PE20180279A1 - Derivados de 2-(pirazolopiridin-3-il)pirimidina como inhibidores de jak - Google Patents

Derivados de 2-(pirazolopiridin-3-il)pirimidina como inhibidores de jak

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Publication number
PE20180279A1
PE20180279A1 PE2017002479A PE2017002479A PE20180279A1 PE 20180279 A1 PE20180279 A1 PE 20180279A1 PE 2017002479 A PE2017002479 A PE 2017002479A PE 2017002479 A PE2017002479 A PE 2017002479A PE 20180279 A1 PE20180279 A1 PE 20180279A1
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Prior art keywords
pyrazolopyridin
compounds
ylpyrimidin
pyrazolo
pyridin
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PE2017002479A
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English (en)
Inventor
Trias Cristina Esteve
Moll Joan Taltavull
Rodriguez Jacob Gonzalez
Juan Bernat Vidal
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Almirall Sa
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Publication of PE20180279A1 publication Critical patent/PE20180279A1/es

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    • 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
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    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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    • 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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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
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    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members

Abstract

Referido a derivados de 2-(pirazolopiridin-3-il)pirimidina, de formula I, en donde: X es O, NR3; R1 y R2 son H, halogeno, alquilo C1-C4, alcoxilo C1-C4, CN; G1 es CN, CORa, OR6, entre otros. Estos compuestos son inhibidores de cinasa Janus (JAK). Entre los compuestos preferidos tenemos los siguientes: (trans-4-{[5-fluoro-6-(4-hidroxipiperidin-1-il)-2-pirazolo[1,5-a]piridin-3-ilpirimidin-4-il]amino}ciclohexil)acetonitrilo; (trans-4-{[6(4-aminopiperidin-1-il)-5-fluoro-2-pirazolo[1,5-a]piridin-3-ilpirimidin-4-il]amino}ciclohexil)acetonitrilo, entre otros. Estos compuestos se pueden emplear en el tratamiento de diversas enfermedades o estados patologicos como trastornos neurologicos, enfermedad cardiovascular, dolor, rechazo de trasplante de medula osea y de organos, sindrome mielodisplasico, cancer, leucemia, linfoma, dermatitis atopica, eccema, vitiligo, entre otras.
PE2017002479A 2015-06-11 2016-06-10 Derivados de 2-(pirazolopiridin-3-il)pirimidina como inhibidores de jak PE20180279A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP15382305 2015-06-11

Publications (1)

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PE20180279A1 true PE20180279A1 (es) 2018-02-07

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US (1) US10759793B2 (es)
EP (1) EP3307272A1 (es)
JP (1) JP2018516954A (es)
KR (1) KR20180012854A (es)
CN (1) CN107667106A (es)
AR (1) AR104963A1 (es)
AU (1) AU2016275716C1 (es)
BR (1) BR112017025781A2 (es)
CA (1) CA2987328A1 (es)
CL (1) CL2017003107A1 (es)
CO (1) CO2017011996A2 (es)
CR (1) CR20170557A (es)
EA (1) EA035312B1 (es)
HK (1) HK1246667A1 (es)
IL (1) IL255668A (es)
MA (1) MA42592A (es)
MX (1) MX2017015029A (es)
PE (1) PE20180279A1 (es)
PH (1) PH12017502236A1 (es)
SG (1) SG10201911926UA (es)
TW (1) TW201705961A (es)
WO (1) WO2016198663A1 (es)

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BR112018003741A2 (pt) 2015-08-24 2018-09-25 Glaxosmithkline Ip No 2 Ltd composições biofarmacêuticas
US20190029987A1 (en) * 2016-02-12 2019-01-31 Universitat Zurich Dimethyl fumarate (dmf) for prevention or treatment of gout, acne, diabetes, vitiligo and/or pyoderma gangrenosum
US11020396B2 (en) 2016-11-08 2021-06-01 Cancer Research Technology Limited Pyrimidinone derivatives as Cdc7 inhibitors
WO2018136554A1 (en) * 2017-01-17 2018-07-26 Menlo Therapeutics Inc. Use of neurokinin-1 antagonists as antitussives
US11311548B2 (en) 2017-03-02 2022-04-26 Aslan Pharmaceuticals Pte. Ltd. Cancer therapy
TW201834649A (zh) * 2017-03-02 2018-10-01 新加坡商亞獅康私人有限公司 癌症療法
US11957931B2 (en) * 2017-04-26 2024-04-16 Yale University Compositions and methods for treating vitiligo
CN108514637A (zh) * 2018-05-07 2018-09-11 山东省眼科研究所 Stat3抑制剂s31-201在治疗干眼症中的应用
CN109810991B (zh) * 2019-03-02 2021-11-12 昆明理工大学 二氢蝶酸合酶基因folP的用途
CA3177477A1 (en) * 2020-06-02 2021-12-09 Nerre Therapeutics Limited Neurokinin (nk)-1 receptor antagonists for use in the treatment of pulmonary fibrosis conditions promoted by mechanical injury to the lungs
CA3219092A1 (en) * 2021-05-03 2022-11-10 Incyte Corporation Jak1 pathway inhibitors for the treatment of prurigo nodularis

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JPS54128591A (en) 1978-03-25 1979-10-05 Kyowa Hakko Kogyo Co Ltd Cephalosporin analog
EP2338888A1 (en) 2009-12-24 2011-06-29 Almirall, S.A. Imidazopyridine derivatives as JAK inhibitors
UY33213A (es) * 2010-02-18 2011-09-30 Almirall Sa Derivados de pirazol como inhibidores de jak
EP2397482A1 (en) 2010-06-15 2011-12-21 Almirall, S.A. Heteroaryl imidazolone derivatives as jak inhibitors
AR086042A1 (es) * 2011-04-28 2013-11-13 Galapagos Nv Compuesto util para el tratamiento de enfermedades degenerativas e inflamatorias y composicion farmaceutica
WO2013025628A1 (en) * 2011-08-15 2013-02-21 Ligand Pharmaceuticals Incorporated Janus kinase inhibitor compounds and methods
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TW201605811A (zh) * 2013-12-11 2016-02-16 阿爾米雷爾有限公司 作為jak抑制劑之吡唑并嘧啶-2基衍生物

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AU2016275716B2 (en) 2020-01-23
EP3307272A1 (en) 2018-04-18
CR20170557A (es) 2018-02-06
WO2016198663A1 (en) 2016-12-15
US20180162856A1 (en) 2018-06-14
KR20180012854A (ko) 2018-02-06
JP2018516954A (ja) 2018-06-28
MA42592A (fr) 2018-06-20
IL255668A (en) 2018-01-31
EA201792689A1 (ru) 2018-07-31
SG10201911926UA (en) 2020-01-30
MX2017015029A (es) 2018-04-13
TW201705961A (zh) 2017-02-16
PH12017502236A1 (en) 2018-06-11
AR104963A1 (es) 2017-08-30
AU2016275716C1 (en) 2020-10-15
CL2017003107A1 (es) 2018-04-02
US10759793B2 (en) 2020-09-01
HK1246667A1 (zh) 2018-09-14
NZ737314A (en) 2021-02-26
BR112017025781A2 (pt) 2018-08-14
CN107667106A (zh) 2018-02-06
CO2017011996A2 (es) 2018-03-28
CA2987328A1 (en) 2016-12-15
EA035312B1 (ru) 2020-05-27
AU2016275716A1 (en) 2017-12-07

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