AR118729A1 - Inhibidor selectivo de la jak1 quinasa - Google Patents

Inhibidor selectivo de la jak1 quinasa

Info

Publication number
AR118729A1
AR118729A1 ARP200101101A ARP200101101A AR118729A1 AR 118729 A1 AR118729 A1 AR 118729A1 AR P200101101 A ARP200101101 A AR P200101101A AR P200101101 A ARP200101101 A AR P200101101A AR 118729 A1 AR118729 A1 AR 118729A1
Authority
AR
Argentina
Prior art keywords
alkyl
halogen
alkoxy
nrarb
hydroxyl
Prior art date
Application number
ARP200101101A
Other languages
English (en)
Inventor
Xiaolin Zhang
Zhenfan Yang
Qingbei Zeng
Honchung Tsui
changhe Qi
Original Assignee
Dizal Jiangsu Pharmaceutical Co Ltd
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 Dizal Jiangsu Pharmaceutical Co Ltd filed Critical Dizal Jiangsu Pharmaceutical Co Ltd
Publication of AR118729A1 publication Critical patent/AR118729A1/es

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Classifications

    • 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
    • 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
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Pulmonology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Immunology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicinal Preparation (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Compuestos de la fórmula (1), y sales farmacéuticamente aceptables de los mismos, que son de utilidad como inhibidores de JAK quinasa. También se divulgan composiciones farmacéuticas que comprenden uno o más compuestos de la fórmula (1), y métodos para utilizar dichos compuestos o composiciones en el tratamiento de condiciones respiratorias (por ejemplo, asma o EPOC). Reivindicación 1: Un compuesto caracterizado porque es de fórmula (1) o una sal farmacéuticamente aceptable del mismo, donde, el anillo A es un heteroarilo monocíclico o anillo bicíclico saturado o insaturado de 8 - 10 miembros que tiene 0 - 5 heteroátomos del anillo seleccionados entre oxígeno, azufre y nitrógeno, donde uno o más grupos -CH₂- que forman parte del heteroarilo, o el anillo bicíclico pueden reemplazarse por un grupo -C(O)-; R¹ es hidrógeno, halógeno, hidroxilo, amino, ciano, o C₁₋₃ alquilo; R² es hidrógeno, C₁₋₁₂ alquilo o C₁₋₁₂ alcoxilo opcionalmente sustituido en forma simple o múltiple con halógeno, hidroxilo, amino, ciano, o C₁₋₁₂ alcoxilo; cada uno de R³ y R⁴ en forma independiente está ausente, o es halógeno, hidroxilo, C₁₋₆ alquilo, carboxilo, C₁₋₆ alcoxilo, C₁₋₆ alcoxicarbonilo, -NRᵃRᵇ, -C(O)NRᵃRᵇ, sulfinilo, C₁₋₆ alquilsulfinilo, sulfonilo, C₁₋₆ alquilsulfonilo, sulfonoxilo, sulfoximinilo, C₁₋₆ alquilsulfoximinilo, sulfonimidoilo, S-(C₁₋₆ alquil)sulfonimidoilo, N-(C₁₋₆ alquil)sulfonimidoilo, N, S-(C₁₋₆ alquil)₂sulfonimidoilo, fosfinoilo, C₁₋₆ alquilfosfinoilo, (C₁₋₆ alquil)₂fosfinoilo, C₁₋₆ alquilfosfonilo, carbociclilo saturado o insaturado de 3 - 10 miembros, heterociclilo saturado o insaturado de 3 - 10 miembros, que puede estar opcionalmente sustituido en forma simple o múltiple en forma independiente con halógeno, hidroxilo, C₁₋₆ alquilo, C₁₋₆ alcoxilo, C₁₋₆ carboxilo, C₁₋₆ alcoxicarbonilo, -NRᵃRᵇ, -C(O)NRᵃRᵇ, sulfonilo, C₁₋₆ alquilsulfonilo, carbamoilo, N-(C₁₋₆ alquil)carbamoilo, o N,N-(C₁₋₆ alquil)₂carbamoilo, fosfinoilo, C₁₋₆ alquilfosfinoilo, (C₁₋₆ alquil)₂fosfinoilo, donde uno o más grupos -CH₂- que forman parte del carbociclilo o heterociclilo pueden reemplazarse por un grupo -C(O)-; donde, cada Rᵃ y Rᵇ se selecciona en forma independiente entre hidrógeno, C₁₋₆ alquilo, C₁₋₆ alquilcarbonilo, que puede estar opcionalmente sustituido en forma simple o múltiple en forma independiente con halógeno, hidroxilo, o C₁₋₆ alcoxi.
ARP200101101A 2019-04-19 2020-04-17 Inhibidor selectivo de la jak1 quinasa AR118729A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2019083376 2019-04-19

Publications (1)

Publication Number Publication Date
AR118729A1 true AR118729A1 (es) 2021-10-27

Family

ID=72837031

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP200101101A AR118729A1 (es) 2019-04-19 2020-04-17 Inhibidor selectivo de la jak1 quinasa

Country Status (12)

Country Link
US (1) US20220220096A1 (es)
EP (1) EP3956322A4 (es)
JP (1) JP2022529061A (es)
KR (1) KR20220003537A (es)
CN (1) CN113710664B (es)
AR (1) AR118729A1 (es)
AU (1) AU2020258619A1 (es)
BR (1) BR112021020964A2 (es)
CA (1) CA3134174A1 (es)
MX (1) MX2021012749A (es)
TW (1) TW202104215A (es)
WO (1) WO2020211839A1 (es)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2023551313A (ja) * 2020-11-26 2023-12-07 科輝智薬(深▲セン▼)新薬研究中心有限公司 アミド化合物、医薬組成物およびその使用
CN114380806B (zh) * 2022-03-24 2022-06-10 中国药科大学 2-氨基-4-吲哚基嘧啶类化合物及其制备方法与应用
US20240025884A1 (en) * 2022-07-05 2024-01-25 Dong-A St Co., Ltd. Compounds as gcn2 inhibitors, pharmaceutical compositions and uses thereof
WO2024013736A1 (en) * 2022-07-12 2024-01-18 Adama Makhteshim Ltd. Process for preparing substituted benzamides
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

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK3353168T3 (da) 2015-09-25 2023-10-02 Dizal Jiangsu Pharmaceutical Co Ltd Forbindelser og fremgangsmåder til at inhibere jak
CR20190332A (es) 2017-01-17 2019-09-13 Astrazeneca Ab Inhibidores selectivos de jak1
US20210371415A1 (en) * 2018-09-21 2021-12-02 Shanghai Ennovabio Pharmaceuticals Co., Ltd. Aromatic heterocyclic compound with kinase inhibitory activity

Also Published As

Publication number Publication date
WO2020211839A1 (en) 2020-10-22
CA3134174A1 (en) 2020-10-22
US20220220096A1 (en) 2022-07-14
CN113710664A (zh) 2021-11-26
AU2020258619A1 (en) 2021-09-16
EP3956322A1 (en) 2022-02-23
EP3956322A4 (en) 2023-05-03
JP2022529061A (ja) 2022-06-16
MX2021012749A (es) 2021-11-18
KR20220003537A (ko) 2022-01-10
BR112021020964A2 (pt) 2021-12-14
CN113710664B (zh) 2024-01-26
TW202104215A (zh) 2021-02-01

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