AR123962A1 - Inhibidores de interleucina-17 - Google Patents

Inhibidores de interleucina-17

Info

Publication number
AR123962A1
AR123962A1 ARP210103016A ARP210103016A AR123962A1 AR 123962 A1 AR123962 A1 AR 123962A1 AR P210103016 A ARP210103016 A AR P210103016A AR P210103016 A ARP210103016 A AR P210103016A AR 123962 A1 AR123962 A1 AR 123962A1
Authority
AR
Argentina
Prior art keywords
alkyl
substituted
unsubstituted
cycloalkyl
phenyl
Prior art date
Application number
ARP210103016A
Other languages
English (en)
Inventor
Thomas Josef Troxler
David Orain
Pascal Furet
Klaus Weigand
Achim Schlapbach
Original Assignee
Novartis Ag
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 Novartis Ag filed Critical Novartis Ag
Publication of AR123962A1 publication Critical patent/AR123962A1/es

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Classifications

    • 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
    • C07D401/02Heterocyclic 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 two hetero rings
    • C07D401/12Heterocyclic 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 two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/443Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/02Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • 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
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • 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
    • C07D405/02Heterocyclic 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 two hetero rings
    • C07D405/12Heterocyclic 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 two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • C07D417/02Heterocyclic 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 two hetero rings
    • C07D417/12Heterocyclic 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 two hetero rings linked by a chain containing hetero atoms as chain links
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Immunology (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

La presente invención se refiere a nuevos compuestos de 2-formamido (N-fenil y N-piridil) acetamida sustituidos con N-óxidos de piridina que son inhibidores de interleucina-17 (IL-17), a procesos para su preparación, composiciones farmacéuticas, y medicamentos que los contienen, y a su uso en enfermedades y trastornos mediados por IL-17. Reivindicación 1: Un compuesto de la fórmula [1] en donde, R¹ es un compuesto de fórmula [2] ó [3] en donde, R⁶ en cada ocurrencia se selecciona entre H, F, Cl, alquilo C₁₋₃ y fluoroalquilo C₁₋₃; R⁷ en cada ocurrencia se selecciona entre H, F, Cl, alquilo C₁₋₃ y fluoroalquilo C₁₋₃; R⁸ se selecciona entre H, halo, alquilo C₁₋₃ e hidroximetilo; X es C o N y cuando X es N, R³ está ausente; R² se selecciona entre H y F; R³ se selecciona entre H, F y Cl; R⁴ se selecciona entre H y F; R⁵ es un heteroarilo de 5 miembros que comprende 1 ó 2 heteroátomos independientemente seleccionados entre N, S, y O, y en donde dicho heteroarilo es insustituido o sustituido con uno o dos grupos independientemente seleccionados entre alquilo C₁₋₃ y cicloalquilo C₃₋₄, en donde dicho alquilo C₁₋₃ es insustituido o sustituido con uno o más grupos independientemente seleccionados entre F, OH, alcoxi C₁₋₃, -C(O)OH y NR¹ᵇR¹ᶜ, en donde R¹ᵇ y R¹ᶜ son independientemente seleccionados entre H y alquilo C₁₋₃; o R⁵ es un heteroarilo de 5 miembros que comprende un átomo de N en donde dicho heteroarilo de 5 miembros se fusiona a un heterociclo de 6 miembros que comprende un átomo de N en donde dicho heterociclo es insustituido o sustituido con un grupo seleccionado entre alquilo C₁₋₃, alcoxi C₁₋₃ alquilo C₁₋₃, -C(O)alquilo C₁₋₃, cicloalquilo C₃₋₄ y oxetanilo; Z es un resto de fórmula [4], en donde R⁹ se selecciona entre (1) cicloalquilo C₅₋₈ monocíclico y bicicloalquilo C₆, cada uno de los cuales es independientemente insustituido o sustituido con uno o más grupos independientemente seleccionados en cada ocurrencia entre fluoro, alquilo C₁₋₃ y fluoroalquilo C₁₋₃, y en donde dicho cicloalquilo C₅₋₈ monocíclico está opcionalmente fusionado a fenilo; en donde dicho fenilo es insustituido o sustituido con uno o más grupos seleccionados entre halo, alquilo C₁₋₃, cicloalquilo C₃₋₅ o fluoroalquilo C₁₋₃; (2) cicloalquenilo C₅₋₈ monocíclico, que es insustituido o sustituido con uno o más fluoro; (3) alquilo C₁₋₃, que es insustituido o sustituido con uno o dos grupos fenilo, en donde dicho fenilo en cada ocurrencia es independientemente insustituido o sustituido con uno o más halo; o una sal farmacéuticamente aceptable del mismo.
ARP210103016A 2020-11-02 2021-10-29 Inhibidores de interleucina-17 AR123962A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP20205121 2020-11-02

Publications (1)

Publication Number Publication Date
AR123962A1 true AR123962A1 (es) 2023-01-25

Family

ID=73059405

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP210103016A AR123962A1 (es) 2020-11-02 2021-10-29 Inhibidores de interleucina-17

Country Status (19)

Country Link
US (1) US20230391782A1 (es)
EP (1) EP4237417A1 (es)
JP (1) JP2023547470A (es)
KR (1) KR20230091945A (es)
CN (1) CN116323596A (es)
AR (1) AR123962A1 (es)
AU (1) AU2021368247B2 (es)
CA (1) CA3190738A1 (es)
CL (1) CL2023001220A1 (es)
CO (1) CO2023005280A2 (es)
CR (1) CR20230180A (es)
DO (1) DOP2023000081A (es)
EC (1) ECSP23030375A (es)
IL (1) IL302447A (es)
MX (1) MX2023005076A (es)
PE (1) PE20231047A1 (es)
TW (1) TW202227408A (es)
UY (1) UY39484A (es)
WO (1) WO2022091056A1 (es)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023025783A1 (en) 2021-08-23 2023-03-02 Leo Pharma A/S Small molecule modulators of il-17
WO2023111181A1 (en) 2021-12-16 2023-06-22 Leo Pharma A/S Small molecule modulators of il-17
WO2023166172A1 (en) 2022-03-04 2023-09-07 Leo Pharma A/S Small molecule modulators of il-17
WO2024115662A1 (en) 2022-12-02 2024-06-06 Leo Pharma A/S Small molecule modulators of il-17

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6562333B1 (en) 1993-06-14 2003-05-13 Schering Corporation Purified mammalian CTLA-8 antigens and related reagents
US20050070567A1 (en) 2002-08-12 2005-03-31 The Regents Of The University Of Michigan Diagnosis and treatment of diseases arising from defects in the tuberous sclerosis pathway
GB0417487D0 (en) 2004-08-05 2004-09-08 Novartis Ag Organic compound
JP6347949B2 (ja) 2010-04-26 2018-06-27 ノバルティス アーゲー 改良型細胞培養培地
WO2013116682A1 (en) 2012-02-02 2013-08-08 Ensemble Therapeutics Corporation Macrocyclic compounds for modulating il-17
US20150252028A1 (en) 2012-10-24 2015-09-10 Bristol-Myers Squibb Company Hepatitis c virus inhibitors
WO2014066726A2 (en) 2012-10-26 2014-05-01 Ensemble Therapeutics Corporation Compounds for modulating il-17
KR101877109B1 (ko) 2013-02-08 2018-07-10 노파르티스 아게 항-il-17a 항체 및 자가면역 및 염증성 장애의 치료에서의 그의 용도
MA42032A (fr) 2015-02-02 2018-03-14 Forma Therapeutics Inc Acides 3-aryl-4-amido-bicyclo [4,5,0]hydroxamiques en tant qu'inhibiteurs de hdac
MX2021006421A (es) 2018-12-19 2021-08-16 Leo Pharma As Anilidas de aminoácidos como moduladores de moléculas pequeñas de interleucinas-17 (il-17).

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DOP2023000081A (es) 2023-06-15
JP2023547470A (ja) 2023-11-10
KR20230091945A (ko) 2023-06-23
AU2021368247A9 (en) 2023-10-05
MX2023005076A (es) 2023-05-16
CA3190738A1 (en) 2022-05-05
UY39484A (es) 2022-06-30
CR20230180A (es) 2023-05-25
AU2021368247B2 (en) 2023-10-05
TW202227408A (zh) 2022-07-16
IL302447A (en) 2023-06-01
CN116323596A (zh) 2023-06-23
CO2023005280A2 (es) 2023-05-19
CL2023001220A1 (es) 2023-12-22
AU2021368247A1 (en) 2023-05-18
PE20231047A1 (es) 2023-07-11
ECSP23030375A (es) 2023-05-31
US20230391782A1 (en) 2023-12-07
EP4237417A1 (en) 2023-09-06
WO2022091056A1 (en) 2022-05-05

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