CN1946725B - 用作细胞周期蛋白依赖激酶抑制剂的新型吡唑并嘧啶 - Google Patents
用作细胞周期蛋白依赖激酶抑制剂的新型吡唑并嘧啶 Download PDFInfo
- Publication number
- CN1946725B CN1946725B CN2005800122934A CN200580012293A CN1946725B CN 1946725 B CN1946725 B CN 1946725B CN 2005800122934 A CN2005800122934 A CN 2005800122934A CN 200580012293 A CN200580012293 A CN 200580012293A CN 1946725 B CN1946725 B CN 1946725B
- Authority
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- China
- Prior art keywords
- compound
- alkyl
- aryl
- mmol
- heteroaryl
- 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 - Lifetime
Links
- 0 C*C(C)C=C(*)CC1N2C=C[C@]2N(*)*C(C)=C1 Chemical compound C*C(C)C=C(*)CC1N2C=C[C@]2N(*)*C(C)=C1 0.000 description 19
- MSYOFDUYFPVPHV-UHFFFAOYSA-N Bc1c2nc(C3CCCCC3)cc(NCc(cc3)ccc3N)[n]2nc1 Chemical compound Bc1c2nc(C3CCCCC3)cc(NCc(cc3)ccc3N)[n]2nc1 MSYOFDUYFPVPHV-UHFFFAOYSA-N 0.000 description 1
- SMIZFGZXFDGISG-UHFFFAOYSA-N Brc(cn[n]1c(NCc2cnccc2)c2)c1nc2-c1ccccc1 Chemical compound Brc(cn[n]1c(NCc2cnccc2)c2)c1nc2-c1ccccc1 SMIZFGZXFDGISG-UHFFFAOYSA-N 0.000 description 1
- RVDPXWNUVFCWCH-WNNGRJQASA-N C/C=C/C(/CNc([n]1nc2)cc(-c(cccc3)c3Cl)nc1c2Br)=C\C=C/NOC Chemical compound C/C=C/C(/CNc([n]1nc2)cc(-c(cccc3)c3Cl)nc1c2Br)=C\C=C/NOC RVDPXWNUVFCWCH-WNNGRJQASA-N 0.000 description 1
- IQJZUYFOSMJZSV-ZETCQYMHSA-N CC(C)(C)[C@H]1NCCC1 Chemical compound CC(C)(C)[C@H]1NCCC1 IQJZUYFOSMJZSV-ZETCQYMHSA-N 0.000 description 1
- KRIOVPPHQSLHCZ-UHFFFAOYSA-N CCC(c1ccccc1)=O Chemical compound CCC(c1ccccc1)=O KRIOVPPHQSLHCZ-UHFFFAOYSA-N 0.000 description 1
- BMLMXLRJGCBOOF-SSDOTTSWSA-N C[C@H](CC1)CC1=C Chemical compound C[C@H](CC1)CC1=C BMLMXLRJGCBOOF-SSDOTTSWSA-N 0.000 description 1
- RGXUCUWVGKLACF-UHFFFAOYSA-N Cc1cc(CN)ccc1 Chemical compound Cc1cc(CN)ccc1 RGXUCUWVGKLACF-UHFFFAOYSA-N 0.000 description 1
- KVSIJRIBZQPYQR-UHFFFAOYSA-N Clc(cccc1)c1-c(cc(NCc1cnccc1)[n]1nc2)nc1c2Br Chemical compound Clc(cccc1)c1-c(cc(NCc1cnccc1)[n]1nc2)nc1c2Br KVSIJRIBZQPYQR-UHFFFAOYSA-N 0.000 description 1
- XBPWUNNYJOLFGX-UHFFFAOYSA-N NC(CCC1)C1=O Chemical compound NC(CCC1)C1=O XBPWUNNYJOLFGX-UHFFFAOYSA-N 0.000 description 1
- SBMSLRMNBSMKQC-UHFFFAOYSA-N NN1CCCC1 Chemical compound NN1CCCC1 SBMSLRMNBSMKQC-UHFFFAOYSA-N 0.000 description 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
- C07D487/02—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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Oncology (AREA)
- Neurology (AREA)
- Rheumatology (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Pain & Pain Management (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/776,988 | 2004-02-11 | ||
| US10/776,988 US7119200B2 (en) | 2002-09-04 | 2004-02-11 | Pyrazolopyrimidines as cyclin dependent kinase inhibitors |
| PCT/US2005/003859 WO2005077954A2 (en) | 2004-02-11 | 2005-02-08 | Pyrazolopyrimidine-derivatives as cyclin dependent kinase inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1946725A CN1946725A (zh) | 2007-04-11 |
| CN1946725B true CN1946725B (zh) | 2011-02-23 |
Family
ID=34860861
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2005800122934A Expired - Lifetime CN1946725B (zh) | 2004-02-11 | 2005-02-08 | 用作细胞周期蛋白依赖激酶抑制剂的新型吡唑并嘧啶 |
Country Status (26)
| Country | Link |
|---|---|
| US (2) | US7119200B2 (enExample) |
| EP (1) | EP1720882B1 (enExample) |
| JP (2) | JP4845743B2 (enExample) |
| KR (1) | KR101196498B1 (enExample) |
| CN (1) | CN1946725B (enExample) |
| AR (1) | AR047543A1 (enExample) |
| AT (1) | ATE494287T1 (enExample) |
| AU (1) | AU2005212409C1 (enExample) |
| BR (1) | BRPI0507644B8 (enExample) |
| CA (1) | CA2555345C (enExample) |
| CY (1) | CY1112400T1 (enExample) |
| DE (1) | DE602005025733D1 (enExample) |
| DK (1) | DK1720882T3 (enExample) |
| ES (1) | ES2359410T3 (enExample) |
| HR (1) | HRP20110245T1 (enExample) |
| IL (1) | IL177283A (enExample) |
| MY (1) | MY149044A (enExample) |
| NO (1) | NO337520B1 (enExample) |
| NZ (1) | NZ590480A (enExample) |
| PE (1) | PE20050774A1 (enExample) |
| PL (1) | PL1720882T3 (enExample) |
| RU (1) | RU2414472C9 (enExample) |
| SI (1) | SI1720882T1 (enExample) |
| TW (1) | TWI393566B (enExample) |
| WO (1) | WO2005077954A2 (enExample) |
| ZA (1) | ZA200606573B (enExample) |
Families Citing this family (116)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US7196092B2 (en) * | 2002-09-04 | 2007-03-27 | Schering Corporation | N-heteroaryl pyrazolopyrimidines as cyclin dependent kinase inhibitors |
| US7196078B2 (en) * | 2002-09-04 | 2007-03-27 | Schering Corpoartion | Trisubstituted and tetrasubstituted pyrazolopyrimidines as cyclin dependent kinase inhibitors |
| US7119200B2 (en) * | 2002-09-04 | 2006-10-10 | Schering Corporation | Pyrazolopyrimidines as cyclin dependent kinase inhibitors |
| BRPI0407834A (pt) * | 2003-02-28 | 2006-02-14 | Teijin Pharma Ltd | composto, processo para a manufatura do mesmo, composição, processo para a manufatura da mesma, método de tratamento ou prevenção de um distúrbio mediado por proteìna quinase em um indivìduo, uso de um composto, ensaio para determinar a atividade dos compostos, e, método de inibição da atividade ou função de uma proteìna quinase |
| WO2004087707A1 (en) * | 2003-03-31 | 2004-10-14 | Vernalis (Cambridge) Limited | Pyrazolopyrimidine compounds and their use in medicine |
| GB0321475D0 (en) * | 2003-09-12 | 2003-10-15 | Glaxo Group Ltd | Novel compounds |
| WO2005035516A1 (ja) * | 2003-10-10 | 2005-04-21 | Ono Pharmaceutical Co., Ltd. | 新規縮合複素環化合物およびその用途 |
| JP2007536369A (ja) * | 2004-05-06 | 2007-12-13 | ファイザー・インク | プロリン及びモルホリン誘導体の新規化合物 |
| US20080287405A1 (en) * | 2004-05-14 | 2008-11-20 | Thannickal Victor J | Compositions and Methods Relating to Protein Kinase Inhibitors |
| RU2006146985A (ru) * | 2004-05-28 | 2008-07-10 | Вертекс Фармасьютикалз Инкорпорейтед (Us) | Модуляторы мускариновых рецепторов |
| AR051966A1 (es) * | 2004-11-23 | 2007-02-21 | Astrazeneca Ab | Derivados de acido fenoxiacetico utiles para el tratamiento de enfermedades respiratorias |
| US7850960B2 (en) * | 2004-12-30 | 2010-12-14 | University Of Washington | Methods for regulation of stem cells |
| CN101193865A (zh) | 2005-06-09 | 2008-06-04 | 先灵公司 | 3-氨基-4-取代吡唑衍生物的合成 |
| JP2009502801A (ja) * | 2005-07-22 | 2009-01-29 | サネシス ファーマシューティカルズ, インコーポレイテッド | Auroraキナーゼインヒビターとして有用なピラゾロピリミジン |
| EP1922321A1 (en) * | 2005-08-09 | 2008-05-21 | Eirx Therapeutics Ltd | Pyrazoloý1,5-a¨pyrimidine compounds and pharmaceutical compositions containing them |
| BRPI0616985B1 (pt) * | 2005-10-06 | 2021-10-26 | Merck Sharp & Dohme Corp. | Composto de pirazolo[1,5-a]pirimidina, e, uso de um composto |
| US7671221B2 (en) * | 2005-12-28 | 2010-03-02 | Vertex Pharmaceuticals Incorporated | Modulators of ATP-Binding Cassette transporters |
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| BRPI0708693A2 (pt) * | 2006-03-08 | 2011-06-14 | Novartis Ag | uso de derivados de pirazol[1,5,a]pirimidin-7-il amina no tratamento de distérbios neurolàgicos |
| AU2007268083A1 (en) * | 2006-05-22 | 2007-12-06 | Schering Corporation | Pyrazolo [1, 5-A] pyrimidines as CDK inhibitors |
| EP2405270B1 (en) | 2006-06-30 | 2013-07-17 | Merck Sharp & Dohme Corp. | IGFBP2-Biomarker |
| US7786306B2 (en) * | 2006-08-18 | 2010-08-31 | Schering Corporation | Process for resolving chiral piperidine alcohol and process for synthesis of pyrazolo[1,5-a] pyrimidine derivatives using same |
| EP2051963B1 (en) * | 2006-08-18 | 2012-05-16 | Schering Corporation | Process for resolving chiral piperidine alcohol and process for synthesis of pyrazolo [1,5-a]pyrimidine derivatives using same |
| ES2685837T3 (es) * | 2006-08-28 | 2018-10-11 | Merck Sharp & Dohme Corp. | Proceso y productos intermedios para la síntesis de derivados de (3-alquil-5-piperidin-1-il-3,3a-dihidropirazolo[1,5-a]pirimidin-7-il)-amino |
| CN101627041A (zh) * | 2006-08-28 | 2010-01-13 | 先灵公司 | 合成(3-烷基-5-哌啶-1-基-3,3a-二氢-吡唑并[1,5-a]嘧啶-7-基)-氨基衍生物和中间体的方法和中间体 |
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| AU2008261027A1 (en) * | 2007-06-05 | 2008-12-11 | Emory University | Selective inhibitors for cyclin-dependent kinases |
| WO2009020140A1 (ja) * | 2007-08-06 | 2009-02-12 | Dainippon Sumitomo Pharma Co., Ltd. | アダマンチルウレア誘導体 |
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