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PE20190632A1 - Compuestos 8-(azetidin-1-il)-[1,2,4]triazolo[1,5-a]piridinilo, composiciones y metodos de utilizacion de los mismos - Google Patents

Compuestos 8-(azetidin-1-il)-[1,2,4]triazolo[1,5-a]piridinilo, composiciones y metodos de utilizacion de los mismos

Info

Publication number
PE20190632A1
PE20190632A1 PE2019000482A PE2019000482A PE20190632A1 PE 20190632 A1 PE20190632 A1 PE 20190632A1 PE 2019000482 A PE2019000482 A PE 2019000482A PE 2019000482 A PE2019000482 A PE 2019000482A PE 20190632 A1 PE20190632 A1 PE 20190632A1
Authority
PE
Peru
Prior art keywords
azetidin
compounds
piridinyl
triazolo
pirazol
Prior art date
Application number
PE2019000482A
Other languages
English (en)
Inventor
Mark Zak
Simon Charles Goodacre
Limin Cheng
F Anthony Romero
Yun-Xing Cheng
Rongbao Hua
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 PE20190632A1 publication Critical patent/PE20190632A1/es

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
    • A61K31/435Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic 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)
  • Pulmonology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

SE REFIERE A COMPUESTOS 8-(AZETIDIN-1-IL)-[1,2,4]TRIAZOLO[1,5-A]PIRIDINILO DE FORMULA (I) O (II) DONDE EL ANILLO A ES FENILO, PIRIDINILO, PIRAZOLILO O ISOQUINOLINILO; EL ANILLO B ES FENILO O HETEROARILO DE 5-6 ELEMENTOS; n ES 0, 1 O 2; R2 ES -C(O)-NH-(ALQUILO C1-C6 SUSTITUIDO OPCIONALMENTE CON HALOGENO, OH O CN), ENTRE OTROS; R3, R4 Y R5 SON CADA UNO H, CH3, CH2CH3, ENTRE OTROS; R6 ES H O ALQUILO C1-C3; R1a ES HALOGENO, ALQUILO C1-C6 SUSTITUIDO OPCIONALMENTE CON HALOGENO, CN O OH, ALCOXI C1-C6, ENTRE OTROS; R1b Y R1c JUNTOS FORMAN UN HETEROCICLOALQUILO DE 3 A 10 ELEMENTOS SUSTITUIDO OPCIONALMENTE CON ALQUILO C1-C6, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 2-[3-(4-ETIL-1H-PIRAZOL-1-IL)-1-[2-([1-[2-(4-METILPIPERAZIN-1-IL)-2-OXOETIL]-1H-PIRAZOL-4-IL]AMINO)-[1,2,4]TRIAZOLO[1,5-a]PIRIDIN-8-IL]AZETIDIN-3-IL]ACETONITRILO; 2-[3-(4,4-DIFLUORO-1-PIPERIDIL)-1-[2-[[1-[2-(4-METILPIPERAZIN-1-IL)-2-OXO-ETIL]PIRAZOL-4-IL]AMINO]-[1,2,4]TRIAZOLO[1,5-a]PIRIDIN-8-IL]AZETIDIN-3-IL]ACETONITRILO; ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LAS QUINASAS DE JANUS (JAK) SIENDO UTILES EN EL TRATAMIENTO DE ASMA
PE2019000482A 2016-09-06 2017-09-02 Compuestos 8-(azetidin-1-il)-[1,2,4]triazolo[1,5-a]piridinilo, composiciones y metodos de utilizacion de los mismos PE20190632A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2016098215 2016-09-06

Publications (1)

Publication Number Publication Date
PE20190632A1 true PE20190632A1 (es) 2019-04-26

Family

ID=59761965

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2019000482A PE20190632A1 (es) 2016-09-06 2017-09-02 Compuestos 8-(azetidin-1-il)-[1,2,4]triazolo[1,5-a]piridinilo, composiciones y metodos de utilizacion de los mismos

Country Status (19)

Country Link
US (3) US20190202822A1 (es)
EP (2) EP4198036A1 (es)
JP (1) JP7050761B2 (es)
KR (1) KR20190045302A (es)
CN (1) CN109890817B (es)
AU (1) AU2017324281A1 (es)
BR (1) BR112019004486A2 (es)
CA (1) CA3035712A1 (es)
CL (1) CL2019000568A1 (es)
CO (1) CO2019002171A2 (es)
CR (1) CR20190118A (es)
IL (1) IL265153A (es)
MA (1) MA46176A (es)
MX (1) MX2019002627A (es)
PE (1) PE20190632A1 (es)
PH (1) PH12019500478A1 (es)
RU (1) RU2019109570A (es)
SG (1) SG11201901954XA (es)
WO (1) WO2018046409A1 (es)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114008050A (zh) * 2019-06-18 2022-02-01 豪夫迈·罗氏有限公司 Jak激酶的吡唑并嘧啶芳基醚抑制剂及其用途
GB202213164D0 (en) 2022-09-08 2022-10-26 Cambridge Entpr Ltd Novel compounds, compositions and therapeutic uses thereof
WO2024148184A1 (en) * 2023-01-04 2024-07-11 Aerie Pharmaceuticals, Inc. Compounds and processes for the preparation of jak inhibitors
WO2024148186A1 (en) * 2023-01-04 2024-07-11 Aerie Pharmaceuticals, Inc. Polymorphs of a jak1/tyk2 inhibitor and uses thereof

Family Cites Families (17)

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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
WO1997002289A1 (en) 1995-07-06 1997-01-23 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
JP4486817B2 (ja) 2001-12-20 2010-06-23 バイエル・シェーリング・ファルマ・アクチェンゲゼルシャフト 1,4−ジヒドロ−1,4−ジフェニルピリジン誘導体
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
EP2288260A4 (en) * 2008-06-20 2013-10-23 Genentech Inc TRIAZOLOPYRIDINE-JAK HEMMER COMPOUNDS AND METHOD
WO2010010184A1 (en) * 2008-07-25 2010-01-28 Galapagos Nv [1, 2, 4] triazolo [1, 5-a] pyridines as jak inhibitors
MX2011012961A (es) 2009-06-05 2012-01-30 Cephalon Inc Preparacion y usos de derivados de 1,2,4-triazolo[1,5a]-piridina.
US8575336B2 (en) 2011-07-27 2013-11-05 Pfizer Limited Indazoles
RS61482B1 (sr) * 2013-05-17 2021-03-31 Incyte Corp Derivati bipirazola kao inhibitori jak
EP3041841B1 (en) 2013-09-05 2019-06-05 F. Hoffmann-La Roche AG Triazolopyridine compounds, compositions and methods of use thereof
EP3265464A1 (en) * 2015-03-04 2018-01-10 F. Hoffmann-La Roche AG Triazolopyridine compounds and methods of use thereof

Also Published As

Publication number Publication date
US20230242530A1 (en) 2023-08-03
CR20190118A (es) 2019-04-30
MA46176A (fr) 2019-07-17
CN109890817B (zh) 2022-06-17
CO2019002171A2 (es) 2019-05-21
PH12019500478A1 (en) 2019-12-02
WO2018046409A1 (en) 2018-03-15
SG11201901954XA (en) 2019-04-29
EP3510030B1 (en) 2023-03-22
RU2019109570A (ru) 2020-10-08
CL2019000568A1 (es) 2019-07-12
US20190202822A1 (en) 2019-07-04
US20200270248A1 (en) 2020-08-27
BR112019004486A2 (pt) 2019-05-28
CN109890817A (zh) 2019-06-14
MX2019002627A (es) 2019-10-30
KR20190045302A (ko) 2019-05-02
RU2019109570A3 (es) 2020-10-08
JP7050761B2 (ja) 2022-04-08
JP2019526593A (ja) 2019-09-19
IL265153A (en) 2019-05-30
EP4198036A1 (en) 2023-06-21
AU2017324281A1 (en) 2019-03-21
CA3035712A1 (en) 2018-03-15
EP3510030A1 (en) 2019-07-17

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