SG11201700957WA - Aminopyrimidinyl compounds as jak inhibitors - Google Patents

Aminopyrimidinyl compounds as jak inhibitors

Info

Publication number
SG11201700957WA
SG11201700957WA SG11201700957WA SG11201700957WA SG11201700957WA SG 11201700957W A SG11201700957W A SG 11201700957WA SG 11201700957W A SG11201700957W A SG 11201700957WA SG 11201700957W A SG11201700957W A SG 11201700957WA SG 11201700957W A SG11201700957W A SG 11201700957WA
Authority
SG
Singapore
Prior art keywords
jak inhibitors
aminopyrimidinyl
compounds
aminopyrimidinyl compounds
jak
Prior art date
Application number
SG11201700957WA
Inventor
Andrew Fensome
Ariamala Gopalsamy
Brian S Gerstenberger
Ivan Viktorovich Efremov
Zhao-Kui Wan
Betsy PIERCE
Jean-Baptiste Telliez
John I Trujillo
Liying Zhang
Li Xing
Eddine Saiah
Original Assignee
Pfizer
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=54148580&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SG11201700957W(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Pfizer filed Critical Pfizer
Publication of SG11201700957WA publication Critical patent/SG11201700957WA/en

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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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    • 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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    • HELECTRICITY
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SG11201700957WA 2014-08-21 2015-08-07 Aminopyrimidinyl compounds as jak inhibitors SG11201700957WA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201462039969P 2014-08-21 2014-08-21
PCT/IB2015/056021 WO2016027195A1 (en) 2014-08-21 2015-08-07 Aminopyrimidinyl compounds as jak inhibitors

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SG11201700957WA true SG11201700957WA (en) 2017-03-30

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EP (1) EP3183247B9 (en)
JP (1) JP6218260B2 (en)
KR (1) KR101877189B1 (en)
CN (1) CN107074867B (en)
AP (1) AP2017009748A0 (en)
AR (1) AR101599A1 (en)
AU (1) AU2015304883B2 (en)
BR (1) BR112017003054B1 (en)
CA (1) CA2900855C (en)
CL (1) CL2017000406A1 (en)
CO (1) CO2017001603A2 (en)
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RU2018145691A (en) 2013-01-23 2019-04-01 Альдейра Терапьютикс, Инк. DISEASES ASSOCIATED WITH TOXIC ALDEHYDE AND THEIR TREATMENT
WO2015155332A1 (en) 2014-04-11 2015-10-15 Boehringer Ingelheim International Gmbh Spiro[3h-indole-3,2'-pyrrolidin]-2(1h)-one derivatives and their use as mdm2-p53 inhibitors
EP3164401B1 (en) 2014-07-03 2018-12-26 Boehringer Ingelheim International GmbH New spiro[3h-indole-3,2´-pyrrolidin]-2(1h)-one compounds and derivatives as mdm2-p53 inhibitors
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