JP2021527051A - ピラゾロ−ピリミジン−アミノ−シクロアルキル化合物及びその治療的使用 - Google Patents
ピラゾロ−ピリミジン−アミノ−シクロアルキル化合物及びその治療的使用 Download PDFInfo
- Publication number
- JP2021527051A JP2021527051A JP2020567845A JP2020567845A JP2021527051A JP 2021527051 A JP2021527051 A JP 2021527051A JP 2020567845 A JP2020567845 A JP 2020567845A JP 2020567845 A JP2020567845 A JP 2020567845A JP 2021527051 A JP2021527051 A JP 2021527051A
- Authority
- JP
- Japan
- Prior art keywords
- substituted
- unsubstituted
- och
- nhc
- cycloalkyl
- 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
- 0 **[n]1nc(*)c2c1nc(N*C1CC(*)*C1)nc2 Chemical compound **[n]1nc(*)c2c1nc(N*C1CC(*)*C1)nc2 0.000 description 4
- SDMHETGSUCLYTO-UHFFFAOYSA-N CC1(C)OB(c(cc2)cc3c2N=CN(C)C3=O)OC1(C)C Chemical compound CC1(C)OB(c(cc2)cc3c2N=CN(C)C3=O)OC1(C)C SDMHETGSUCLYTO-UHFFFAOYSA-N 0.000 description 1
- QVPWTBZHLOHZFW-UHFFFAOYSA-N CC1(C)OB(c2ccc(-c3nnc(C)[s]3)c(CCC#N)c2)OC1(C)C Chemical compound CC1(C)OB(c2ccc(-c3nnc(C)[s]3)c(CCC#N)c2)OC1(C)C QVPWTBZHLOHZFW-UHFFFAOYSA-N 0.000 description 1
- MCSVSXROESVYLR-UHFFFAOYSA-N CN(C=Nc(c1c2)ccc2Br)C1=O Chemical compound CN(C=Nc(c1c2)ccc2Br)C1=O MCSVSXROESVYLR-UHFFFAOYSA-N 0.000 description 1
- GYVYSEPSZWQODX-YZDLTYHYSA-N COCCNC([C@H](CC1)C/C1=N\c(nc12)ncc1c(Br)n[n]2-c1cc2cccnc2cc1)=O Chemical compound COCCNC([C@H](CC1)C/C1=N\c(nc12)ncc1c(Br)n[n]2-c1cc2cccnc2cc1)=O GYVYSEPSZWQODX-YZDLTYHYSA-N 0.000 description 1
- AUUYRPYIBKKRRI-HUUCEWRRSA-N COCc1n[o]c([C@H](CC2)C[C@@H]2Nc(nc23)ncc2c(Br)n[n]3-c2cc3cccnc3cc2)n1 Chemical compound COCc1n[o]c([C@H](CC2)C[C@@H]2Nc(nc23)ncc2c(Br)n[n]3-c2cc3cccnc3cc2)n1 AUUYRPYIBKKRRI-HUUCEWRRSA-N 0.000 description 1
- UIZPNDULKZZLDH-OYLFLEFRSA-N C[C@@](CC1)(C[C@@H]1Nc(nc12)ncc1c(Br)n[n]2-c1cc(NC(c2nccnc2)=O)ccc1)C(NC)=O Chemical compound C[C@@](CC1)(C[C@@H]1Nc(nc12)ncc1c(Br)n[n]2-c1cc(NC(c2nccnc2)=O)ccc1)C(NC)=O UIZPNDULKZZLDH-OYLFLEFRSA-N 0.000 description 1
- CVHADMKAXLAODG-NSCUQIJASA-N C[C@H](c1cc(-[n](c2nc(N[C@H](CC3)C[C@]3(C)C(NC)=O)ncc22)nc2Br)cc2nccnc12)N Chemical compound C[C@H](c1cc(-[n](c2nc(N[C@H](CC3)C[C@]3(C)C(NC)=O)ncc22)nc2Br)cc2nccnc12)N CVHADMKAXLAODG-NSCUQIJASA-N 0.000 description 1
- FWTAMORHKFENPR-VOIUYBSRSA-N Cc(c1cnc(N[C@H](CC2)C[C@]2(CCC#N)C(N)=O)nc11)n[n]1-c1cc2cccnc2c(F)c1 Chemical compound Cc(c1cnc(N[C@H](CC2)C[C@]2(CCC#N)C(N)=O)nc11)n[n]1-c1cc2cccnc2c(F)c1 FWTAMORHKFENPR-VOIUYBSRSA-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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201862680891P | 2018-06-05 | 2018-06-05 | |
| US62/680,891 | 2018-06-05 | ||
| US201962831006P | 2019-04-08 | 2019-04-08 | |
| US62/831,006 | 2019-04-08 | ||
| PCT/US2019/035462 WO2019236631A1 (en) | 2018-06-05 | 2019-06-04 | Pyrazolo-pyrimidin-amino-cycloalkyl compounds and their therapeutic uses |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2021527051A true JP2021527051A (ja) | 2021-10-11 |
| JPWO2019236631A5 JPWO2019236631A5 (https=) | 2022-06-27 |
| JP2021527051A5 JP2021527051A5 (https=) | 2022-06-27 |
Family
ID=67185700
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020567845A Pending JP2021527051A (ja) | 2018-06-05 | 2019-06-04 | ピラゾロ−ピリミジン−アミノ−シクロアルキル化合物及びその治療的使用 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US11046699B2 (https=) |
| EP (1) | EP3802544A1 (https=) |
| JP (1) | JP2021527051A (https=) |
| TW (1) | TW202016112A (https=) |
| WO (1) | WO2019236631A1 (https=) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111499644B (zh) * | 2020-04-24 | 2021-07-20 | 苏州大学 | 咪唑并[1,5-a]喹唑啉-5(4H)-酮类衍生物及其制备方法和用途 |
| GB202008749D0 (en) | 2020-06-09 | 2020-07-22 | Ip2Ipo Innovations Ltd | Novel compounds |
| WO2022072783A1 (en) | 2020-10-02 | 2022-04-07 | Incyte Corporation | Bicyclic dione compounds as inhibitors of kras |
| CN114516828A (zh) * | 2020-11-19 | 2022-05-20 | 江苏威奇达药业有限公司 | 一种提高负氮杂提取率的提取工艺 |
| US20250000859A1 (en) * | 2021-08-25 | 2025-01-02 | Alesta Therapeutics BV | Use of gcn2 inhibitors in treating cancer |
| WO2023107705A1 (en) | 2021-12-10 | 2023-06-15 | Incyte Corporation | Bicyclic amines as cdk12 inhibitors |
| MX2024007328A (es) | 2021-12-14 | 2024-09-30 | Crossfire Oncology Holding B V | Inhibidores macrociclicos de btk. |
| WO2023110936A1 (en) | 2021-12-14 | 2023-06-22 | Netherlands Translational Research Center Holding B.V | Reversible macrocyclic kinase inhibitors |
| CN116478145B (zh) * | 2022-04-13 | 2024-02-02 | 杭州邦顺制药有限公司 | Alk2激酶抑制剂 |
| UY40234A (es) | 2022-04-22 | 2023-11-15 | Vertex Pharma | Compuestos heteroarilo para el tratamiento del dolor |
| WO2024126617A1 (en) | 2022-12-14 | 2024-06-20 | Crossfire Oncology Holding B.V. | Bifunctional compounds for degrading kinases via ubiquitin proteosome pathway |
| WO2024238570A1 (en) * | 2023-05-15 | 2024-11-21 | Aleksia Therapeutics, Inc. | Cdk2 inhibitor pyrazolopyrimidine compounds |
| CN117756677B (zh) * | 2023-12-21 | 2025-09-30 | 上海馨远医药科技有限公司 | 一种手性反式-n-boc-1-氨基环戊烷-3-甲酸的制备方法 |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005504828A (ja) * | 2001-10-02 | 2005-02-17 | スミスクライン・ビーチャム・コーポレイション | 化合物 |
| JP2010516812A (ja) * | 2007-01-30 | 2010-05-20 | バイオジェン・アイデック・エムエイ・インコーポレイテッド | 有糸分裂キナーゼの調節剤 |
| WO2012098068A1 (en) * | 2011-01-19 | 2012-07-26 | F. Hoffmann-La Roche Ag | Pyrazolo pyrimidines as dyrk1a and dyrk1b inhibitors |
| US20130345268A1 (en) * | 2009-02-13 | 2013-12-26 | The Trustees Of Dartmouth College | Methods and Compositions for the Treatment of RAS Associated Disorders |
| JP2016510044A (ja) * | 2013-03-05 | 2016-04-04 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | 癌などの疾患の処置のためのトリアゾロ[4,5−d]ピリミジン誘導体 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US4911920A (en) | 1986-07-30 | 1990-03-27 | Alcon Laboratories, Inc. | Sustained release, comfort formulation for glaucoma therapy |
| FR2588189B1 (fr) | 1985-10-03 | 1988-12-02 | Merck Sharp & Dohme | Composition pharmaceutique de type a transition de phase liquide-gel |
| ATE141502T1 (de) | 1991-01-15 | 1996-09-15 | Alcon Lab Inc | Verwendung von karrageenan in topischen ophthalmologischen zusammensetzungen |
| US5212162A (en) | 1991-03-27 | 1993-05-18 | Alcon Laboratories, Inc. | Use of combinations gelling polysaccharides and finely divided drug carrier substrates in topical ophthalmic compositions |
| GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
| BR9707495A (pt) | 1996-02-13 | 1999-07-27 | Zeneca Ltd | Derivado de quinazolina processo para a preparação do mesmo composição farmacêutica e processo para a produç o de um efeito antiangiogênico e/ou de redução de permeabilidade vascular em um animal de sangue quente |
| US6291455B1 (en) | 1996-03-05 | 2001-09-18 | Zeneca Limited | 4-anilinoquinazoline derivatives |
| GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
| GB9714249D0 (en) | 1997-07-08 | 1997-09-10 | Angiogene Pharm Ltd | Vascular damaging agents |
| GB9900334D0 (en) | 1999-01-07 | 1999-02-24 | Angiogene Pharm Ltd | Tricylic vascular damaging agents |
| GB9900752D0 (en) | 1999-01-15 | 1999-03-03 | Angiogene Pharm Ltd | Benzimidazole vascular damaging agents |
| NZ522074A (en) | 2000-05-31 | 2004-06-25 | Astrazeneca Ab | Indole derivatives with vascular damaging activity |
| IL153484A0 (en) | 2000-07-07 | 2003-07-06 | Angiogene Pharm Ltd | Colchinol derivatives as angiogenesis inhibitors |
| CN1255392C (zh) | 2000-07-07 | 2006-05-10 | 安吉奥金尼药品有限公司 | 作为血管生成抑制剂的秋水仙醇衍生物 |
| AU2014224976B2 (en) * | 2013-03-05 | 2017-09-28 | Merck Patent Gmbh | 9-(aryl or heteroaryl)-2-(pyrazolyl, pyrrolidinyl or cyclopentyl)aminopurine derivatives as anticancer agents |
-
2019
- 2019-06-04 WO PCT/US2019/035462 patent/WO2019236631A1/en not_active Ceased
- 2019-06-04 US US16/431,504 patent/US11046699B2/en active Active
- 2019-06-04 EP EP19736849.1A patent/EP3802544A1/en not_active Withdrawn
- 2019-06-04 JP JP2020567845A patent/JP2021527051A/ja active Pending
- 2019-06-05 TW TW108119522A patent/TW202016112A/zh unknown
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005504828A (ja) * | 2001-10-02 | 2005-02-17 | スミスクライン・ビーチャム・コーポレイション | 化合物 |
| JP2010516812A (ja) * | 2007-01-30 | 2010-05-20 | バイオジェン・アイデック・エムエイ・インコーポレイテッド | 有糸分裂キナーゼの調節剤 |
| JP2010532312A (ja) * | 2007-01-30 | 2010-10-07 | バイオジェン・アイデック・エムエイ・インコーポレイテッド | 1−h−ピラゾロ(3,4b)ピリミジン誘導体および有糸分裂キナーゼの調節剤としてのその使用 |
| US20130345268A1 (en) * | 2009-02-13 | 2013-12-26 | The Trustees Of Dartmouth College | Methods and Compositions for the Treatment of RAS Associated Disorders |
| WO2012098068A1 (en) * | 2011-01-19 | 2012-07-26 | F. Hoffmann-La Roche Ag | Pyrazolo pyrimidines as dyrk1a and dyrk1b inhibitors |
| JP2016510044A (ja) * | 2013-03-05 | 2016-04-04 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | 癌などの疾患の処置のためのトリアゾロ[4,5−d]ピリミジン誘導体 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2019236631A1 (en) | 2019-12-12 |
| US20190375753A1 (en) | 2019-12-12 |
| TW202016112A (zh) | 2020-05-01 |
| US11046699B2 (en) | 2021-06-29 |
| EP3802544A1 (en) | 2021-04-14 |
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