CN102066338A - 蛋白激酶抑制剂 - Google Patents
蛋白激酶抑制剂 Download PDFInfo
- Publication number
- CN102066338A CN102066338A CN2009801223945A CN200980122394A CN102066338A CN 102066338 A CN102066338 A CN 102066338A CN 2009801223945 A CN2009801223945 A CN 2009801223945A CN 200980122394 A CN200980122394 A CN 200980122394A CN 102066338 A CN102066338 A CN 102066338A
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- China
- Prior art keywords
- alkylene
- ylamino
- pyrrolo
- pyrimidin
- compound
- 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.)
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- 0 CCN(CCNC)c(cc1)ccc1Nc1nc(N)c(c(*)c[n]2)c2n1 Chemical compound CCN(CCNC)c(cc1)ccc1Nc1nc(N)c(c(*)c[n]2)c2n1 0.000 description 11
- XTSZOIFGYJPKJD-UVTDQMKNSA-N C/C(/C1CC1)=C(/Nc1cccc(CN)c1)\N=C Chemical compound C/C(/C1CC1)=C(/Nc1cccc(CN)c1)\N=C XTSZOIFGYJPKJD-UVTDQMKNSA-N 0.000 description 1
- AATNTJMCHYXVNG-VOTSOKGWSA-N C/C(/N(C)C(C)=O)=C\C=C Chemical compound C/C(/N(C)C(C)=O)=C\C=C AATNTJMCHYXVNG-VOTSOKGWSA-N 0.000 description 1
- GLUUGHFHXGJENI-UHFFFAOYSA-N C1NCCNC1 Chemical compound C1NCCNC1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 1
- LSOZALWRNWQPLK-UHFFFAOYSA-N CC(C)(C)OC(NCc1cccc(N)c1)=O Chemical compound CC(C)(C)OC(NCc1cccc(N)c1)=O LSOZALWRNWQPLK-UHFFFAOYSA-N 0.000 description 1
- DTWBXDPKBINBPU-WUKNDPDISA-N CC(C)=N/C(/Nc1cccc(CN)c1)=C(/C=CC1)\C1=C Chemical compound CC(C)=N/C(/Nc1cccc(CN)c1)=C(/C=CC1)\C1=C DTWBXDPKBINBPU-WUKNDPDISA-N 0.000 description 1
- QFELUFGHFLYZEZ-UHFFFAOYSA-N CC(N(C)c(cc1)ccc1N)=O Chemical compound CC(N(C)c(cc1)ccc1N)=O QFELUFGHFLYZEZ-UHFFFAOYSA-N 0.000 description 1
- KQWAZUIXOLONSF-WAYWQWQTSA-N CC(NCCNC(/C=C\C(Nc1nc(N)c(cc[nH]2)c2n1)=C)=C)=C Chemical compound CC(NCCNC(/C=C\C(Nc1nc(N)c(cc[nH]2)c2n1)=C)=C)=C KQWAZUIXOLONSF-WAYWQWQTSA-N 0.000 description 1
- NAJHROHCNMHJFN-SOFYXZRVSA-N CCC(C)Nc(nc(N(CC)/N=C\C)nc1)c1C(N)=O Chemical compound CCC(C)Nc(nc(N(CC)/N=C\C)nc1)c1C(N)=O NAJHROHCNMHJFN-SOFYXZRVSA-N 0.000 description 1
- QUEADLCOKFPJKC-UHFFFAOYSA-N CCC(C)Nc1c(cc[nH]2)c2nc(Nc2cc(CS(C)(O)=O)ccc2)n1 Chemical compound CCC(C)Nc1c(cc[nH]2)c2nc(Nc2cc(CS(C)(O)=O)ccc2)n1 QUEADLCOKFPJKC-UHFFFAOYSA-N 0.000 description 1
- REKFCYNAMPLYIX-UHFFFAOYSA-N CCN(CC)c1c(cc[nH]2)c2nc(Nc(cc2)cc(CC3)c2NC3=O)n1 Chemical compound CCN(CC)c1c(cc[nH]2)c2nc(Nc(cc2)cc(CC3)c2NC3=O)n1 REKFCYNAMPLYIX-UHFFFAOYSA-N 0.000 description 1
- ZTBANHKCVVIBSN-UHFFFAOYSA-N CCc1cc(Nc2c(cc[n]3S(c4ccc(C)cc4)(=O)=O)c3nc(Cl)n2)ccc1 Chemical compound CCc1cc(Nc2c(cc[n]3S(c4ccc(C)cc4)(=O)=O)c3nc(Cl)n2)ccc1 ZTBANHKCVVIBSN-UHFFFAOYSA-N 0.000 description 1
- PTGIFVXPXSRWDR-UHFFFAOYSA-N CN(C)C(C(CC1)CCN1c(cc1)ccc1Nc1nc(NC2CC2)c(cc[nH]2)c2n1)=O Chemical compound CN(C)C(C(CC1)CCN1c(cc1)ccc1Nc1nc(NC2CC2)c(cc[nH]2)c2n1)=O PTGIFVXPXSRWDR-UHFFFAOYSA-N 0.000 description 1
- FDMGNGOLNHZFRH-UHFFFAOYSA-N Nc1c(C=C[U]2)c2cc(I)n1 Chemical compound Nc1c(C=C[U]2)c2cc(I)n1 FDMGNGOLNHZFRH-UHFFFAOYSA-N 0.000 description 1
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- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
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- C—CHEMISTRY; METALLURGY
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
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- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D473/16—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two nitrogen atoms
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
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- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
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- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Diabetes (AREA)
- Heart & Thoracic Surgery (AREA)
- Pulmonology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Obesity (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pain & Pain Management (AREA)
- Hospice & Palliative Care (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Oncology (AREA)
- Physical Education & Sports Medicine (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US4707708P | 2008-04-22 | 2008-04-22 | |
| US61/047,077 | 2008-04-22 | ||
| PCT/US2009/002512 WO2009131687A2 (en) | 2008-04-22 | 2009-04-22 | Inhibitors of protein kinases |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2013100825419A Division CN103224497A (zh) | 2008-04-22 | 2009-04-22 | 蛋白激酶抑制剂 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN102066338A true CN102066338A (zh) | 2011-05-18 |
Family
ID=40910850
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2009801223945A Pending CN102066338A (zh) | 2008-04-22 | 2009-04-22 | 蛋白激酶抑制剂 |
| CN2013100825419A Pending CN103224497A (zh) | 2008-04-22 | 2009-04-22 | 蛋白激酶抑制剂 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2013100825419A Pending CN103224497A (zh) | 2008-04-22 | 2009-04-22 | 蛋白激酶抑制剂 |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US8258144B2 (enExample) |
| EP (1) | EP2271631B1 (enExample) |
| JP (1) | JP2011518219A (enExample) |
| CN (2) | CN102066338A (enExample) |
| AU (1) | AU2009238590A1 (enExample) |
| BR (1) | BRPI0910668A2 (enExample) |
| CA (1) | CA2723185A1 (enExample) |
| IL (1) | IL208719A0 (enExample) |
| NZ (1) | NZ588830A (enExample) |
| WO (1) | WO2009131687A2 (enExample) |
Cited By (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104177363A (zh) * | 2013-05-24 | 2014-12-03 | 江苏先声药物研究有限公司 | 双环杂环胺类Hedgehog信号通路抑制剂 |
| CN105188704A (zh) * | 2013-01-16 | 2015-12-23 | 西格诺药品有限公司 | 被取代的吡咯并嘧啶化合物、其组合物和使用其的治疗方法 |
| CN105837577A (zh) * | 2015-02-02 | 2016-08-10 | 四川大学 | 1-(嘧啶-4-基)3-胺基哌啶衍生物及其制备方法和用途 |
| CN106132934A (zh) * | 2014-01-23 | 2016-11-16 | 加拉帕戈斯股份有限公司 | 治疗炎性病症的苯并咪唑衍生物及其医药组合物 |
| CN106187899A (zh) * | 2016-06-28 | 2016-12-07 | 绍兴文理学院 | 一种氟代氮杂芳烃的合成方法 |
| CN106349224A (zh) * | 2016-08-03 | 2017-01-25 | 山东大学 | 一种含有4‑氨基‑(1h)‑吡唑结构的jak激酶抑制剂及其制备方法和应用 |
| CN107531725A (zh) * | 2015-08-13 | 2018-01-02 | 北京韩美药品有限公司 | Irak4抑制剂及其应用 |
| CN107709327A (zh) * | 2015-06-22 | 2018-02-16 | 小野药品工业株式会社 | Brk抑制性化合物 |
| CN108137559A (zh) * | 2015-07-09 | 2018-06-08 | 默克专利有限公司 | 用作btk抑制剂的嘧啶衍生物及其用途 |
| CN109311896A (zh) * | 2016-06-30 | 2019-02-05 | 株式会社大熊制药 | 吡唑并嘧啶衍生物作为激酶抑制剂 |
| CN111423384A (zh) * | 2019-07-04 | 2020-07-17 | 沈阳药科大学 | 2-氨基嘧啶类化合物及其用途 |
| CN111527091A (zh) * | 2017-12-28 | 2020-08-11 | 株式会社大熊制药 | 作为激酶抑制剂的氧基-氟哌啶衍生物 |
| CN111892580A (zh) * | 2020-09-29 | 2020-11-06 | 北京鑫开元医药科技有限公司 | 一种2-氨基-4-(异吲哚啉-2-基)嘧啶-5-甲酰胺衍生物、制备方法及应用 |
| CN112107580A (zh) * | 2020-09-29 | 2020-12-22 | 北京鑫开元医药科技有限公司 | 一种脾酪氨酸激酶抑制剂的制剂组合物及其制备方法 |
| CN113557237A (zh) * | 2019-01-18 | 2021-10-26 | 沃若诺伊公司 | 吡咯并吡啶衍生物及其预防或治疗蛋白激酶相关疾病的用途 |
| CN113717194A (zh) * | 2020-05-25 | 2021-11-30 | 上海翰森生物医药科技有限公司 | 杂芳类衍生物的盐及其制备方法 |
| CN113717202A (zh) * | 2020-05-25 | 2021-11-30 | 上海翰森生物医药科技有限公司 | 杂芳类衍生物的自由碱晶型及其制备方法 |
| WO2021238908A1 (zh) * | 2020-05-25 | 2021-12-02 | 上海翰森生物医药科技有限公司 | 杂芳类衍生物的盐、晶型及其制备方法 |
| WO2022228511A1 (zh) * | 2021-04-30 | 2022-11-03 | 微境生物医药科技(上海)有限公司 | 作为Wee-1抑制剂的稠环化合物及其制备方法和用途 |
| WO2024099229A1 (zh) * | 2022-11-09 | 2024-05-16 | 沈阳药科大学 | 2-氨基嘧啶类化合物及其用途 |
Families Citing this family (151)
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| CN115667228A (zh) * | 2020-05-25 | 2023-01-31 | 上海翰森生物医药科技有限公司 | 杂芳类衍生物的盐、晶型及其制备方法 |
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| CN112107580A (zh) * | 2020-09-29 | 2020-12-22 | 北京鑫开元医药科技有限公司 | 一种脾酪氨酸激酶抑制剂的制剂组合物及其制备方法 |
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| WO2022228511A1 (zh) * | 2021-04-30 | 2022-11-03 | 微境生物医药科技(上海)有限公司 | 作为Wee-1抑制剂的稠环化合物及其制备方法和用途 |
| CN117222648A (zh) * | 2021-04-30 | 2023-12-12 | 微境生物医药科技(上海)有限公司 | 作为Wee-1抑制剂的稠环化合物及其制备方法和用途 |
| WO2024099229A1 (zh) * | 2022-11-09 | 2024-05-16 | 沈阳药科大学 | 2-氨基嘧啶类化合物及其用途 |
Also Published As
| Publication number | Publication date |
|---|---|
| US20130029944A1 (en) | 2013-01-31 |
| NZ588830A (en) | 2012-11-30 |
| IL208719A0 (en) | 2010-12-30 |
| US8258144B2 (en) | 2012-09-04 |
| US9139581B2 (en) | 2015-09-22 |
| WO2009131687A2 (en) | 2009-10-29 |
| AU2009238590A1 (en) | 2009-10-29 |
| US20090298823A1 (en) | 2009-12-03 |
| BRPI0910668A2 (pt) | 2019-09-24 |
| EP2271631A2 (en) | 2011-01-12 |
| JP2011518219A (ja) | 2011-06-23 |
| CA2723185A1 (en) | 2009-10-29 |
| CN103224497A (zh) | 2013-07-31 |
| WO2009131687A3 (en) | 2010-01-07 |
| EP2271631B1 (en) | 2018-07-04 |
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