AR104642A1 - Compuestos carboximidamida derivados de bencimidazol e imidazopiridina - Google Patents

Compuestos carboximidamida derivados de bencimidazol e imidazopiridina

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Publication number
AR104642A1
AR104642A1 ARP160101418A ARP160101418A AR104642A1 AR 104642 A1 AR104642 A1 AR 104642A1 AR P160101418 A ARP160101418 A AR P160101418A AR P160101418 A ARP160101418 A AR P160101418A AR 104642 A1 AR104642 A1 AR 104642A1
Authority
AR
Argentina
Prior art keywords
alkyl
cycloalkyl
alkoxy
heterocyclyl
heteroaryl
Prior art date
Application number
ARP160101418A
Other languages
English (en)
Inventor
Van Veldhuizen Joshua
Sperandio David
Alissa Loyer-Drew Jennifer
Elbel Kristyna
Leigh Cosman Jennifer
Kenneth Corkey Britton
Andrew Codelli Julian
J Bartlett Mark
Yang Hai
Chung Yeung Suet
Original Assignee
Gilead Sciences Inc
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 Gilead Sciences Inc filed Critical Gilead Sciences Inc
Publication of AR104642A1 publication Critical patent/AR104642A1/es

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/4353—Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • A—HUMAN NECESSITIES
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    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/438—The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
    • A—HUMAN NECESSITIES
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    • A61K31/439—Heterocyclic 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 the ring forming part of a bridged ring system, e.g. quinuclidine
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    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non 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
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    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
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    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/472—Non-condensed isoquinolines, e.g. papaverine
    • A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
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    • A61K31/495—Heterocyclic 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
    • A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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    • A61K31/4965—Non-condensed pyrazines
    • A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
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    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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    • A61K31/535—Heterocyclic 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
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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Abstract

La presente se refiere a inhibidores de indolamina 2,3-dioxigenasa 1 (IDO1), además de las composiciones farmacéuticas que incluyen un compuesto de fórmula (1), o sus sales aceptables desde el punto de vista farmacéutico, y métodos de uso de los mismos para tratar enfermedades mediadas por IDO1. Reivindicación 1: Un compuesto de la fórmula (1) caracterizado porque R¹ es arilo o heteroarilo mono o bicíclico, en donde cada arilo o heteroarilo mono o bicíclico está sustituido en forma opcional con uno, dos o tres sustituyentes seleccionados en forma independiente de hidroxilo, halo; -CN, haloalquilo C₁₋₆, haloalcoxi C₁₋₆, alcoxi C₁₋₆, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, y cicloalquilo C₃₋₆, en donde dos de los sustituyentes opcionales pueden unirse para formar un anillo heterocíclico parcialmente saturado adicional; y en donde cada alcoxi C₁₋₆, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, y cicloalquilo C₃₋₆ está sustituido en forma opcional con uno, dos o tres sustituyentes seleccionados en forma independiente de hidroxilo, halo, -CN, -N(R²⁰)(R²²) y cicloalquilo C₃₋₆; X es N o CR²ᶜ; R²ᵃ, R²ᵇ, y R²ᶜ cada uno en forma independiente son hidrógeno, hidroxilo, halo, CN, haloalquilo C₁₋₆, haloalcoxi C₁₋₆, alcoxi C₁₋₆, o alquilo C₁₋₆; R²ᵈ y R²ᵉ son en forma independiente hidrógeno, haloalquilo C₁₋₆, haloalcoxi C₁₋₆, o alquilo C₁₋₆; n y m son en forma independiente 0, 1, 2, ó 3; cada Rⁿ y Rᵐ son en forma independiente hidrógeno, hidroxilo, halo, alcoxi C₁₋₆, alquilo C₁₋₆, cicloalquilo C₃₋₆, arilo, heterociclilo, o heteroarilo; o dos Rⁿ o Rᵐ se unen para formar un cicloalquilo C₃₋₆; y en donde cada alcoxi C₁₋₆, alquilo C₁₋₆, y cicloalquilarilo C₃₋₆, heterociclilo, o heteroarilo está sustituido en forma opcional con uno, dos o tres sustituyentes seleccionados en forma independiente de hidroxilo, halo, -CN, -N(R²⁰)(R²²), alquenilo C₂₋₆, alquinilo C₂₋₆, haloalquilo C₁₋₆, haloalcoxi C₁₋₆, alcoxi C₁₋₆, alquilo C₁₋₆, y cicloalquilo C₃₋₆; L es una unión, -NR³-, -C(O)-NR³-, -NR³-C(O)-, -NR³SO₂-, -NR³SO₂-NR³-, -SO₂NR³-, -O-, -S-, o -S(O)ₜ-, donde t es 0, 1 ó 2; cada R³ es en forma independiente hidrógeno, alquilo C₁₋₆, cicloalquilo C₃₋₆, arilo, heterociclilo, o heteroarilo; y Rᵗ es hidrógeno, alquilo C₁₋₆, alcoxi C₁₋₆, -C(O)R²⁰, -C(O)OR²⁰, -NC(O)OR²⁰, -N(R²⁰)(R²²), -C(O)N(R²⁰)(R²²), -SO₂R²⁰, -N(R²⁰)SO₂(R²¹), -N(R²⁰)SO₂-N(R²¹)(R²²), -SO₂N(R²⁰)(R²²), cicloalquilo C₃₋₁₅, arilo, heteroarilo, o heterociclilo, siempre que cuando Rᵗ alcoxi C₁₋₆, -NC(O)OR²⁰, -N(R²⁰)(R²²), -N(R²⁰)SO₂(R²¹), -N(R²⁰)SO₂-N(R²¹)(R²²), o - SO₂N(R²⁰)(R²²), y m es 0, entonces L sea una unión; en donde dicho alquilo C₁₋₆, alcoxi C₁₋₆, cicloalquilo C₃₋₁₅, arilo, heterociclilo, o heteroarilo está sustituido en forma opcional con uno, dos o tres sustituyentes seleccionados en forma independiente de hidroxilo, halo, -NO₂, haloalquilo C₁₋₆, haloalcoxi C₁₋₆, -C(O)R²⁰, -N(R²⁰)(R²²), -SO₂R²⁰, -N(R²⁰)SO₂(R²¹), -N(R²⁰)SO₂-N(R²¹)(R²²), -SO₂N(R²⁰)(R²²), cicloalquilo C₃₋₆, -CN, alcoxi C₁₋₆, alquilo C₁₋₆, y heterociclilo; y en donde dicho heterociclilo está sustituido en forma opcional con uno o dos oxo; en donde dicho cicloalquilo C₃₋₆, alquilo C₁₋₆ o alcoxi C₁₋₆ está sustituido en forma opcional con uno, dos o tres sustituyentes seleccionados en forma independiente de hidroxilo, halo, -NO₂, haloalquilo C₁₋₆, haloalcoxi C₁₋₆, alcoxi C₁₋₆, -N(R²⁰)(R²²), -SO₂R²⁰, -N(R²⁰)SO₂(R²²), -N(R²⁰)SO₂-N(R²¹)(R²²)-, y -SO₂N(R²⁰)(R²²); y dicho alquilo C₁₋₆ está sustituido en forma opcional con arilo; R²⁰, R²¹, y R²² se seleccionan en forma independiente de hidrógeno, alquilo C₁₋₆, haloalquilo C₁₋₆, cicloalquilo C₃₋₆, arilo, heterociclilo, y heteroarilo; en donde dichos arilo, heterociclilo o heteroarilo están sustituidos en forma opcional con uno, dos o tres halógenos; o una de sus sales, isómeros o mezclas de los anteriores aceptables desde el punto de vista farmacéutico.
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