HK1202541A1 - 2-amino, 6-phenyl substituted pyrido [2, 3 - d] pyrimidine derivatives useful as raf kinase inhibitors raf 2-, 6-[2,3-d] - Google Patents

2-amino, 6-phenyl substituted pyrido [2, 3 - d] pyrimidine derivatives useful as raf kinase inhibitors raf 2-, 6-[2,3-d]

Info

Publication number
HK1202541A1
HK1202541A1 HK15103082.6A HK15103082A HK1202541A1 HK 1202541 A1 HK1202541 A1 HK 1202541A1 HK 15103082 A HK15103082 A HK 15103082A HK 1202541 A1 HK1202541 A1 HK 1202541A1
Authority
HK
Hong Kong
Prior art keywords
raf
amino
kinase inhibitors
phenyl substituted
pyrimidine derivatives
Prior art date
Application number
HK15103082.6A
Other languages
English (en)
Chinese (zh)
Inventor
Matthew Carl Allgeier
Daniel L Flynn
Michael D Kaufman
Phenil J Patel
Craig D Wolfangel
Original Assignee
Lilly Co Eli
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=47884613&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=HK1202541(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Lilly Co Eli filed Critical Lilly Co Eli
Publication of HK1202541A1 publication Critical patent/HK1202541A1/xx

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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4985Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • 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
    • C07D471/12Heterocyclic 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 three hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicinal Preparation (AREA)
HK15103082.6A 2012-03-07 2015-03-26 2-amino, 6-phenyl substituted pyrido [2, 3 - d] pyrimidine derivatives useful as raf kinase inhibitors raf 2-, 6-[2,3-d] HK1202541A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201261607702P 2012-03-07 2012-03-07
PCT/US2013/029084 WO2013134243A1 (fr) 2012-03-07 2013-03-05 Dérivés de 2-amino, 6-phenyl à substitution pyrido [2, 3 - d] pyrimidine utilisés en tant qu'inhibiteurs de la raf kinase

Publications (1)

Publication Number Publication Date
HK1202541A1 true HK1202541A1 (en) 2015-10-02

Family

ID=47884613

Family Applications (1)

Application Number Title Priority Date Filing Date
HK15103082.6A HK1202541A1 (en) 2012-03-07 2015-03-26 2-amino, 6-phenyl substituted pyrido [2, 3 - d] pyrimidine derivatives useful as raf kinase inhibitors raf 2-, 6-[2,3-d]

Country Status (39)

Country Link
US (2) US8741911B2 (fr)
EP (1) EP2850082B1 (fr)
JP (1) JP2015509536A (fr)
KR (1) KR20140129087A (fr)
CN (1) CN104302646B (fr)
AP (1) AP2014007899A0 (fr)
AR (1) AR090151A1 (fr)
AU (1) AU2013230146B2 (fr)
BR (1) BR112014018528A8 (fr)
CA (1) CA2863673A1 (fr)
CL (1) CL2014002220A1 (fr)
CO (1) CO7010837A2 (fr)
CR (1) CR20140378A (fr)
CY (1) CY1117846T1 (fr)
DK (1) DK2850082T3 (fr)
DO (1) DOP2014000200A (fr)
EA (1) EA024824B1 (fr)
EC (1) ECSP14017584A (fr)
ES (1) ES2584387T3 (fr)
HK (1) HK1202541A1 (fr)
HR (1) HRP20160654T1 (fr)
HU (1) HUE028095T2 (fr)
IL (1) IL234052A (fr)
IN (1) IN2014MN01575A (fr)
LT (1) LT2850082T (fr)
MA (1) MA37316B1 (fr)
ME (1) ME02423B (fr)
MX (1) MX2014010701A (fr)
NZ (1) NZ627454A (fr)
PE (1) PE20142338A1 (fr)
PH (1) PH12014501986A1 (fr)
PT (1) PT2850082T (fr)
RS (1) RS54840B1 (fr)
SG (1) SG11201404969YA (fr)
SI (1) SI2850082T1 (fr)
TN (1) TN2014000375A1 (fr)
TW (1) TW201348233A (fr)
UA (1) UA112340C2 (fr)
WO (2) WO2013134252A1 (fr)

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TWI704151B (zh) 2014-12-22 2020-09-11 美商美國禮來大藥廠 Erk抑制劑
MX2018015353A (es) * 2016-06-10 2019-09-09 Novartis Ag Usos terapeuticos de un inhibidor de c-raf.
EP3878850A1 (fr) 2016-12-22 2021-09-15 Boehringer Ingelheim International GmbH Nouvelles quinazolines substituées benzylamino et dérivés en tant qu'inhibiteurs de sos1
CA3060147A1 (fr) * 2017-04-28 2018-11-01 Quartz Therapeutics, Inc. Composes conjugues de degradation de raf
JOP20200154A1 (ar) 2017-12-21 2020-06-18 Boehringer Ingelheim Int مركبات ومشتقات بيريدو بيريمينون بها استبدال ببنزيل أمينو جديدة كمثبطات sos1
JP7161849B2 (ja) * 2018-01-24 2022-10-27 株式会社クラレ 第一級アミンの製造方法
CN111818915B (zh) 2018-01-31 2024-05-24 德西费拉制药有限责任公司 治疗胃肠道间质瘤的组合疗法
EP3849536A4 (fr) 2018-09-10 2022-06-29 Mirati Therapeutics, Inc. Polythérapies
AU2019416117B2 (en) 2018-12-28 2024-05-02 Deciphera Pharmaceuticals, Llc CSF1R inhibitors for use in treating cancer
WO2020163268A1 (fr) 2019-02-06 2020-08-13 Eli Lilly And Company Dérivés de 1-((2-(2,2,2-trifluoroéthoxy)pyridin-4-yl) méthyl)urée en tant que potentialisateurs de kcnq
CA3138300A1 (fr) * 2019-05-03 2020-11-12 Kinnate Biopharma Inc. Inhibiteurs de kinases raf
PL3966207T3 (pl) 2019-05-10 2024-03-04 Deciphera Pharmaceuticals, Llc Fenyloaminopirymidynoamidowe inhibitory autofagii i sposoby ich zastosowania
CN114072397A (zh) 2019-05-10 2022-02-18 德西费拉制药有限责任公司 杂芳基氨基嘧啶酰胺自噬抑制剂及其使用方法
AU2020297422B2 (en) 2019-06-17 2024-03-21 Deciphera Pharmaceuticals, Llc Aminopyrimidine amide autophagy inhibitors and methods of use thereof
WO2021030405A1 (fr) 2019-08-12 2021-02-18 Deciphera Pharmaceuticals, Llc Ripretinib pour le traitement de tumeurs stromales gastro-intestinales
EP4013412A1 (fr) 2019-08-12 2022-06-22 Deciphera Pharmaceuticals, LLC Ripretinib pour le traitement de tumeurs stromales gastro-intestinales
KR20220123057A (ko) 2019-12-30 2022-09-05 데시페라 파마슈티칼스, 엘엘씨. 비정질 키나아제 억제제 제형 및 이의 사용 방법
EP4084779A1 (fr) 2019-12-30 2022-11-09 Deciphera Pharmaceuticals, LLC Compositions de 1-(4-bromo-5-(1-éthyl-7-(méthylamino)-2-oxo-1,2-dihydro -1,6-naphthyridine-3-yl)-2-fluorophényl)-3-phényluree
BR112022023462A2 (pt) 2020-06-02 2022-12-20 Boehringer Ingelheim Int 2-amino-3-ciano tiofenos anulados e derivados para o tratamento de câncer
US11407737B2 (en) 2020-09-18 2022-08-09 Kinnate Biopharma Inc. Inhibitors of RAF kinases
US11377431B2 (en) 2020-10-12 2022-07-05 Kinnate Biopharma Inc. Inhibitors of RAF kinases
EP4237423A1 (fr) 2020-11-02 2023-09-06 Boehringer Ingelheim International GmbH 1h-pyrazolo[4,3-c]pyridines substituées et leurs dérivés utilisés comme inhibiteurs d'egfr
WO2022109001A1 (fr) 2020-11-18 2022-05-27 Deciphera Pharmaceuticals, Llc Inhibiteurs des kinases gcn2 et perk et leurs méthodes d'utilisation
EP4267250A1 (fr) 2020-12-22 2023-11-01 Qilu Regor Therapeutics Inc. Inhibiteurs de sos1 et utilisations associées
WO2022226261A1 (fr) 2021-04-23 2022-10-27 Kinnate Biopharma Inc. Traitement du cancer avec un inhibiteur de raf
US20220388986A1 (en) 2021-04-29 2022-12-08 Boehringer Ingelheim International Gmbh Heterocyclic compounds capable of activating sting
TW202340209A (zh) 2021-12-01 2023-10-16 德商百靈佳殷格翰國際股份有限公司 用於治療癌症之環狀2-胺基-3-氰基噻吩及衍生物
TW202337432A (zh) 2021-12-01 2023-10-01 德商百靈佳殷格翰國際股份有限公司 用於治療癌症之環狀2-胺基-3-氰基噻吩及衍生物
WO2023099620A1 (fr) 2021-12-01 2023-06-08 Boehringer Ingelheim International Gmbh Composés de dégradation de kras comprenant des 2-amino-3-cyano thiophènes annelés
WO2023099592A1 (fr) 2021-12-01 2023-06-08 Boehringer Ingelheim International Gmbh 2-amino-3-cyano thiophènes annelés et leurs dérivés pour le traitement du cancer
WO2023099623A1 (fr) 2021-12-01 2023-06-08 Boehringer Ingelheim International Gmbh 2-amino-3-cyano-thiophènes annelés et dérivés pour le traitement du cancer
AU2022402390A1 (en) 2021-12-01 2024-05-30 Boehringer Ingelheim International Gmbh Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
CA3240192A1 (fr) 2021-12-09 2023-06-15 Daniel L. Flynn Inhibiteurs de kinase raf et leurs procedes d'utilisation
WO2023118250A1 (fr) 2021-12-23 2023-06-29 Boehringer Ingelheim International Gmbh 8-aza-quinazolines utilisés en tant qu'inhibiteurs de sos1 pénétrant dans le cerveau
WO2023173017A1 (fr) * 2022-03-09 2023-09-14 Blossomhill Therapeutics, Inc. Inhibiteurs de kras pour le traitement d'une maladie
US11779572B1 (en) 2022-09-02 2023-10-10 Deciphera Pharmaceuticals, Llc Methods of treating gastrointestinal stromal tumors
US20240166629A1 (en) 2022-10-26 2024-05-23 Boehringer Ingelheim International Gmbh Heterocyclic compounds capable of activating sting
WO2024089006A1 (fr) 2022-10-26 2024-05-02 Boehringer Ingelheim International Gmbh Composés hétérocycliques capables d'activer sting
US20240174642A1 (en) 2022-10-26 2024-05-30 Boehringer Ingelheim International Gmbh Heterocyclic compounds capable of activating sting

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WO2003033472A1 (fr) * 2001-10-17 2003-04-24 Kirin Beer Kabushiki Kaisha Derives de quinoline ou de quinazoline inhibant l'autophosphorylation de recepteurs du facteur de croissance des fibroblastes
EP1566379A4 (fr) * 2002-10-29 2005-11-09 Kirin Brewery DERIVES DE QUINOLINE ET DE QUINAZOLINE INHIBANT L'AUTOPHOSPHORYLATION DE Flt3 ET COMPOSITIONS MEDICALES LES CONTENANT
US20070054916A1 (en) 2004-10-01 2007-03-08 Amgen Inc. Aryl nitrogen-containing bicyclic compounds and methods of use
US7897762B2 (en) 2006-09-14 2011-03-01 Deciphera Pharmaceuticals, Llc Kinase inhibitors useful for the treatment of proliferative diseases
US8188113B2 (en) * 2006-09-14 2012-05-29 Deciphera Pharmaceuticals, Inc. Dihydropyridopyrimidinyl, dihydronaphthyidinyl and related compounds useful as kinase inhibitors for the treatment of proliferative diseases
AR080151A1 (es) * 2010-02-09 2012-03-14 Exelixis Inc Metodos para tratar cancer usando inhibidores de piridopirimidinona de pi 3k y mtor en combinacion con inhibidores de autofagia
AR090151A1 (es) * 2012-03-07 2014-10-22 Lilly Co Eli Compuestos inhibidores de raf

Also Published As

Publication number Publication date
KR20140129087A (ko) 2014-11-06
BR112014018528A8 (pt) 2017-07-11
EP2850082A1 (fr) 2015-03-25
CN104302646A (zh) 2015-01-21
EP2850082B1 (fr) 2016-05-18
DOP2014000200A (es) 2014-10-15
MA37316A1 (fr) 2016-06-30
DK2850082T3 (en) 2016-08-15
PH12014501986B1 (en) 2014-11-24
CA2863673A1 (fr) 2013-09-12
EA024824B1 (ru) 2016-10-31
CN104302646B (zh) 2016-05-04
HRP20160654T1 (hr) 2016-07-01
PE20142338A1 (es) 2015-01-10
TW201348233A (zh) 2013-12-01
AU2013230146B2 (en) 2015-09-10
CR20140378A (es) 2014-11-27
AR090151A1 (es) 2014-10-22
WO2013134243A1 (fr) 2013-09-12
LT2850082T (lt) 2016-09-12
SG11201404969YA (en) 2014-10-30
AP2014007899A0 (en) 2014-08-31
CY1117846T1 (el) 2017-05-17
NZ627454A (en) 2016-09-30
CL2014002220A1 (es) 2015-06-05
ECSP14017584A (es) 2016-01-29
RS54840B1 (sr) 2016-10-31
MA37316B1 (fr) 2017-03-31
UA112340C2 (uk) 2016-08-25
US20150119392A1 (en) 2015-04-30
MX2014010701A (es) 2015-03-10
PT2850082T (pt) 2016-07-15
ME02423B (fr) 2016-09-20
US9334267B2 (en) 2016-05-10
PH12014501986A1 (en) 2014-11-24
CO7010837A2 (es) 2014-07-31
BR112014018528A2 (fr) 2017-06-20
EA201491456A1 (ru) 2014-12-30
SI2850082T1 (sl) 2016-07-29
US8741911B2 (en) 2014-06-03
US20130252977A1 (en) 2013-09-26
TN2014000375A1 (en) 2015-12-21
ES2584387T3 (es) 2016-09-27
AU2013230146A1 (en) 2014-08-14
IN2014MN01575A (fr) 2015-05-08
IL234052A (en) 2016-05-31
JP2015509536A (ja) 2015-03-30
WO2013134252A1 (fr) 2013-09-12
HUE028095T2 (en) 2016-11-28

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