CO2022001853A2 - 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
CO2022001853A2
CO2022001853A2 CONC2022/0001853A CO2022001853A CO2022001853A2 CO 2022001853 A2 CO2022001853 A2 CO 2022001853A2 CO 2022001853 A CO2022001853 A CO 2022001853A CO 2022001853 A2 CO2022001853 A2 CO 2022001853A2
Authority
CO
Colombia
Prior art keywords
optionally substituted
alkyl
inhibitors
substituted
morpholinopyridine
Prior art date
Application number
CONC2022/0001853A
Other languages
English (en)
Spanish (es)
Inventor
Sheldon N Crane
Vouy Linh Truong
Abbas Abdoli
Jean-François Truchon
Cameron Black
Stéphane Dorich
Lee Fader
Stéphanie Lanoix
Paul Jones
Miguel St-Onge
Audrey Picard
Cyrus M Lacbay
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 CO2022001853A2 publication Critical patent/CO2022001853A2/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)
CONC2022/0001853A 2019-07-22 2022-02-22 Derivados de 2-morfolinopiridina sustituidos como inhibidores de la cinasa atr CO2022001853A2 (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
CO2022001853A2 true CO2022001853A2 (es) 2022-03-29

Family

ID=74192632

Family Applications (1)

Application Number Title Priority Date Filing Date
CONC2022/0001853A CO2022001853A2 (es) 2019-07-22 2022-02-22 Derivados de 2-morfolinopiridina sustituidos como inhibidores de la cinasa atr

Country Status (16)

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

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
EP2755962B1 (en) * 2011-09-13 2017-03-01 Glaxosmithkline LLC Azaindazoles
WO2013067302A1 (en) * 2011-11-04 2013-05-10 Glaxosmithkline Intellectual Property (No. 2) Limited Method of treatment
WO2013095761A1 (en) * 2011-12-20 2013-06-27 Glaxosmithkline Llc Imidazopyridine derivatives as pi3 kinase inhibitors
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
RS61688B1 (sr) * 2015-04-29 2021-05-31 Janssen Pharmaceutica Nv Azabenzimidazoli i njihiova upotreba kao modulatori ampa receptora
JP6873145B2 (ja) * 2016-01-14 2021-05-19 バイエル・ファルマ・アクティエンゲゼルシャフト 5−置換2−(モルホリン−4−イル)−1,7−ナフチリジン
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
CR20220068A (es) 2022-06-30
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
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

Similar Documents

Publication Publication Date Title
CO2022001853A2 (es) Derivados de 2-morfolinopiridina sustituidos como inhibidores de la cinasa atr
AR130689A1 (es) Inhibidores heterocíclicos anclados de proteínas kras g12c mutantes y usos de estos
PE20230825A1 (es) Inhibidores de kras triciclicos fusionados
PE20220931A1 (es) Inhibidores de shp2 fosfatasa de tipo pirazolo[3,4-b]pirazina
MX2019011693A (es) Compuestos que inhiben la proteina mcl-1.
UY26968A1 (es) Agentes terapéuticos
CL2012001699A1 (es) Compuestos derivados de n-(1h-indazol-4-il)imidazo[1,2-a]piridin-3-carboxamida sustituidos, inhibidores de cfms; proceso de preparacion; composicion farmaceutica que los comprende; uso del compuesto para el tratamiento de enfermedades relacionadas con huesos, cancer, trastornos autoinmunes, enfermedades inflamatorias, entre otras.
PE20191613A1 (es) Compuestos de pirazolo[1,5-a]piridina sustituidos como inhibidores de la quinasa ret
ECSP056194A (es) Derivados de pirazolo-quinazolina, procedimiento para su preparacion y su uso como inhibidores de quinasa
CO2017004481A2 (es) Compuestos de indol carboxamida utiles como inhibidores de cinasas
EA201891191A1 (ru) 2-замещенные соединения хиназолина, содержащие замещенную гетероциклическую группу, и способы их применения
EA201070167A1 (ru) Замещенные производные индазола, активные как ингибиторы киназы
AR024060A1 (es) Nuevos compuestos farmaceuticamente activos
AR016762A1 (es) Compuestos del acido 4-bromo o 4-yodo fenilamino benzohidroxamico, formulaciones farmaceuticas y uso del mismo
ECSP088973A (es) Derivados de imidazol pirimidina para el tratamiento de enfermedades relacionadas con la glicógeno sintasa quinasa (gsk3)
EA200970611A1 (ru) Замещенные пиразолохиназолиновые производные, способ их получения и их применение в качестве ингибиторов киназы
AR040580A1 (es) Derivados de pirazol heterobiciclico como inhibidores de la quinasa
MX2024013019A (es) Compuestos de heteroarilo para el tratamiento del dolor
CO2020004669A2 (es) Derivados de bencimidazol y sus usos
MX389581B (es) Compuestos que contienen nitrogeno sustituido.
EA201990765A1 (ru) Азаиндазольные соединения для применения при повреждениях сухожилий и/или связок
UY38233A (es) Agentes inhibidores para la tirosina cinasa de bruton
MX2021012248A (es) Polimorfos de voruciclib y metodos de elaboracion y uso de los mismos.
MX2018013325A (es) Derivados de adenina como inhibidores de proteína quinasa.
DOP2020000088A (es) Derivados de piridinona y su uso como inhibidores selectivos de alk–2.