-05-26 | |
| PCT/US2001/016954 WO2001092264A1 (en) | 2000-05-26 | 2001-05-24 | Adenosine a2a receptor antagonists |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO20025651D0 NO20025651D0 (no) | 2002-11-25 |
| NO20025651L true NO20025651L (no) | 2003-01-23 |
| NO325008B1 NO325008B1 (no) | 2008-01-14 |
Family
ID=22769372
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20025651A NO325008B1 (no) | 2000-05-26 | 2002-11-25 | Adenosin A2A-reseptorantagonister |
Country Status (31)
| Country | Link |
|---|---|
| US (4) | US6630475B2 (no) |
| EP (1) | EP1283839B1 (no) |
| JP (3) | JP4574112B2 (no) |
| KR (1) | KR100520907B1 (no) |
| CN (2) | CN1247588C (no) |
| AR (1) | AR028621A1 (no) |
| AT (1) | ATE293627T1 (no) |
| AU (2) | AU6808901A (no) |
| BR (1) | BRPI0111015B8 (no) |
| CA (1) | CA2410237C (no) |
| CZ (1) | CZ303790B6 (no) |
| DE (1) | DE60110219T2 (no) |
| DK (1) | DK1283839T3 (no) |
| EC (1) | ECSP024364A (no) |
| ES (1) | ES2237576T3 (no) |
| HK (1) | HK1049007B (no) |
| HU (1) | HU230420B1 (no) |
| IL (3) | IL152726A0 (no) |
| MX (1) | MXPA02011625A (no) |
| MY (1) | MY132006A (no) |
| NO (1) | NO325008B1 (no) |
| NZ (1) | NZ522326A (no) |
| PE (1) | PE20020062A1 (no) |
| PL (1) | PL218764B1 (no) |
| PT (1) | PT1283839E (no) |
| RU (1) | RU2315053C2 (no) |
| SI (1) | SI1283839T1 (no) |
| SK (1) | SK287748B6 (no) |
| TW (1) | TWI288137B (no) |
| WO (1) | WO2001092264A1 (no) |
| ZA (1) | ZA200208898B (no) |
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| CN101822676A (zh) | 2002-01-28 | 2010-09-08 | 协和发酵麒麟株式会社 | 治疗运动疾病患者的方法 |
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| CN113773327B (zh) * | 2021-09-13 | 2022-07-15 | 八叶草健康产业研究院(厦门)有限公司 | 一种吡唑并嘧啶并三唑环类化合物的制备方法 |
| CN118812544A (zh) * | 2024-06-19 | 2024-10-22 | 厦门大学 | 一种腺苷a2ar靶向小分子化合物、核素标记探针及其制备方法、应用和药物组合物 |
| CN118812539B (zh) * | 2024-06-19 | 2025-11-28 | 苏州大学 | 一种5-氨基三唑并嘧啶衍生物及其制备方法 |
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| EP0217748B1 (en) | 1985-09-30 | 1991-02-06 | Ciba-Geigy Ag | 2-Substituted-e-fused-[1,2,4,]triazolo-[1,5-c]pyrimidines pharmaceutical compositions and uses thereof |
| SU1739850A3 (ru) * | 1987-08-31 | 1992-06-07 | Такеда Кемикал Индастриз, Лтд (Фирма) | Способ получени конденсированных производных пиразоло[3,4- @ ]пиримидина |
| IT1264901B1 (it) | 1993-06-29 | 1996-10-17 | Schering Plough S P A | Analoghi eterociclici di 1,2,4-triazolo(15-c)pirimidine ad attivita' antagonista per il recettore a2 dell'adenosina |
| AU7237294A (en) | 1993-07-27 | 1995-02-28 | Kyowa Hakko Kogyo Co. Ltd. | Remedy for parkinson's disease |
| IT1277392B1 (it) | 1995-07-28 | 1997-11-10 | Schering Plough S P A | Analoghi eterociclici di 1,2,4-triazolo(1,5-c]pirimidine ad attivita' antagonista per il recettore a2a dell'adenosina |
| IT1291372B1 (it) * | 1997-05-21 | 1999-01-07 | Schering Plough S P A | Uso di analoghi eterociclici di 1,2,4-triazolo (1,5-c) pirimidine per la preparazione di medicamenti utili per il trattamento delle malattie |
| AU6808901A (en) * | 2000-05-26 | 2001-12-11 | Schering Corp | Adenosine a2a receptor antagonists |
| MXPA04005209A (es) * | 2001-11-30 | 2004-08-19 | Schering Corp | Antagonistas del receptor de adenosina a2a. |
| EP2269596A3 (en) * | 2002-12-19 | 2011-09-14 | Schering Corporation | Use of adenosine A2a receptor antagonists for the treatment of extrapyramidal syndrome and other movement disorders |
| WO2005044819A1 (en) * | 2003-10-28 | 2005-05-19 | Schering Corporation | Process for preparing substituted 5-amino-pyrazolo-[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines |
| CA2547248A1 (en) * | 2003-12-01 | 2005-06-16 | Schering Corporation | Process for preparing substituted 5-amino-pyrazolo-[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines |
| TW200538118A (en) * | 2004-04-21 | 2005-12-01 | Schering Corp | Pyrazolo-[4,3-e]-1,2,4-triazolo-[1,5-c]-pyrimidine adenosine A2a receptor antagonists |
| ATE538123T1 (de) * | 2005-09-19 | 2012-01-15 | Schering Corp | 2-heteroarylpyrazoloä4,3-eü-1, 2, 4-triazolo-ä1,5-cü-pyrimidine als antagonisten des adenosin-a2a- rezeptors |
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