AR121913A1 - Compuestos terapéuticos - Google Patents

Compuestos terapéuticos

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AR121913A1
AR121913A1 ARP210101081A ARP210101081A AR121913A1 AR 121913 A1 AR121913 A1 AR 121913A1 AR P210101081 A ARP210101081 A AR P210101081A AR P210101081 A ARP210101081 A AR P210101081A AR 121913 A1 AR121913 A1 AR 121913A1
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Argentina
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alkyl
cycloalkyl
heteroaryl
alkoxy
optionally substituted
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ARP210101081A
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English (en)
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Cathy Louise Lucas
Eileen Mary Seward
George Hynd
Emma Louise Blaney
Barrie Phillip Martin
Thorsten Nowak
Nicholas Charles Ray
Simon Ross Crumpler
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C4X Discovery Ltd
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Publication of AR121913A1 publication Critical patent/AR121913A1/es

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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/472Non-condensed isoquinolines, e.g. papaverine
    • A61K31/4725Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
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    • 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
    • A61K31/501Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
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    • A61K31/00Medicinal preparations containing organic active ingredients
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    • 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
    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
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    • AHUMAN NECESSITIES
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    • AHUMAN NECESSITIES
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    • 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
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • 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
    • C07D401/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
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    • 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
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    • 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
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    • 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
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    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04Ortho-condensed systems

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
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  • Obesity (AREA)
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  • Dermatology (AREA)
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  • Heart & Thoracic Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

La presente invención se refiere a compuestos que son activadores de Nrf2. Los compuestos tienen la fórmula estructural (1) que se define en la presente. La presente invención también se refiere a procesos para la preparación de estos compuestos, a composiciones que los comprenden y a su uso en el tratamiento de enfermedades o trastornos asociados con la activación de Nrf2. Reivindicación 1: Un compuesto según la fórmula (1) o la fórmula (2), o una sal farmacéuticamente aceptable de este, caracterizado porque: R¹ se selecciona entre alquileno-R¹¹ C₁₋₄, heterociclilo y heteroarilo bicíclico de 8 a 10 miembros, donde dicho heterociclilo está opcionalmente sustituido con uno o más sustituyentes independientemente seleccionados de alquilo C₁₋₄, -C(O)-R¹², alquileno-OR¹⁴ C₁₋₃, SO₂-R¹³ y heteroarilo que está opcionalmente sustituido con uno o más sustituyentes independientemente seleccionados de alquilo C₁₋₄, cicloalquilo C₃₋₇, halo, OH, alcoxi C₁₋₃ y ciano; y donde dicho heteroarilo bicíclico de 8 - 10 miembros está opcionalmente sustituido con uno o más sustituyentes independientemente seleccionados de alquilo C₁₋₄, cicloalquilo C₃₋₇, halo, OH y alcoxi C₁₋₃; R² se selecciona entre hidrógeno, fluoro, cloro y alquilo C₁₋₃; R³ se selecciona entre hidrógeno, fluoro, cloro, bromo, alcoxi C₁₋₃, alquilo C₁₋₃, haloalquilo C₁₋₃ y ciano; R⁴ es hidrógeno o alquilo C₁₋₄; R⁵ es alquilo -C(O)-C₁₋₄, cicloalquilo -C(O)-C₃₋₇, heteroarilo-C(O)- o arilo-C(O)-, donde dicho heteroarilo y arilo están opcionalmente sustituidos con uno o más sustituyentes seleccionados de alquilo C₁₋₄, halo, hidroxi, alcoxi C₁₋₃, CO₂R¹⁵ y ciano; o R⁴ y R⁵, tomados junto con el átomo de nitrógeno al que se acoplan, de un anillo heterociclilo de 4, 5 ó 6 miembros, donde dicho anillo heterociclilo comprende una o más mitades -C(O)- acopladas al átomo de nitrógeno; opcionalmente contiene uno o más heteroátomos adicionales seleccionados del oxígeno, del nitrógeno y del azufre; opcionalmente está fusionado a un anillo arilo o heteroarilo; opcionalmente está acoplado en espiral a un grupo cicloalquilo C₃₋₇ o a un anillo heterociclilo de 3 a 6 miembros; y opcionalmente está sustituido por uno o más sustituyentes seleccionados de alquilo C₁₋₄, halo, OH, alcoxi C₁₋₃, haloalquilo C₁₋₃, ciano, NR¹⁶R¹⁷, C(O)R¹⁸, S(O)R¹⁹ y SO₂R²⁰; R⁶ se selecciona entre hidrógeno, alquilo C₁₋₄ y cicloalquilo C₃₋₇; R⁸ es C(=O)NR⁸ᵃR⁸ᵇ o -C(=O)R⁸ᶜ; R⁸ᵃ es hidrógeno o alquilo C₁₋₆; R⁸ᵇ es hidrógeno, alquilo C₁₋₆ o cicloalquilo C₃₋₇, donde los grupos alquilo C₁₋₆ o cicloalquilo C₃₋₇ están opcionalmente sustituidos con uno o más sustituyentes seleccionados de alquilo C₁₋₄, cicloalquilo C₃₋₇, halo, OH, alcoxi C₁₋₃, haloalquilo C₁₋₃, ciano, NR¹⁶R¹⁷, C(O)R¹⁸, S(O)R¹⁹ y SO₂R²⁰; o R⁸ᵃ y R⁸ᵇ, en conjunto con el átomo de nitrógeno al que están adheridos, forman un anillo heterocíclico de 3, 4, 5, 6 ó 7 miembros: opcionalmente contienen uno o más heteroátomos adicionales seleccionados del oxígeno, nitrógeno y azufre; y se sustituye opcionalmente con uno o más sustituyentes seleccionados de forma independiente de C₁₋₄alquil, C₃₋₇cicloalquil, halo, OH, C₁₋₃alcoxi, C₁₋₃haloalquil, ciano, NR¹⁶R¹⁷, C(O)R¹⁸, S(O)R¹⁹ y SO₂R²⁰; R⁸ᶜ es alquilo C₁₋₃, o haloalquilo C₁₋₃; R⁹ es metilo; R¹¹ se selecciona entre -C(O)-R²⁴, -SO₂-R²⁵, -NR²⁶C(O)-R²⁷, -NR²⁸SO₂-R²⁹, heterociclilo, arilo y heteroarilo, donde dichos grupos arilo y heteroarilo están opcionalmente sustituidos con uno o más sustituyentes seleccionados de alquilo C₁₋₄, haloalquilo C₁₋₃, cicloalquilo C₃₋₇, alquileno-R³⁰ C₁₋₄, halo, OH, alcoxi C₁₋₃, heterociclilo y ciano; y dicho heterociclilo está opcionalmente sustituido con uno o más sustituyentes independientemente seleccionados de alquilo C₁₋₄, haloalquilo C₁₋₃, cicloalquilo C₃₋₇, alquileno-R³⁰ C₁₋₄, halo, OH, alcoxi C₁₋₃, oxo y ciano; R¹² se selecciona entre alquilo C₁₋₄, cicloalquilo C₃₋₇, OR³¹, NR³²R³³, arilo y heteroarilo, donde dichos arilo y heteroarilo están opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados de alquilo C₁₋₄, halo, OH, alcoxi C₁₋₃ y ciano; R¹³ se selecciona entre alquilo C₁₋₄, cicloalquilo C₃₋₇, heteroarilo, heterociclilo y NR³⁴R³⁵, donde dichos heteroarilo y heterociclilo están opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados de alquilo C₁₋₄, halo, OH, alcoxi C₁₋₃ y ciano; R¹⁷ se selecciona entre hidrógeno, alquilo C₁₋₄, alquilo C(O)C₁₋₃ y C(O)NR³⁶R³⁷; R¹⁸, R¹⁹ y R²⁰ se seleccionan independientemente de alquilo C₁₋₄, OH, alcoxi C₁₋₃ y NR³⁸R³⁹; R²⁴ se selecciona entre alquilo C₁₋₄, NR⁴⁰R⁴¹ y OR⁴²; R²⁵ se selecciona entre alquilo C₁₋₄ y NR⁴³R⁴⁴; R²⁷ se selecciona entre alquilo C₁₋₄, cicloalquilo C₃₋₇, haloalquilo C₁₋₃, heterociclilo, arilo y heteroarilo, donde dichos arilo y heteroarilo están opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados de alquilo C₁₋₄, haloalquilo C₁₋₃, cicloalquilo C₃₋₇, alquileno-R⁴⁵ C₁₋₄, halo, OH, alcoxi C₁₋₃ y ciano; R²⁹ se selecciona entre alquilo C₁₋₄, cicloalquilo C₃₋₇, haloalquilo C₁₋₃, arilo y heteroarilo, donde dichos arilo y heteroarilo están opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados de alquilo C₁₋₄, haloalquilo C₁₋₃, cicloalquilo C₃₋₇, alquileno-R⁴⁶ C₁₋₄, halo, OH, alcoxi C₁₋₃ y ciano; R³⁰ se selecciona entre hidroxi, alquilo C₁₋₃, cicloalquilo C₃₋₇, ciano y NR⁴⁷R⁴⁸; R⁴⁰ se selecciona entre manera de hidrógeno y alquilo C₁₋₄; R⁴¹ se selecciona entre hidrógeno, alquilo C₁₋₄, cicloalquilo C₃₋₇, alcoxi C₁₋₃, arilo y heteroarilo; o R⁴⁰ y R⁴¹, tomados junto con el átomo de nitrógeno al que se acoplan, de un anillo heteroarilo o heterociclilo de 4, 5 ó 6 miembros, donde dichos anillos heteroarilo o heterociclilo están opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados de alquilo C₁₋₄, halo, OH, alcoxi C₁₋₃, C₃₋₇cicloalquilo y ciano; R⁴⁵ y R⁴⁶ se seleccionan independientemente de hidroxi, alcoxi C₁₋₃ y cicloalquilo C₃₋₇; y R¹⁴, R¹⁵, R¹⁶, R²⁶, R²⁸, R³¹, R³², R³³, R³⁴, R³⁵, R³⁶, R³⁷, R³⁸, R³⁹, R⁴², R⁴³, R⁴⁴, R⁴⁷ y R⁴⁸ se seleccionan independientemente de hidrógeno, alquilo C₁₋₄ y cicloalquilo C₃₋₇; siempre que el compuesto no sea (1S,2R)-2-((S)-5-cloro-8-((5-(difluorometil)-1-metil-1H-1,2,3-triazol-4-il)metoxi)-1-((2-oxopirrolidin-1-il)metil)-1,2,3,4-tetrahidroisoquinolina-2-carbonil)-1-metilciclohexano-1-carboxamida.
ARP210101081A 2020-04-22 2021-04-22 Compuestos terapéuticos AR121913A1 (es)

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CN (1) CN115667242A (es)
AR (1) AR121913A1 (es)
AU (1) AU2021258539A1 (es)
BR (1) BR112022021370A2 (es)
CA (1) CA3174360A1 (es)
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ES2963613T3 (es) * 2018-10-22 2024-04-01 C4X Discovery Ltd Compuestos terapéuticos
WO2023073364A1 (en) 2021-10-25 2023-05-04 C4X Discovery Limited Tetrahydroisoquinoline compounds that are keap1 binders

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US20140256767A1 (en) * 2011-10-31 2014-09-11 The Broad Institute, Inc. Direct inhibitors of keap1-nrf2 interaction as antioxidant inflammation modulators
RU2018101077A (ru) * 2015-06-15 2019-07-15 Глэксосмитклайн Интеллекчуал Проперти Дивелопмент Лимитед Регуляторы nrf2
JP2020097526A (ja) * 2017-03-28 2020-06-25 武田薬品工業株式会社 複素環化合物
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