WO2026087635A1 - Dérivés de dihydrobenzoxazine - Google Patents
Dérivés de dihydrobenzoxazineInfo
- Publication number
- WO2026087635A1 WO2026087635A1 PCT/EP2025/080568 EP2025080568W WO2026087635A1 WO 2026087635 A1 WO2026087635 A1 WO 2026087635A1 EP 2025080568 W EP2025080568 W EP 2025080568W WO 2026087635 A1 WO2026087635 A1 WO 2026087635A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- phenyl
- trifluoromethyl
- chloro
- thia
- dione
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/08—Bridged systems
-
- 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
-
- 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
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
- C07D513/18—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D515/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D515/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D515/08—Bridged systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
L'invention concerne de nouveaux composés hétérocycliques de formule générale (I) dans laquelle A, R1, R2, R3, R4, R5, R6, RA1, RA2 et L sont tels que définis dans la description, des compositions comprenant les composés et des procédés d'utilisation des composés.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP24208558 | 2024-10-24 | ||
| EP24208558.7 | 2024-10-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2026087635A1 true WO2026087635A1 (fr) | 2026-04-30 |
Family
ID=93284471
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP2025/080568 Pending WO2026087635A1 (fr) | 2024-10-24 | 2025-10-23 | Dérivés de dihydrobenzoxazine |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2026087635A1 (fr) |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2015171610A2 (fr) * | 2014-05-05 | 2015-11-12 | Lycera Corporation | Sulfonamide de tétrahydroquinoline et composés apparentés destinés à servir d'agonistes de rory et pour le traitement de maladies |
| WO2017040963A1 (fr) * | 2015-09-03 | 2017-03-09 | Forma Therapeutics, Inc. | Inhibiteurs de hdac8 bicyclique [6,6] fusionnée |
| WO2023179600A1 (fr) * | 2022-03-21 | 2023-09-28 | 杭州德睿智药科技有限公司 | Nouveaux composés macrohétérocycliques substitués et leur utilisation |
-
2025
- 2025-10-23 WO PCT/EP2025/080568 patent/WO2026087635A1/fr active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2015171610A2 (fr) * | 2014-05-05 | 2015-11-12 | Lycera Corporation | Sulfonamide de tétrahydroquinoline et composés apparentés destinés à servir d'agonistes de rory et pour le traitement de maladies |
| WO2017040963A1 (fr) * | 2015-09-03 | 2017-03-09 | Forma Therapeutics, Inc. | Inhibiteurs de hdac8 bicyclique [6,6] fusionnée |
| WO2023179600A1 (fr) * | 2022-03-21 | 2023-09-28 | 杭州德睿智药科技有限公司 | Nouveaux composés macrohétérocycliques substitués et leur utilisation |
Non-Patent Citations (22)
| Title |
|---|
| "Boronic Acids - Preparation and Applications in Organic Synthesis and Medicine", 2005, JOHN WILEY & SONS |
| "Reductive alkylation - Preparation of Amines", CATALYTIC HYDROGENATION OVER PLATINUM METALS, pages 291 - 303 |
| A. SUZUKI, ORGANOMET. CHEM., vol. 576, 1999, pages 147 - 168 |
| A. SUZUKI, PURE APPL. CHEM., vol. 63, 1991, pages 419 - 422 |
| A. SUZUKIN. MIYAURA, CHEM. REV., vol. 95, 1995, pages 2457 - 2483 |
| ANGEWANDTE CHEMIE, vol. 58, 2019, pages 17118 - 17129 |
| BARANYR. B. MERRIFIELD, J. AM. CHEM. SOC., vol. 99, 1977, pages 7363 |
| BORCHBERNSTEIN, J. AM. CHEM. SOC, vol. 93, 1971, pages 2897 |
| BROWN, H. C.KRISHNAMURTHY, S.: "Selective Reductions. 20. Borane-Methyl Sulfide: A Highly Convenient, Stable, and Selective Reagent for the Reduction of Representative Organic Compounds", J. AM. CHEM. SOC., vol. 94, 1972, pages 7159 - 7161 |
| CHEM. REV., vol. 109, no. 6, 2009, pages 2551 |
| CHEM. SOC. REV., vol. 40, 2011, pages 5084 |
| H. WALDMANN ET AL., ANGEW. CHEM. INT. ED. ENGL., vol. 35, 1996, pages 2056 |
| HECK, R. F.: "The Palladium-Catalyzed Arylation of Enol Esters, Halides, and Dienes", JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, vol. 90, no. 20, 1968, pages 5518 - 5526 |
| JOURNAL OF MEDICINAL CHEMISTRY, vol. 56, no. 10, 2013, pages 3980 - 3995 |
| no. 1203566-77-1 |
| ORG. CHEM. FRONT., vol. 2, 2015, pages 739 |
| ORG. LETT., vol. 20, 2018, pages 4218 - 4222 |
| R.H. GRUBBS, S. MILLER, G.C. FU, ACC. CHEM. RES., vol. 28, 1995, pages 446 - 452 |
| SPENCER JONATHAN A. ET AL: "Design and Development of a Macrocyclic Series Targeting Phosphoinositide 3-Kinase [delta]", ACS MEDICINAL CHEMISTRY LETTERS, vol. 11, no. 7, 3 June 2020 (2020-06-03), US, pages 1386 - 1391, XP093287996, ISSN: 1948-5875, DOI: 10.1021/acsmedchemlett.0c00061 * |
| T. W. GREENEP. G. M. WUTTS: "Protective Groups in Organic Chemistry", 2006, JOHN WILEY & SONS |
| TANG, T. P.; ELLMAN, J. A.: "The tert- Butanesulfinyl Group: An Ideal Chiral Directing Group and Boc-Surrogate for the Asymmetric Synthesis and Applications of β-Amino Acids", J. ORG. CHEM., vol. 64, 1999, pages 12 - 13, XP000916153, DOI: 10.1021/jo9820824 |
| V. POLSHETTIWAR ET AL., CHEM. SUS. CHEM., vol. 3, 2010, pages 502 - 522 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN117917410A (zh) | pan-KRAS降解剂及其制备方法和应用 | |
| EP3452461B1 (fr) | Pipéridines en tant qu'inhibiteurs de ménine | |
| EP2990405B1 (fr) | Composés diaminopyrimidines deutériés, et compositions pharmaceutiques comprenant ces composés | |
| AU2013312587B2 (en) | Imidazoline derivatives, preparation methods thereof, and their applications in medicine | |
| TW202500146A (zh) | 包含喹唑啉化合物之醫藥組合物 | |
| KR102390276B1 (ko) | 마크로사이클릭 피리미딘 유도체 | |
| TW201938555A (zh) | Kras g12c抑制劑 | |
| US10662173B2 (en) | Indole and pyrrole compounds, a process for their preparation and pharmaceutical compositions containing them | |
| US10689364B2 (en) | Isoindoline or isoquinoline compounds, a process for their preparation and pharmaceutical compositions containing them | |
| KR102455519B1 (ko) | ROS1 저해제로서의 치환된 4,5,6,7-테트라히드로피라졸로[1,5-a]피라진 유도체 및 5,6,7,8-테트라히드로-4H-피라졸로[1,5-a][1,4]디아제핀 유도체 | |
| EA020807B1 (ru) | Соединения пиридина | |
| KR20160140739A (ko) | 마크로사이클릭 피리미딘 유도체 | |
| JP2012518612A (ja) | ガンの治療のための新規なオルトアミノアミド類 | |
| TW202313606A (zh) | 取代的苯基-1h-吡咯并[2,3-c]吡啶衍生物 | |
| JP5249031B2 (ja) | 5−HT2C受容体アゴニストとしての6−N結合型へテロ環置換された2,3,4,5−テトラヒドロ−1H−ベンゾ[d]アゼピン | |
| CN114981270A (zh) | Mll1抑制剂和抗癌剂 | |
| AU2024289347A1 (en) | Nmt inhibitor, and preparation method therefor and use thereof | |
| KR20170095243A (ko) | Pi3kbeta 저해제로서의 헤테로사이클릴 연결된 이미다조피리다진 유도체 | |
| CN1726208A (zh) | E-2-甲氧基-n-( 3-{4-[3-甲基-4-( 6-甲基-吡啶-3-基氧基)-苯基氨基]-喹唑啉-6-基}-烯丙基)-乙酰胺的配合物、其制备方法和用途 | |
| CA3168355A1 (fr) | Derives d'indole macrocycliques en tant qu'inhibiteurs de mcl-1 | |
| WO2021239862A1 (fr) | Dérivés macrocycliques de 7-pyrazol-5-yl-indole utilisés en tant qu'inhibiteurs de mcl-1 | |
| WO2025262003A1 (fr) | Dérivés de dihydro benzoxazine | |
| TW202336017A (zh) | Sos1降解劑及其製備方法和應用 | |
| TW202608891A (zh) | Kras g12d降解劑及其製備方法與應用 | |
| CN121609699A (zh) | 具有smarca2抑制作用的化合物及其用途 |