MX2023006816A - Derivados de n-(imidazo)[1,2-b]piridazin-3-il)-1-ciclohexil-2h-ind azol-5-carboxamida y de n-(pirazolo[1,5-a]pirimidin-3-il)-1-cicloh exil-2h-indazol-5-carboxamida como inhibidores de irak4 para el tratamiento del asma. - Google Patents

Derivados de n-(imidazo)[1,2-b]piridazin-3-il)-1-ciclohexil-2h-ind azol-5-carboxamida y de n-(pirazolo[1,5-a]pirimidin-3-il)-1-cicloh exil-2h-indazol-5-carboxamida como inhibidores de irak4 para el tratamiento del asma.

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Publication number
MX2023006816A
MX2023006816A MX2023006816A MX2023006816A MX2023006816A MX 2023006816 A MX2023006816 A MX 2023006816A MX 2023006816 A MX2023006816 A MX 2023006816A MX 2023006816 A MX2023006816 A MX 2023006816A MX 2023006816 A MX2023006816 A MX 2023006816A
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Mexico
Prior art keywords
cyclohexyl
indazole
formula
pyridazin
imidazo
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MX2023006816A
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English (en)
Inventor
Anna Ingrid Kristina Berggren
Ina Terstiege
Stefan Schiesser
Yafeng Xue
Hui-Fang Chang
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Astrazeneca Ab
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Publication of MX2023006816A publication Critical patent/MX2023006816A/es

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-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
    • A61K31/495Heterocyclic 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/5025Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring 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
    • A61K31/495Heterocyclic 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
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • 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
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • 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]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Pulmonology (AREA)
  • Dermatology (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Transplantation (AREA)
  • Epidemiology (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

La presente solicitud se refiere a un compuesto de Fórmula (A), en donde R1 se selecciona entre la Fórmula (II) y Fórmula (III) y R2 se selecciona entre la Fórmula (IV), Fórmula (V) y Fórmula (VI) como inhibidores de IRAK4 para su uso en métodos de tratamiento de, por ejemplo, asma y enfermedad pulmonar obstructiva crónica (EPOC), cáncer, enfermedades inflamatorias y enfermedades autoinflamatorias/autoinmunitarias tales como, por ejemplo, el lupus eritematoso sistémico, artritis reumatoide, miositis, síndrome de Sjögren, esclerosis sistémica, gota, endometriosis, dermatitis atópica y psoriasis. Los compuestos preferidos de la presente invención son, por ejemplo: derivados de ? N-(imidazo[1,2-b]piridazin-3-il)-1-ciclohexil-2H-indazol-5-ca rboxamida, ? N-(pirazolo[1,5-a]pirimidin-3-il)-1-ciclohexil-2H-ind azol-5-carboxamida, ? N-(imidazo[1,2-b]piridazin-3-il)-1-azaespiro [4.5]decan-8-il-2H-indazol-5-carboxamida y ? N-(pirazolo[1,5-a]pir imidin-3-il)-1-azaespiro[4.5]decan-8-il-2H-indazol-5-carboxamida. Un compuesto de ejemplo de la presente invención es, por ejemplo, N-(imidazo[1,2-b]piridazin-3-il)-6-metoxi-2-((5r,8r)-1-metil-2-ox o-1-azaespiro[4.5]decan-8-il)-2H-indazol-5-carboxamida (Ejemplo 1): Fórmula (VII). (ver Fórmulas).
MX2023006816A 2020-12-10 2021-12-09 Derivados de n-(imidazo)[1,2-b]piridazin-3-il)-1-ciclohexil-2h-ind azol-5-carboxamida y de n-(pirazolo[1,5-a]pirimidin-3-il)-1-cicloh exil-2h-indazol-5-carboxamida como inhibidores de irak4 para el tratamiento del asma. MX2023006816A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US202063199160P 2020-12-10 2020-12-10
PCT/EP2021/084916 WO2022122876A1 (en) 2020-12-10 2021-12-09 N-(imidazo[1,2-b]pyridazin-3-yl)-1-cyclohexyl-2h-indazole-5-carboxamide and n-(pyrazolo[1,5-a]pyrimidin-3-yl)-1-cyclohexyl-2h-indazole-5-carboxamide derivatives as irak4 inhibitors for the treatment of asthma

Publications (1)

Publication Number Publication Date
MX2023006816A true MX2023006816A (es) 2023-06-21

Family

ID=79230946

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Application Number Title Priority Date Filing Date
MX2023006816A MX2023006816A (es) 2020-12-10 2021-12-09 Derivados de n-(imidazo)[1,2-b]piridazin-3-il)-1-ciclohexil-2h-ind azol-5-carboxamida y de n-(pirazolo[1,5-a]pirimidin-3-il)-1-cicloh exil-2h-indazol-5-carboxamida como inhibidores de irak4 para el tratamiento del asma.

Country Status (20)

Country Link
US (1) US11866405B2 (es)
EP (1) EP4259632A1 (es)
JP (1) JP2023552838A (es)
KR (1) KR20230118153A (es)
CN (1) CN116583285A (es)
AR (1) AR124303A1 (es)
AU (1) AU2021395816B2 (es)
CA (1) CA3203569A1 (es)
CL (1) CL2023001662A1 (es)
CO (1) CO2023007624A2 (es)
CR (1) CR20230264A (es)
DO (1) DOP2023000119A (es)
EC (1) ECSP23050553A (es)
IL (1) IL303356A (es)
MX (1) MX2023006816A (es)
PE (1) PE20240684A1 (es)
TW (1) TW202237612A (es)
UY (1) UY39561A (es)
WO (1) WO2022122876A1 (es)
ZA (1) ZA202306848B (es)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023152349A1 (en) * 2022-02-14 2023-08-17 Astrazeneca Ab Irak4 inhibitors
WO2023227703A1 (en) * 2022-05-26 2023-11-30 Astrazeneca Ab Solid forms of heterocyclylamides as irak4 inhibitors

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2604062C2 (ru) 2010-07-13 2016-12-10 Ф.Хоффманн-Ля Рош Аг ПРОИЗВОДНЫЕ ПИРАЗОЛО[1,5-a]ПИРИМИДИНА И ТИЕНО[3,2-b]ПИРИМИДИНА В КАЧЕСТВЕ МОДУЛЯТОРОВ IRAK-4
US9073892B2 (en) 2010-12-20 2015-07-07 Merck Serono S.A. Indazolyl triazol derivatives
CA2903490C (en) 2013-03-15 2021-04-13 Biomarin Pharmaceutical Inc. Hdac inhibitors
SG11201605408RA (en) 2014-01-10 2016-07-28 Aurigene Discovery Tech Ltd Indazole compounds as irak4 inhibitors
EA032559B1 (ru) 2014-04-04 2019-06-28 Пфайзер Инк. Бициклические аннелированные гетероарильные или арильные соединения и их применение в качестве ингибиторов irak4
JO3705B1 (ar) 2014-11-26 2021-01-31 Bayer Pharma AG إندازولات مستبدلة جديدة، عمليات لتحضيرها، مستحضرات دوائية تحتوي عليها واستخدامها في إنتاج أدوية
WO2016174183A1 (en) 2015-04-30 2016-11-03 Bayer Pharma Aktiengesellschaft Combinations of inhibitors of irak4 with inhibitors of btk
AU2016293446A1 (en) 2015-07-15 2018-02-15 Aurigene Discovery Technologies Limited Substituted aza compounds as IRAK-4 inhibitors
BR112018000624A2 (pt) 2015-07-15 2018-09-18 Aurigene Discovery Technologies Limited compostos de indazol e azaindazol como inibidores de irak-4
CA3016364A1 (en) 2016-03-03 2017-09-08 Bayer Pharma Aktiengesellschaft New 2-substituted indazoles, methods for producing same, pharmaceutical preparations that contain same, and use of same to produce drugs
US10059708B2 (en) 2016-04-26 2018-08-28 Northwestern University Therapeutic targeting of the interleukin 1 receptor-associated kinase 4 (IRAK4) in leukemias characterized by rearrangements in the mixed lineage leukemia gene (MLL-r)
BR112018074919A2 (pt) 2016-06-01 2020-11-03 Bayer Pharma Aktiengesellschaft uso de indazóis 2-substituídos para tratamento e profilaxia de doenças autoimunes.
CN110770229A (zh) 2017-06-21 2020-02-07 豪夫迈·罗氏有限公司 作为irak4调节剂的苯并呋喃化合物
EP3642201A1 (en) 2017-06-21 2020-04-29 H. Hoffnabb-La Roche Ag Isoindolinone derivatives as irak4 modulators
EP3990454A1 (en) 2019-06-27 2022-05-04 Biogen MA Inc. Imidazo[1,2-a]pyridinyl derivatives and their use in the treatment of disease
BR112021026369A2 (pt) 2019-06-27 2022-05-17 Biogen Ma Inc Derivados de 2h-indazol e seu uso no tratamento de doenças

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Publication number Publication date
EP4259632A1 (en) 2023-10-18
IL303356A (en) 2023-08-01
JP2023552838A (ja) 2023-12-19
US11866405B2 (en) 2024-01-09
US20220185817A1 (en) 2022-06-16
AU2021395816B2 (en) 2024-04-04
CN116583285A (zh) 2023-08-11
UY39561A (es) 2022-06-30
WO2022122876A1 (en) 2022-06-16
DOP2023000119A (es) 2023-07-09
ECSP23050553A (es) 2023-08-31
PE20240684A1 (es) 2024-04-10
AR124303A1 (es) 2023-03-15
CL2023001662A1 (es) 2024-01-12
ZA202306848B (en) 2024-04-24
CA3203569A1 (en) 2022-06-16
AU2021395816A1 (en) 2023-07-13
CO2023007624A2 (es) 2023-06-30
CR20230264A (es) 2023-07-26
TW202237612A (zh) 2022-10-01
KR20230118153A (ko) 2023-08-10

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