PE20191108A1 - Inhibidores selectivos de jak1 - Google Patents

Inhibidores selectivos de jak1

Info

Publication number
PE20191108A1
PE20191108A1 PE2019001401A PE2019001401A PE20191108A1 PE 20191108 A1 PE20191108 A1 PE 20191108A1 PE 2019001401 A PE2019001401 A PE 2019001401A PE 2019001401 A PE2019001401 A PE 2019001401A PE 20191108 A1 PE20191108 A1 PE 20191108A1
Authority
PE
Peru
Prior art keywords
methyl
fluoro
ethyl
selective inhibitors
methylpyrimidin
Prior art date
Application number
PE2019001401A
Other languages
English (en)
Inventor
Qibin Su
Karl Magnus Nilsson
Annika Birgitta Margareta Åstrand
Anna Ingrid Kristina Berggren
Johan R Johansson
Sameer Pralhad Kawatkar
Jason Grant Kettle
Matti Juhani Lepisto
Original Assignee
Astrazeneca Ab
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 Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of PE20191108A1 publication Critical patent/PE20191108A1/es

Links

Classifications

    • 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/007Pulmonary tract; Aromatherapy
    • A61K9/0073Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy
    • A61K9/0075Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy for inhalation via a dry powder inhaler [DPI], e.g. comprising micronized drug mixed with lactose carrier particles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/14Drugs for dermatological disorders for baldness or alopecia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Dermatology (AREA)
  • Immunology (AREA)
  • Epidemiology (AREA)
  • Diabetes (AREA)
  • Otolaryngology (AREA)
  • Pulmonology (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

La presente invencion se refiere a un compuesto de formula I y sales aceptables del mismo, donde: R1, R3, y R4 son individualmente hidrogeno o metilo; R2 es hidrogeno, metilo o -CH2CH2OH; n es 1 o 2; R5 es metilo, etilo o -CH 2OR8; R6 es metilo, cloro o fluor; R7 es metilo, etilo y ciclopropilo; y R8 es metilo, etilo o bencilo. Son compuestos preferidos: (R) -N- (3- (2 - ((2-fluoro-3- (metilsulfonil) fenil) amino) -5-metilpirimidin-4-il) -1H- indol-7-il) -2- (4 - (2-hidroxietil) piperazin-1-il) propanamida; (R) -N- (3- (2- (2-fluoro-3- (metilsulfonil) fenilamino) -5-metilpirimidin-4-il) -1H- indol-7-il) -2- (4-metilpiperazina-1-il) propanamida; entre otros. Tambien se refiere a una composicion farmaceutica. Dichos compuestos son inhibidores selectivos de la cinasa asociada a Janus (JAK1) utiles en el tratamiento de leucemia, linfoma, entre otros.
PE2019001401A 2017-01-17 2018-01-16 Inhibidores selectivos de jak1 PE20191108A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201762447057P 2017-01-17 2017-01-17
PCT/EP2018/051038 WO2018134213A1 (en) 2017-01-17 2018-01-16 Jak1 selective inhibitors

Publications (1)

Publication Number Publication Date
PE20191108A1 true PE20191108A1 (es) 2019-08-26

Family

ID=61024756

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2019001401A PE20191108A1 (es) 2017-01-17 2018-01-16 Inhibidores selectivos de jak1

Country Status (37)

Country Link
US (2) US10961228B2 (es)
EP (2) EP3571192B1 (es)
JP (3) JP6986086B2 (es)
KR (2) KR102659213B1 (es)
CN (2) CN110461830B (es)
AR (1) AR110753A1 (es)
AU (1) AU2018209667B2 (es)
BR (1) BR112019014526A2 (es)
CA (1) CA3049175A1 (es)
CL (1) CL2019001993A1 (es)
CO (1) CO2019007888A2 (es)
CR (1) CR20190332A (es)
DK (1) DK3571192T3 (es)
DO (1) DOP2019000184A (es)
EA (1) EA037067B1 (es)
EC (1) ECSP19051352A (es)
ES (1) ES2938648T3 (es)
FI (1) FI3571192T3 (es)
HR (1) HRP20230069T1 (es)
HU (1) HUE061064T2 (es)
IL (1) IL267851B (es)
JO (1) JOP20190174B1 (es)
LT (1) LT3571192T (es)
MA (1) MA47301B1 (es)
MX (2) MX2019008435A (es)
NI (1) NI201900077A (es)
PE (1) PE20191108A1 (es)
PH (1) PH12019501639A1 (es)
PL (1) PL3571192T3 (es)
PT (1) PT3571192T (es)
RS (1) RS63981B1 (es)
SG (1) SG11201906222WA (es)
SI (1) SI3571192T1 (es)
TW (1) TWI753089B (es)
UA (1) UA124246C2 (es)
WO (1) WO2018134213A1 (es)
ZA (1) ZA201906875B (es)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102659213B1 (ko) * 2017-01-17 2024-04-18 아스트라제네카 아베 Jak1 선택적 억제제
KR101954369B1 (ko) * 2017-01-26 2019-03-05 한미약품 주식회사 피리미딘 화합물 및 그의 의약 용도
MA53162A (fr) * 2018-07-18 2021-05-26 Astrazeneca Ab Sel de xinafoate d'un composé inhibiteur de jak
KR102669660B1 (ko) * 2018-09-21 2024-05-27 상하이 엔노바바이오 파마슈티컬스 씨오 엘티디. 키나아제 억제 활성을 가진 방향족 헤테로고리 화합물
CA3134174A1 (en) 2019-04-19 2020-10-22 Dizal (Jiangsu) Pharmaceutical Co., Ltd. Jak1 selective kinase inhibitor
JP7478252B2 (ja) * 2020-04-09 2024-05-02 ディスアーム セラピューティクス, インコーポレイテッド Sarm1の阻害剤
US20240025884A1 (en) * 2022-07-05 2024-01-25 Dong-A St Co., Ltd. Compounds as gcn2 inhibitors, pharmaceutical compositions and uses thereof
CN115260128B (zh) * 2022-09-21 2022-12-09 苏州凯瑞医药科技有限公司 一种新型jak抑制剂关键中间体的制备方法
CN115974845A (zh) * 2023-01-19 2023-04-18 奥锐特药业股份有限公司 奥希替尼中间体的制备方法

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW200626559A (en) * 2004-10-13 2006-08-01 Wyeth Corp Anilino-pyrimidine analogs
CN101421250A (zh) * 2006-01-30 2009-04-29 埃克塞里艾克西斯公司 作为jak-2调节剂的4-芳基-2-氨基-嘧啶或4-芳基-2-氨基烷基-嘧啶及包含它们的药物组合物
WO2009046416A1 (en) * 2007-10-05 2009-04-09 Targegen Inc. Anilinopyrimidines as jak kinase inhibitors
GB0805477D0 (en) * 2008-03-26 2008-04-30 Univ Nottingham Pyrimidines triazines and their use as pharmaceutical agents
UA110324C2 (en) * 2009-07-02 2015-12-25 Genentech Inc Jak inhibitory compounds based on pyrazolo pyrimidine
EP4036088B1 (en) 2010-03-10 2024-04-03 Incyte Holdings Corporation Piperidin-4-yl azetidine derivatives as jak1 inhibitors
BR112013006016A2 (pt) * 2010-09-15 2016-06-07 Hoffmann La Roche compostos de azabenzotiazol, composições e métodos de uso
US20150118229A1 (en) 2013-10-24 2015-04-30 Abbvie Inc. Jak1 selective inhibitor and uses thereof
EP4219482A1 (en) * 2015-09-25 2023-08-02 Dizal (Jiangsu) Pharmaceutical Co., Ltd. Compounds and methods for inhibiting jak
KR102659213B1 (ko) * 2017-01-17 2024-04-18 아스트라제네카 아베 Jak1 선택적 억제제

Also Published As

Publication number Publication date
EA201991700A1 (ru) 2020-01-28
TWI753089B (zh) 2022-01-21
IL267851B (en) 2021-08-31
EA037067B1 (ru) 2021-02-02
ES2938648T3 (es) 2023-04-13
HUE061064T2 (hu) 2023-05-28
IL267851A (en) 2019-09-26
CO2019007888A2 (es) 2019-07-31
CN110461830B (zh) 2022-11-01
BR112019014526A2 (pt) 2020-02-27
HRP20230069T1 (hr) 2023-03-17
AU2018209667A1 (en) 2019-08-22
KR20190104215A (ko) 2019-09-06
US20210188821A1 (en) 2021-06-24
CN110461830A (zh) 2019-11-15
DOP2019000184A (es) 2019-08-15
NI201900077A (es) 2020-03-18
MA47301A (fr) 2019-11-27
JP2022043059A (ja) 2022-03-15
PL3571192T3 (pl) 2023-03-20
US20190367490A1 (en) 2019-12-05
AU2018209667B2 (en) 2020-05-07
CR20190332A (es) 2019-09-13
US10961228B2 (en) 2021-03-30
PH12019501639A1 (en) 2020-07-06
AR110753A1 (es) 2019-05-02
MX2019008435A (es) 2019-09-09
EP3571192A1 (en) 2019-11-27
ZA201906875B (en) 2021-05-26
RS63981B1 (sr) 2023-03-31
MX2022002976A (es) 2022-04-06
LT3571192T (lt) 2023-02-27
KR102659213B1 (ko) 2024-04-18
JP6986086B2 (ja) 2021-12-22
EP3571192B1 (en) 2022-11-30
WO2018134213A1 (en) 2018-07-26
MA47301B1 (fr) 2023-02-28
TW201838984A (zh) 2018-11-01
KR102585048B1 (ko) 2023-10-05
JP7394820B2 (ja) 2023-12-08
DK3571192T3 (da) 2023-02-06
PT3571192T (pt) 2023-02-21
UA124246C2 (uk) 2021-08-11
SG11201906222WA (en) 2019-08-27
JP2024010041A (ja) 2024-01-23
CA3049175A1 (en) 2018-07-26
JOP20190174B1 (ar) 2023-09-17
CN115925693A (zh) 2023-04-07
FI3571192T3 (fi) 2023-03-06
ECSP19051352A (es) 2019-07-31
KR20230141938A (ko) 2023-10-10
CL2019001993A1 (es) 2019-12-27
US11897869B2 (en) 2024-02-13
JP2020506171A (ja) 2020-02-27
SI3571192T1 (sl) 2023-03-31
JOP20190174A1 (ar) 2019-07-14
EP4219470A1 (en) 2023-08-02

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