CN115697993A - 作为axl抑制剂的嘧啶类化合物 - Google Patents
作为axl抑制剂的嘧啶类化合物 Download PDFInfo
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- CN115697993A CN115697993A CN202180039152.0A CN202180039152A CN115697993A CN 115697993 A CN115697993 A CN 115697993A CN 202180039152 A CN202180039152 A CN 202180039152A CN 115697993 A CN115697993 A CN 115697993A
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- 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
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
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- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
- C07F9/65583—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
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- C07F9/65586—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system at least one of the hetero rings does not contain nitrogen as ring hetero atom
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
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Abstract
本发明公开了作为AXL抑制剂的嘧啶类化合物,该嘧啶类化合物的结构如通式I所示,各取代基的定义如说明书所述,本发明还提供了其制备方法。本发明的嘧啶类化合物具有显著的AXL抑制活性,能够用作AXL抑制剂。
Description
PCT国内申请,说明书已公开。
Claims (14)
- PCT国内申请,权利要求书已公开。
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202010471712 | 2020-05-29 | ||
CN2020104717127 | 2020-05-29 | ||
CN202110003579 | 2021-01-04 | ||
CN2021100035797 | 2021-01-04 | ||
PCT/CN2021/096942 WO2021239133A1 (zh) | 2020-05-29 | 2021-05-28 | 作为axl抑制剂的嘧啶类化合物 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN115697993A true CN115697993A (zh) | 2023-02-03 |
CN115697993B CN115697993B (zh) | 2024-12-10 |
Family
ID=78723011
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202180039152.0A Active CN115697993B (zh) | 2020-05-29 | 2021-05-28 | 作为axl抑制剂的嘧啶类化合物 |
Country Status (7)
Country | Link |
---|---|
US (1) | US20230227484A1 (zh) |
EP (1) | EP4163278A4 (zh) |
JP (1) | JP2023527242A (zh) |
CN (1) | CN115697993B (zh) |
AU (1) | AU2021280113B2 (zh) |
CA (1) | CA3180623A1 (zh) |
WO (1) | WO2021239133A1 (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2024199100A1 (zh) * | 2023-03-24 | 2024-10-03 | 南京正大天晴制药有限公司 | 一种axl抑制剂中间体的制备方法 |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP4277902A4 (en) * | 2021-01-07 | 2024-12-18 | Ontario Institute for Cancer Research (OICR) | ISOINDOLINONE-AMINOPYRIMIDINE COMPOUNDS AS INHIBITORS OF NUAK KINASES, COMPOSITIONS AND USES THEREOF |
CN115838383A (zh) * | 2021-09-22 | 2023-03-24 | 南京正大天晴制药有限公司 | 作为axl抑制剂的苯并环庚烷类化合物 |
CN116178433A (zh) * | 2021-11-26 | 2023-05-30 | 南京正大天晴制药有限公司 | Axl激酶抑制剂的盐及其制备方法和用途 |
CN116178434A (zh) * | 2021-11-26 | 2023-05-30 | 南京正大天晴制药有限公司 | Axl激酶抑制剂的单对甲苯磺酸盐及其晶型 |
AR129722A1 (es) | 2022-06-28 | 2024-09-18 | Arcus Biosciences Inc | Compuestos inhibidores de axl |
WO2024141040A1 (zh) * | 2022-12-30 | 2024-07-04 | 南京正大天晴制药有限公司 | 作为axl抑制剂的药物组合物 |
WO2024199102A1 (zh) * | 2023-03-24 | 2024-10-03 | 南京正大天晴制药有限公司 | 一种axl抑制剂的制备方法 |
WO2024206858A1 (en) | 2023-03-30 | 2024-10-03 | Revolution Medicines, Inc. | Compositions for inducing ras gtp hydrolysis and uses thereof |
WO2024229406A1 (en) | 2023-05-04 | 2024-11-07 | Revolution Medicines, Inc. | Combination therapy for a ras related disease or disorder |
US20250049810A1 (en) | 2023-08-07 | 2025-02-13 | Revolution Medicines, Inc. | Methods of treating a ras protein-related disease or disorder |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101535276A (zh) * | 2006-10-23 | 2009-09-16 | 赛福伦公司 | 作为ALK和c-MET抑制剂的2,4-二氨基嘧啶稠合双环衍生物 |
CN101796046A (zh) * | 2007-07-16 | 2010-08-04 | 阿斯利康(瑞典)有限公司 | 嘧啶衍生物934 |
CN102356075A (zh) * | 2009-01-23 | 2012-02-15 | 里格尔药品股份有限公司 | 抑制jak途径的组合物和方法 |
CN103201280A (zh) * | 2010-07-28 | 2013-07-10 | 里格尔药品股份有限公司 | 抑制jak途径的组合物和方法 |
WO2013173506A2 (en) * | 2012-05-16 | 2013-11-21 | Rigel Pharmaceuticals, Inc. | Method of treating muscular degradation |
CN106458914A (zh) * | 2014-03-28 | 2017-02-22 | 常州捷凯医药科技有限公司 | 作为axl抑制剂的杂环化合物 |
WO2018102366A1 (en) * | 2016-11-30 | 2018-06-07 | Ariad Pharmaceuticals, Inc. | Anilinopyrimidines as haematopoietic progenitor kinase 1 (hpk1) inhibitors |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5592884B2 (ja) * | 2008-07-09 | 2014-09-17 | ライジェル ファーマシューティカルズ, インコーポレイテッド | Axl阻害剤として有用な多環式ヘテロアリール置換トリアゾール |
EP3159338A4 (en) * | 2014-06-17 | 2018-01-24 | Korea Research Institute of Chemical Technology | Pyrimidine-2,4-diamine derivative and anticancer pharmaceutical composition comprising same as effective ingredient |
-
2021
- 2021-05-28 US US17/928,612 patent/US20230227484A1/en active Pending
- 2021-05-28 CN CN202180039152.0A patent/CN115697993B/zh active Active
- 2021-05-28 AU AU2021280113A patent/AU2021280113B2/en active Active
- 2021-05-28 EP EP21811893.3A patent/EP4163278A4/en active Pending
- 2021-05-28 WO PCT/CN2021/096942 patent/WO2021239133A1/zh unknown
- 2021-05-28 JP JP2022573620A patent/JP2023527242A/ja active Pending
- 2021-05-28 CA CA3180623A patent/CA3180623A1/en active Pending
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101535276A (zh) * | 2006-10-23 | 2009-09-16 | 赛福伦公司 | 作为ALK和c-MET抑制剂的2,4-二氨基嘧啶稠合双环衍生物 |
CN101796046A (zh) * | 2007-07-16 | 2010-08-04 | 阿斯利康(瑞典)有限公司 | 嘧啶衍生物934 |
CN102356075A (zh) * | 2009-01-23 | 2012-02-15 | 里格尔药品股份有限公司 | 抑制jak途径的组合物和方法 |
CN103201280A (zh) * | 2010-07-28 | 2013-07-10 | 里格尔药品股份有限公司 | 抑制jak途径的组合物和方法 |
WO2013173506A2 (en) * | 2012-05-16 | 2013-11-21 | Rigel Pharmaceuticals, Inc. | Method of treating muscular degradation |
CN106458914A (zh) * | 2014-03-28 | 2017-02-22 | 常州捷凯医药科技有限公司 | 作为axl抑制剂的杂环化合物 |
WO2018102366A1 (en) * | 2016-11-30 | 2018-06-07 | Ariad Pharmaceuticals, Inc. | Anilinopyrimidines as haematopoietic progenitor kinase 1 (hpk1) inhibitors |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2024199100A1 (zh) * | 2023-03-24 | 2024-10-03 | 南京正大天晴制药有限公司 | 一种axl抑制剂中间体的制备方法 |
Also Published As
Publication number | Publication date |
---|---|
JP2023527242A (ja) | 2023-06-27 |
AU2021280113A8 (en) | 2023-02-23 |
AU2021280113B2 (en) | 2023-12-21 |
EP4163278A1 (en) | 2023-04-12 |
EP4163278A4 (en) | 2024-07-17 |
CN115697993B (zh) | 2024-12-10 |
WO2021239133A1 (zh) | 2021-12-02 |
CA3180623A1 (en) | 2021-12-02 |
AU2021280113A1 (en) | 2023-02-09 |
US20230227484A1 (en) | 2023-07-20 |
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