CR20190310A - Compuestos de pirazolopirimidina y métodos de uso de los mismos - Google Patents

Compuestos de pirazolopirimidina y métodos de uso de los mismos

Info

Publication number
CR20190310A
CR20190310A CR20190310A CR20190310A CR20190310A CR 20190310 A CR20190310 A CR 20190310A CR 20190310 A CR20190310 A CR 20190310A CR 20190310 A CR20190310 A CR 20190310A CR 20190310 A CR20190310 A CR 20190310A
Authority
CR
Costa Rica
Prior art keywords
methods
pyrazolopyrimidine compounds
compounds
kinase inhibitors
pyrazolopyrimidine
Prior art date
Application number
CR20190310A
Other languages
English (en)
Inventor
Yun-Xing Cheng
Guiling Zhao
F Anthony Romero
Paul Gibbons
Limin Cheng
Po-Wai Yuen
Mark Zak
Wei Li
Original Assignee
Hoffmann La Roche
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
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of CR20190310A publication Critical patent/CR20190310A/es

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic 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
    • C07D487/04—Ortho-condensed systems
    • 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
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/10—Spiro-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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

En el presente documento se describen compuestos de fórmula (IA) o una sal farmacéuticamente aceptable de los mismos y métodos de uso como inhibidores de Janus cinasa.Compounds of Formula (IA), or a pharmaceutically acceptable salt thereof, and methods of use as Janus kinase inhibitors are described herein.
CR20190310A 2016-12-29 2017-12-22 Compuestos de pirazolopirimidina y métodos de uso de los mismos CR20190310A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN2016112932 2016-12-29
PCT/EP2017/084569 WO2018122212A1 (en) 2016-12-29 2017-12-22 Pyrazolopyrimidine compounds and methods of use thereof

Publications (1)

Publication Number Publication Date
CR20190310A true CR20190310A (es) 2019-08-21

Family

ID=61094385

Family Applications (1)

Application Number Title Priority Date Filing Date
CR20190310A CR20190310A (es) 2016-12-29 2017-12-22 Compuestos de pirazolopirimidina y métodos de uso de los mismos

Country Status (19)

Country Link
US (1) US11155557B2 (es)
EP (1) EP3562809B1 (es)
JP (1) JP6900491B2 (es)
KR (1) KR20190100337A (es)
CN (1) CN110114343B (es)
AU (1) AU2017385543A1 (es)
BR (1) BR112019013287A2 (es)
CA (1) CA3046435A1 (es)
CL (1) CL2019001694A1 (es)
CO (1) CO2019006220A2 (es)
CR (1) CR20190310A (es)
IL (1) IL267671A (es)
MA (1) MA47167A (es)
MX (1) MX2019007339A (es)
PE (1) PE20191236A1 (es)
PH (1) PH12019501022A1 (es)
RU (1) RU2019123319A (es)
UA (1) UA122851C2 (es)
WO (1) WO2018122212A1 (es)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2017385543A1 (en) 2016-12-29 2019-05-23 F. Hoffmann-La Roche Ag Pyrazolopyrimidine compounds and methods of use thereof
WO2018215389A1 (en) 2017-05-22 2018-11-29 F. Hoffmann-La Roche Ag Therapeutic compounds and compositions, and methods of use thereof
JP7339263B2 (ja) * 2018-01-15 2023-09-05 エフ． ホフマン－ラ ロシュ アーゲー Ｊａｋ阻害剤としてのピラゾロピリミジン化合物
EP3986899A1 (en) * 2019-06-18 2022-04-27 F. Hoffmann-La Roche AG Pyrazolopyrimidine aryl ether inhibitors of jak kinases and uses thereof
MX2021015319A (es) 2019-06-18 2022-04-07 Hoffmann La Roche Inhibidores de jak cinasas basados en pirazolopirimidina sulfona y usos de los mismos.
US20200399274A1 (en) * 2019-06-18 2020-12-24 Genentech, Inc. Tetrazole-substituted pyrazolopyrimidine inhibitors of jak kinases and uses thereof
WO2022175829A1 (en) * 2021-02-17 2022-08-25 Cellix Bio Private Limited Topical formulations and compositions
EP4583977A1 (en) * 2022-09-09 2025-07-16 Chiesi Farmaceutici S.p.A. Heterocyclic derivatives as janus kinase inhibitors
IL319348A (en) * 2022-09-09 2025-05-01 Chiesi Farm Spa History of heterocyclics as Janus kinase inhibitors

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU650953B2 (en) 1991-03-21 1994-07-07 Novartis Ag Inhaler
US5543523A (en) 1994-11-15 1996-08-06 Regents Of The University Of Minnesota Method and intermediates for the synthesis of korupensamines
EP0842195A1 (en) 1995-07-06 1998-05-20 Zeneca Limited Peptide inhibitors of fibronectine
US6248713B1 (en) 1995-07-11 2001-06-19 Biogen, Inc. Cell adhesion inhibitors
YU25500A (sh) 1999-05-11 2003-08-29 Pfizer Products Inc. Postupak za sintezu analoga nukleozida
GB0028383D0 (en) 2000-11-21 2001-01-03 Novartis Ag Organic compounds
EP1241176A1 (en) 2001-03-16 2002-09-18 Pfizer Products Inc. Purine derivatives for the treatment of ischemia
CA2470813A1 (en) 2001-12-20 2003-07-03 Bayer Healthcare Ag 1,4-dihydro-1,4-diphenylpyridine derivatives
SE0302487D0 (sv) 2003-09-18 2003-09-18 Astrazeneca Ab Novel compounds
GB0502258D0 (en) 2005-02-03 2005-03-09 Argenta Discovery Ltd Compounds and their use
CN102127078A (zh) 2005-07-14 2011-07-20 安斯泰来制药株式会社 Janus激酶3的杂环类抑制剂
KR20110033223A (ko) 2008-06-20 2011-03-30 제넨테크, 인크. 트리아졸로피리딘 ｊａｋ 억제제 화합물 및 방법
UA110324C2 (en) * 2009-07-02 2015-12-25 Genentech Inc Jak inhibitory compounds based on pyrazolo pyrimidine
US8575336B2 (en) 2011-07-27 2013-11-05 Pfizer Limited Indazoles
EA032488B1 (ru) * 2014-05-23 2019-06-28 Ф. Хоффманн-Ля Рош Аг Соединения 5-хлор-дифторметоксифенилпиразолопиримидина, представляющие собой ингибиторы янус-киназы
TW201720828A (zh) 2015-11-23 2017-06-16 赫孚孟拉羅股份公司 治療性化合物及組合物以及其使用方法
JP6936236B2 (ja) 2016-02-18 2021-09-15 エフ．ホフマン−ラ ロシュ アーゲーＦ． Ｈｏｆｆｍａｎｎ−Ｌａ Ｒｏｃｈｅ Ａｋｔｉｅｎｇｅｓｅｌｌｓｃｈａｆｔ 治療化合物、組成物及びその方法の使用
SG11201811697SA (en) 2016-06-29 2019-01-30 Hanmi Pharmaceutical Co Ltd Glucagon derivative, conjugate thereof, composition comprising same and therapeutic use thereof
AU2017385543A1 (en) 2016-12-29 2019-05-23 F. Hoffmann-La Roche Ag Pyrazolopyrimidine compounds and methods of use thereof

Also Published As

Publication number Publication date
CL2019001694A1 (es) 2019-11-22
KR20190100337A (ko) 2019-08-28
MA47167A (fr) 2019-11-06
BR112019013287A2 (pt) 2019-12-24
US11155557B2 (en) 2021-10-26
RU2019123319A (ru) 2021-02-01
PE20191236A1 (es) 2019-09-11
WO2018122212A1 (en) 2018-07-05
AU2017385543A1 (en) 2019-05-23
CA3046435A1 (en) 2018-07-05
CN110114343A (zh) 2019-08-09
UA122851C2 (uk) 2021-01-06
CN110114343B (zh) 2022-09-06
CO2019006220A2 (es) 2019-06-28
EP3562809A1 (en) 2019-11-06
JP6900491B2 (ja) 2021-07-07
RU2019123319A3 (es) 2021-02-01
JP2020503339A (ja) 2020-01-30
IL267671A (en) 2019-08-29
PH12019501022A1 (en) 2019-12-16
US20190345165A1 (en) 2019-11-14
MX2019007339A (es) 2019-09-06
EP3562809B1 (en) 2021-06-09

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