JP2023550591A5 - - Google Patents

Info

Publication number
JP2023550591A5
JP2023550591A5 JP2023526609A JP2023526609A JP2023550591A5 JP 2023550591 A5 JP2023550591 A5 JP 2023550591A5 JP 2023526609 A JP2023526609 A JP 2023526609A JP 2023526609 A JP2023526609 A JP 2023526609A JP 2023550591 A5 JP2023550591 A5 JP 2023550591A5
Authority
JP
Japan
Prior art keywords
alkyl
group
membered
cycloalkyl
haloalkyl
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.)
Granted
Application number
JP2023526609A
Other languages
English (en)
Japanese (ja)
Other versions
JP2023550591A (ja
JP7805363B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2021/080151 external-priority patent/WO2022090481A1/en
Publication of JP2023550591A publication Critical patent/JP2023550591A/ja
Publication of JP2023550591A5 publication Critical patent/JP2023550591A5/ja
Application granted granted Critical
Publication of JP7805363B2 publication Critical patent/JP7805363B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2023526609A 2020-11-02 2021-10-29 EGFR阻害薬としての置換1H-ピラゾロ[4,3-c]及び誘導体 Active JP7805363B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP20205297.3 2020-11-02
EP20205297 2020-11-02
PCT/EP2021/080151 WO2022090481A1 (en) 2020-11-02 2021-10-29 Substituted 1h-pyrazolo[4,3-c]pyridines and derivatives as egfr inhibitors

Publications (3)

Publication Number Publication Date
JP2023550591A JP2023550591A (ja) 2023-12-04
JP2023550591A5 true JP2023550591A5 (enExample) 2024-11-05
JP7805363B2 JP7805363B2 (ja) 2026-01-23

Family

ID=73059474

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2023526609A Active JP7805363B2 (ja) 2020-11-02 2021-10-29 EGFR阻害薬としての置換1H-ピラゾロ[4,3-c]及び誘導体

Country Status (7)

Country Link
US (2) US12064421B2 (enExample)
EP (1) EP4237423B1 (enExample)
JP (1) JP7805363B2 (enExample)
CN (1) CN116507627B (enExample)
AR (1) AR123977A1 (enExample)
TW (1) TW202233637A (enExample)
WO (1) WO2022090481A1 (enExample)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW202309022A (zh) 2021-04-13 2023-03-01 美商努法倫特公司 用於治療具egfr突變之癌症之胺基取代雜環
WO2024181803A1 (ko) * 2023-02-28 2024-09-06 보로노이 주식회사 헤테로아릴 유도체 및 이의 용도
KR20240152239A (ko) * 2023-04-11 2024-10-21 보로노이 주식회사 피라졸로피리딘 유도체 화합물 및 이의 용도
CN117069746B (zh) * 2023-08-17 2025-10-21 苏州共康医药科技有限公司 取代的吡唑并吡啶类化合物作为4代egfr抑制剂

Family Cites Families (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2003220970A1 (en) 2002-03-01 2003-09-16 Smithkline Beecham Corporation Diamino-pyrimidines and their use as angiogenesis inhibitors
US20050154202A1 (en) 2002-04-05 2005-07-14 Hagmann William K. Substituted aryl amides
NZ543482A (en) 2003-05-21 2009-02-28 Prosidion Ltd Pyrrolopyridine-2-carboxylic acid amide inhibitors of glycogen phoshorylase
US7557211B2 (en) 2004-11-12 2009-07-07 Bristol-Myers Squibb Company 8H-imidazo[4,5-D]thiazolo[4,5-B]pyridine based tricyclic compounds and pharmaceutical compositions comprising same
US7737279B2 (en) 2005-05-10 2010-06-15 Bristol-Myers Squibb Company 1,6-dihydro-1,3,5,6-tetraaza-as-indacene based tricyclic compounds and pharmaceutical compositions comprising same
TW200803855A (en) 2006-02-24 2008-01-16 Kalypsys Inc Quinolones useful as inducible nitric oxide synthase inhibitors
EP2114916A2 (en) 2007-02-02 2009-11-11 NeuroSearch A/S Pyridinyl-pyrazole derivatives and their use as potassium channel modulators
US8865732B2 (en) 2008-03-21 2014-10-21 Novartis Ag Heterocyclic compounds and uses thereof
TWI501967B (zh) 2010-12-16 2015-10-01 Janssen R&D Ireland 作為呼吸道融合病毒抗病毒劑之氮雜吲哚類
US9527925B2 (en) 2011-04-01 2016-12-27 Boehringer Ingelheim International Gmbh Bispecific binding molecules binding to VEGF and ANG2
WO2013056679A1 (en) 2011-10-21 2013-04-25 Beijing Hanmi Pharmaceutical Co., Ltd Novel heteroaryl-amino derivatives
AR090151A1 (es) 2012-03-07 2014-10-22 Lilly Co Eli Compuestos inhibidores de raf
JO3300B1 (ar) 2012-06-06 2018-09-16 Novartis Ag مركبات وتركيبات لتعديل نشاط egfr
US20150152083A1 (en) 2012-06-06 2015-06-04 Irm Llc, A Delaware Limited Liability Company Compounds and Compositions for Modulating EGFR Activity
MX2014014828A (es) * 2012-06-27 2015-02-12 Hoffmann La Roche Compuestos de 5-azaindazol y metodos de uso.
RU2660429C2 (ru) 2012-09-28 2018-07-06 Мерк Шарп И Доум Корп. Новые соединения, которые являются ингибиторами erk
WO2014081718A1 (en) 2012-11-20 2014-05-30 Genentech, Inc. Aminopyrimidine compounds as inhibitors of t790m containing egfr mutants
US9242969B2 (en) 2013-03-14 2016-01-26 Novartis Ag Biaryl amide compounds as kinase inhibitors
WO2014210354A1 (en) 2013-06-28 2014-12-31 Genentech, Inc. Azaindazole compounds as inhibitors of t790m containing egfr mutants
CN105658639A (zh) 2013-08-22 2016-06-08 豪夫迈·罗氏有限公司 炔基醇和应用方法
CN104418858B (zh) 2013-08-30 2018-12-11 浙江医药股份有限公司新昌制药厂 2,6-二含氮取代的嘌呤衍生物及其制备方法和其药物组合物与应用
WO2015094929A1 (en) 2013-12-18 2015-06-25 Merck Sharp & Dohme Corp. Erk inhibitors
LT3466955T (lt) 2014-01-13 2021-02-25 Aurigene Discovery Technologies Limited Oksazol[4,5-b]piridino ir tiazol[4,5-b]piridino darinių, kaip irak4 inhibitorių, skirtų vėžio gydymui, gamybos būdas
JP6568926B2 (ja) 2014-03-20 2019-08-28 カペラ セラピューティクス,インコーポレーテッド 癌の治療のためのerbbチロシンキナーゼ阻害剤としてのベンゾイミダゾール誘導体
CA2943220C (en) 2014-03-20 2024-01-16 Capella Therapeutics, Inc. Benzimidazole derivatives as erbb tyrosine kinase inhibitors for the treatment of cancer
CN105315285B (zh) * 2014-07-25 2017-12-08 上海海雁医药科技有限公司 2,4‑二取代7H‑吡咯并[2,3‑d]嘧啶衍生物、其制法与医药上的用途
EP3270694A4 (en) * 2015-02-17 2018-09-05 Neupharma, Inc. Certain chemical entities, compositions, and methods
CN108012529A (zh) 2015-05-15 2018-05-08 诺华股份有限公司 治疗egfr突变的癌症的方法
UA124090C2 (uk) 2015-06-03 2021-07-21 Прінсіпіа Байофарма Інк. Інгібітори тирозинкінази
JP6845165B2 (ja) 2015-06-30 2021-03-17 デイナ ファーバー キャンサー インスティチュート,インコーポレイテッド Egfr阻害剤およびその使用方法
EP3347353B1 (en) 2015-09-11 2019-07-17 Boehringer Ingelheim International GmbH Pyrazolyl-substituted heteroaryls and their use as medicaments
TWI726968B (zh) 2016-01-07 2021-05-11 開曼群島商Cs醫藥技術公司 Egfr酪胺酸激酶之臨床重要突變體之選擇性抑制劑
EP3535258B1 (en) 2016-11-03 2021-11-24 Bristol-Myers Squibb Company Substituted bicycle heterocyclic derivatives useful as romk channel inhibitors
US11198726B2 (en) 2017-06-02 2021-12-14 Boerhinger Ingelheim International Gmbh Anti-cancer combination therapy
EP3717471B1 (en) 2017-12-02 2022-01-05 Galapagos NV Novel compounds and pharmaceutical compositions thereof for the treatment of diseases
JP7313364B2 (ja) * 2018-02-21 2023-07-24 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング Egfr阻害剤としての新たなベンズイミダゾール化合物および誘導体
WO2020178316A1 (en) * 2019-03-05 2020-09-10 Aziende Chimiche Riunite Angelini Francesco - A.C.R.A.F. S.P.A. 5- or 7-azaindazoles as beta-lactamase inhibitors

Similar Documents

Publication Publication Date Title
JP2023550591A5 (enExample)
JP2014500295A5 (enExample)
JOP20220271A1 (ar) مركبات دايازينو بيريميدين كمثبطات لـ her2
JP2019517487A5 (enExample)
JP2016501189A5 (enExample)
JP2012532136A5 (enExample)
RU2650895C2 (ru) Соединения замещенных пиразолонов и способы использования
EP3277276B1 (en) Methods of administering glutaminase inhibitors
JP2022545359A5 (enExample)
JP2013502431A5 (enExample)
JP2017511360A5 (enExample)
RU2015118647A (ru) Аминопиримидиновые соединения в качестве ингибиторов содержащих т790м мутантных egfr
JP2005533748A5 (enExample)
JP2014503567A5 (enExample)
JP2017528498A5 (enExample)
JP2017519781A5 (enExample)
AU2025204720A1 (en) Methods for treating testicular and ovarian adrenal rest tumors
RU2014115847A (ru) Пирролопиримидиновые соединения для лечения злокачественной опухоли
JP2020527173A5 (enExample)
JP2014512364A5 (enExample)
HRP20220351T1 (hr) 3,5-disupstituirani pirazoli korisni kao inhibitori kinaze 1 kontrolne točke (chk1), i njihove pripreme i primjene
BR112013021941B1 (pt) Agente terapêutico para tumor
AR079029A1 (es) Derivados de pirimidil-amino-benzamida para tratar trastornos proliferativos y otras condiciones patologicas mediadas por la actividad de cinasa de bcr-abl, c-kit, ddr1, ddr2 o pdgf-r
SI3166925T1 (en) Isoindoline derivatives for use in treating a viral infection
JP2013542267A5 (enExample)