MX2022000854A - 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
MX2022000854A
MX2022000854A MX2022000854A MX2022000854A MX2022000854A MX 2022000854 A MX2022000854 A MX 2022000854A MX 2022000854 A MX2022000854 A MX 2022000854A MX 2022000854 A MX2022000854 A MX 2022000854A MX 2022000854 A MX2022000854 A MX 2022000854A
Authority
MX
Mexico
Prior art keywords
optionally substituted
alkyl
substituted
morpholinopyridine
derivatives
Prior art date
Application number
MX2022000854A
Other languages
English (en)
Inventor
Lee Fader
Sheldon N Crane
Vouy Linh Truong
Abbas Abdoli
Jean- François TRUCHON
Cameron Black
Stéphane Dorich
Paul Jones
Miguel St-Onge
Audrey Picard
Cyrus M Lacbay
Stéphane LANOIX
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 MX2022000854A publication Critical patent/MX2022000854A/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic 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
    • C07D471/02—Heterocyclic 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
    • C07D471/04—Ortho-condensed systems
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535—Heterocyclic 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
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents

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.
MX2022000854A 2019-07-22 2020-07-22 Derivados de 2-morfolinopiridina sustituidos como inhibidores de la cinasa atr. MX2022000854A (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
MX2022000854A true MX2022000854A (es) 2022-02-10

Family

ID=74192632

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2022000854A MX2022000854A (es) 2019-07-22 2020-07-22 Derivados de 2-morfolinopiridina sustituidos como inhibidores de la cinasa atr.

Country Status (14)

Country Link
US (1) US20220185809A1 (es)
EP (1) EP4003993A4 (es)
JP (1) JP2022541825A (es)
KR (1) KR20220035925A (es)
CN (1) CN114174292A (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)
WO (1) WO2021012049A1 (es)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4072551A4 (en) * 2019-12-11 2023-11-15 Repare Therapeutics Inc. USE OF ATR INHIBITORS IN COMBINATION WITH PARP INHIBITORS
WO2022226655A1 (en) * 2021-04-28 2022-11-03 Repare Therapeutics Inc. Methods of treating cancers having a biallelic loss of function or gene overexpression mutation
AU2022284632A1 (en) * 2021-06-04 2023-12-07 Repare Therapeutics Inc. Crystalline forms, compositions containing same, and methods of their use
TW202321256A (zh) * 2021-07-27 2023-06-01 大陸商上海輝啟生物醫藥科技有限公司 ８－氧－３－氮雜雙環［３．２．１］辛烷類化合物或其鹽及其製備方法和用途
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
CN116099390A (zh) * 2022-11-14 2023-05-12 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

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106432225B (zh) * 2009-12-31 2019-02-19 和记黄埔医药（上海）有限公司 某些三唑并吡啶化合物和三唑并吡嗪化合物、其组合物和其使用方法
EP2566479B1 (en) * 2010-05-07 2014-12-24 GlaxoSmithKline LLC Azaindazoles
EP2681216B1 (en) * 2011-02-28 2017-09-27 Epizyme, Inc. Substituted 6,5-fused bicyclic heteroaryl compounds
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
US8906910B2 (en) * 2011-12-20 2014-12-09 Glaxosmithkline Llc Imidazopyridine derivatives as PI3 kinase
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
CN107835814B (zh) * 2015-04-29 2021-07-23 詹森药业有限公司 氮杂苯并咪唑及其作为ampa受体调节剂的用途
EP3402795B1 (en) * 2016-01-14 2019-10-30 Bayer Pharma Aktiengesellschaft 5-substituted 2-(morpholin-4-yl)-1,7-naphthyridines
WO2020087170A1 (en) * 2018-10-30 2020-05-07 Repare Therapeutics Inc. Compounds, pharmaceutical compositions, and methods of preparing compounds and of their use as atr kinase inhibitors

Also Published As

Publication number Publication date
IL289763A (en) 2022-03-01
CO2022001853A2 (es) 2022-03-29
CN114174292A (zh) 2022-03-11
ECSP22012347A (es) 2022-03-31
EP4003993A1 (en) 2022-06-01
AU2020317381A1 (en) 2022-02-10
EP4003993A4 (en) 2023-01-18
CR20220068A (es) 2022-06-30
BR112022000431A2 (pt) 2022-03-03
CA3148278A1 (en) 2021-01-28
US20220185809A1 (en) 2022-06-16
KR20220035925A (ko) 2022-03-22
WO2021012049A1 (en) 2021-01-28
JP2022541825A (ja) 2022-09-27
WO2021012049A8 (en) 2021-04-15

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