CR20220068A - Derivados de 2-morfolinopiridina sustituidos como inhibidores de la cinasa atr - Google Patents

Derivados de 2-morfolinopiridina sustituidos como inhibidores de la cinasa atr

Info

Publication number
CR20220068A
CR20220068A CR20220068A CR20220068A CR20220068A CR 20220068 A CR20220068 A CR 20220068A CR 20220068 A CR20220068 A CR 20220068A CR 20220068 A CR20220068 A CR 20220068A CR 20220068 A CR20220068 A CR 20220068A
Authority
CR
Costa Rica
Prior art keywords
optionally substituted
alkyl
substituted
morpholinopyridine
derivatives
Prior art date
Application number
CR20220068A
Other languages
English (en)
Inventor
Abbas Abdoli
Stéphanie Lanoix
Vouy Linh Truong
Sheldon N Crane
Stéphane Dorich
Cameron Black
Jean-François Truchon
Paul Jones
Cyrus M Lacbay
Miguel St-Onge
Lee Fader
Audrey Picard
Original Assignee
Repare Therapeutics Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from PCT/CA2019/051539 external-priority patent/WO2020087170A1/en
Application filed by Repare Therapeutics Inc filed Critical Repare Therapeutics Inc
Publication of CR20220068A publication Critical patent/CR20220068A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic 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)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Se describen compuestos con la fórmula (I) o sales farmacéuticamente aceptables de estos, en donde — es un enlace simple, y cada Y es N o CR4 ; o — está ausente, y cada Y es NRY , carbonilo o (C(RY )2, en donde cada R1 es H o alquilo de C1-6 opcionalmente sustituido; R1 es alquilo de C1-6 opcionalmente sustituido o H; R3 es heteroarilo de C1-9 opcionalmente sustituido o alquilo de C1-6 heteroarilo de C1-9 opcionalmente sustituido; cada R4 es hidrógeno, halógeno, alquilo de C1-6 opcionalmente sustituido, alquenilo de C2-6 opcionalmente sustituido o alquinilo de C2-6 opcionalmente sustituido; X es hidrógeno o halógeno; y R2 es como se define en la reivindicación 1. También se describen composiciones farmacéuticas que contienen los compuestos con la fórmula (I) y métodos para su preparación. Los compuestos con la fórmula (I) pueden ser inhibidores de la proteína cinasa relacionada con ataxia telangiectasia y RAD-3 (ATR) y usarse para el tratamiento de enfermedades y afecciones tales como cánceres.
CR20220068A 2019-07-22 2020-07-22 Derivados de 2-morfolinopiridina sustituidos como inhibidores de la cinasa atr CR20220068A (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201962877177P 2019-07-22 2019-07-22
PCT/CA2019/051539 WO2020087170A1 (en) 2018-10-30 2019-10-30 Compounds, pharmaceutical compositions, and methods of preparing compounds and of their use as atr kinase inhibitors
PCT/CA2020/051014 WO2021012049A1 (en) 2019-07-22 2020-07-22 Substituted 2-morpholinopyridine derivatives as atr kinase inhibitors

Publications (1)

Publication Number Publication Date
CR20220068A true CR20220068A (es) 2022-06-30

Family

ID=74192632

Family Applications (1)

Application Number Title Priority Date Filing Date
CR20220068A CR20220068A (es) 2019-07-22 2020-07-22 Derivados de 2-morfolinopiridina sustituidos como inhibidores de la cinasa atr

Country Status (16)

Country Link
US (1) US20220185809A1 (es)
EP (1) EP4003993A4 (es)
JP (2) JP7617076B2 (es)
KR (1) KR20220035925A (es)
CN (1) CN114174292B (es)
AU (1) AU2020317381A1 (es)
BR (1) BR112022000431A2 (es)
CA (1) CA3148278A1 (es)
CO (1) CO2022001853A2 (es)
CR (1) CR20220068A (es)
EC (1) ECSP22012347A (es)
IL (1) IL289763A (es)
MX (1) MX2022000854A (es)
PH (1) PH12022550156A1 (es)
UA (1) UA129807C2 (es)
WO (1) WO2021012049A1 (es)

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CR20210281A (es) 2018-10-30 2021-10-25 Repare Therapeutics Inc Compuestos, composiciones farmacéuticas y métodos de preparación de compuestos y de uso como inhibidores de la cinasa atr
MX2022000854A (es) * 2019-07-22 2022-02-10 Repare Therapeutics Inc Derivados de 2-morfolinopiridina sustituidos como inhibidores de la cinasa atr.
CA3164203A1 (en) * 2019-12-11 2021-06-17 Repare Therapeutics Inc. Use of atr inhibitors in combination with parp inhibitors
BR112023022481A2 (pt) * 2021-04-28 2024-02-15 Repare Therapeutics Inc Métodos de tratamento de cânceres com mutação de perda de função bialélica ou de superexpressão gênica
MX2023014302A (es) * 2021-06-04 2024-02-28 Repare Therapeutics Inc Formas cristalinas, composiciones que contienen las mismas y métodos para su uso.
KR20240041354A (ko) * 2021-07-27 2024-03-29 릿츠뜨 메디시네스 엘티디 8-옥소-3-아자비시클로[3.2.1]옥탄계 화합물 또는 이의 염 및 이의 제조 방법과 용도
CN113856764B (zh) * 2021-10-29 2022-11-01 华中科技大学 一种过渡金属催化剂及其制备方法和应用
CN116099390B (zh) * 2022-11-14 2024-07-23 石河子大学 一种混合维度材料PNT@NiCo-LDH及其制备方法与应用
WO2024211696A1 (en) * 2023-04-07 2024-10-10 Biogen Ma Inc. 1h-pyrrolo[2,3-b]pyridin-4-yl]-2-oxopyrrolidine-3-carbonitrile derivatives as tyrosine kinase 2 (tyk2) inhibitors for the treatment of inflammatory diseases
AU2024265078A1 (en) 2023-05-04 2025-12-11 Revolution Medicines, Inc. Combination therapy for a ras related disease or disorder
IL326136A (en) 2023-08-07 2026-03-01 Revolution Medicines Inc RMC-6291 for use in the treatment of a disease or disorder associated with the RAS protein
WO2025067111A1 (zh) * 2023-09-27 2025-04-03 苏州必扬医药科技有限公司 一种Menin-MLL相互作用抑制剂及其制备方法和应用
US20250154171A1 (en) 2023-10-12 2025-05-15 Revolution Medicines, Inc. Ras inhibitors
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras inhibitors
WO2025181153A1 (en) * 2024-03-01 2025-09-04 F. Hoffmann-La Roche Ag Use of atr inhibitors in combination with pi3k alpha inhibitors
WO2025217307A1 (en) 2024-04-09 2025-10-16 Revolution Medicines, Inc. Methods for predicting response to a ras(on) inhibitor and combination therapies
TW202545519A (zh) * 2024-05-15 2025-12-01 俄羅斯聯邦商拜奧卡德聯合股份公司 共濟失調毛細血管擴張症和Rad3相關激酶抑制劑
WO2025240847A1 (en) 2024-05-17 2025-11-20 Revolution Medicines, Inc. Ras inhibitors
US20250375445A1 (en) 2024-06-07 2025-12-11 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
WO2025265060A1 (en) 2024-06-21 2025-12-26 Revolution Medicines, Inc. Therapeutic compositions and methods for managing treatment-related effects
WO2026006747A1 (en) 2024-06-28 2026-01-02 Revolution Medicines, Inc. Ras inhibitors
WO2026015825A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Use of ras inhibitor for treating pancreatic cancer
WO2026015796A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015790A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015801A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026050446A1 (en) 2024-08-29 2026-03-05 Revolution Medicines, Inc. Ras inhibitors
WO2026072904A2 (en) 2024-09-26 2026-04-02 Revolution Medicines, Inc. Compositions and methods for treating lung cancer

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EP3795573B1 (en) * 2009-12-31 2022-07-06 Hutchison Medipharma Limited Certain triazolopyrazines, compositions thereof and methods of use therefor
JP5889875B2 (ja) * 2010-05-07 2016-03-22 グラクソスミスクライン・リミテッド・ライアビリティ・カンパニーGlaxoSmithKline LLC アザインダゾール
ES2951688T3 (es) * 2011-02-28 2023-10-24 Epizyme Inc Compuestos de heteroarilo biciclico fusionados en 6,5 sustituidos
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WO2013067302A1 (en) * 2011-11-04 2013-05-10 Glaxosmithkline Intellectual Property (No. 2) Limited Method of treatment
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TWI700283B (zh) * 2014-08-04 2020-08-01 德商拜耳製藥公司 2-(嗎啉-4-基)-1,7-萘啶
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CR20210281A (es) * 2018-10-30 2021-10-25 Repare Therapeutics Inc Compuestos, composiciones farmacéuticas y métodos de preparación de compuestos y de uso como inhibidores de la cinasa atr
MX2022000854A (es) * 2019-07-22 2022-02-10 Repare Therapeutics Inc Derivados de 2-morfolinopiridina sustituidos como inhibidores de la cinasa atr.

Also Published As

Publication number Publication date
JP2022541825A (ja) 2022-09-27
JP2025061048A (ja) 2025-04-10
MX2022000854A (es) 2022-02-10
ECSP22012347A (es) 2022-03-31
CA3148278A1 (en) 2021-01-28
KR20220035925A (ko) 2022-03-22
AU2020317381A1 (en) 2022-02-10
BR112022000431A2 (pt) 2022-03-03
UA129807C2 (uk) 2025-08-06
WO2021012049A8 (en) 2021-04-15
EP4003993A4 (en) 2023-01-18
EP4003993A1 (en) 2022-06-01
CN114174292B (zh) 2024-06-18
PH12022550156A1 (en) 2023-05-08
WO2021012049A1 (en) 2021-01-28
CO2022001853A2 (es) 2022-03-29
US20220185809A1 (en) 2022-06-16
JP7617076B2 (ja) 2025-01-17
IL289763A (en) 2022-03-01
CN114174292A (zh) 2022-03-11
JP7758895B2 (ja) 2025-10-22

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