AR089182A1 - Derivados de aminopirimidina como moduladores de lrrk2 - Google Patents

Derivados de aminopirimidina como moduladores de lrrk2

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AR089182A1
AR089182A1 ARP120104438A ARP120104438A AR089182A1 AR 089182 A1 AR089182 A1 AR 089182A1 AR P120104438 A ARP120104438 A AR P120104438A AR P120104438 A ARP120104438 A AR P120104438A AR 089182 A1 AR089182 A1 AR 089182A1
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Argentina
Prior art keywords
alkyl
cycloalkyl
optionally substituted
halogen
alkoxy
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ARP120104438A
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English (en)
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Gunzner-Toste Janet
Baker-Glenn Charles
Jon Burdick Daniel
Chambers Mark
K Chan Bryan
Chen Huifen
Estrada Anthony
Shore Daniel
Sweeney Zachary
Wang Shumei
Zhao Guiling
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Hoffmann La Roche
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Publication of AR089182A1 publication Critical patent/AR089182A1/es

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    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
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    • 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
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    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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    • 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
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
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    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
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  • 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

Los compuestos son útiles para el tratamiento de enfermedades asociadas con el receptor de la LRRK2, por ejemplo la enfermedad de Parkinson. Reivindicación 1: Compuestos de la fórmula (1) o sales farmacéuticamente aceptables de los mismos, en la que: m es un número de 0 a 3; X es: -NRᵃ-; -O-; o -S(O)ʳ-, en el que r es un número de 0 a 2 y Rᵃ es hidrógeno o alquilo C₁₋₆; R¹ es: alquilo C₁₋₆; alquenilo C₂₋₆; alquinilo C₂₋₆; haloalquilo C₁₋₆; (alcoxi C₁₋₆)-alquilo C₁₋₆; hidroxi-alquilo C₁₋₆; amino-alquilo C₁₋₆; (alquilsulfonil C₁₋₆)-alquilo C₁₋₆; cicloalquilo C₃₋₆ opcionalmente sustituido por alquilo C₁₋₆ o halógeno; (cicloalquil C₃₋₆)-alquilo C₁₋₆, cuya porción cicloalquilo C₃₋₆ está opcionalmente sustituida por alquilo C₁₋₆; tetrahidropiranilo; tetrahidrofuranilo; tetrahidrofuranil-alquilo C₁₋₆; oxetanilo; u oxetanil-alquilo C₁₋₆; o R¹ y Rᵃ junto con los átomos, a los que están unidos, pueden formar un anillo de tres a seis eslabones que opcionalmente puede incluir un heteroátomo adicional elegido entre O, N y S, y que está sustituido por oxo, halógeno o alquilo C₁₋₆; R² es: halógeno; alcoxi C₁₋₆; ciano; alquinilo C₂₋₆; alquenilo C₂₋₆; haloalquilo C₁₋₆; halo-alcoxi C₁₋₆; cicloalquilo C₃₋₆, cuya porción cicloalquilo C₃₋₆ está opcionalmente sustituida por alquilo C₁₋₆; (cicloalquil C₃₋₆)-alquilo C₁₋₆, cuya porción cicloalquilo C₃₋₆ está opcionalmente sustituida por alquilo C₁₋₆; tetrahidrofuranilo; tetrahidrofuranil-alquilo C₁₋₆; acetilo; oxetanilo; u oxetanil-alquilo C₁₋₆; R³ᵃ es: -OR⁴; halógeno; ciano; alquilo C₁₋₆; haloalquilo C₁₋₆; cicloalquilo C₃₋₆ opcionalmente sustituido por alquilo C₁₋₆; (cicloalquil C₃₋₆)-alquilo C₁₋₆, cuya porción cicloalquilo C₃₋₆ está opcionalmente sustituida por alquilo C₁₋₆; tetrahidrofuranilo; tetrahidrofuranil-alquilo C₁₋₆; oxetanilo; u oxetanil-alquilo C₁₋₆; R³ᵇ es: hidrógeno, o R³ᵃ y R³ᵇ junto con los átomos, a los que están unidos, pueden formar un anillo de cinco o seis eslabones, que incluye opcionalmente uno o dos heteroátomos, cada uno de ellos se elige con independencia entre O, N y S, dicho anillo está opcionalmente sustituido una o varias veces por R⁸; R⁴ es: hidrógeno; alquilo C₁₋₆; haloalquilo C₁₋₆; (alcoxi C₁₋₆)-alquilo C₁₋₆; cicloalquilo C₃₋₆ opcionalmente sustituido por alquilo C₁₋₆ o halógeno; (cicloalquil C₃₋₆)-alquilo C₁₋₆, cuya porción cicloalquilo C₃₋₆ está opcionalmente sustituida por alquilo C₁₋₆ o halógeno; tetrahidrofuranilo; tetrahidrofuranil-alquilo C₁₋₆; oxetanilo; u oxetanil-alquilo C₁₋₆; R⁵ es: hidrógeno; o alquilo C₁₋₆; R⁶ es: hidrógeno; alquilo C₁₋₆; (alcoxi C₁₋₆)-alquilo C₁₋₆; hidroxi-alquilo C₁₋₆; amino-alquilo C₁₋₆; cicloalquilo C₃₋₆; (cicloalquil C₃₋₆)-alquilo C₁₋₆; heteroarilo, heterociclilo; o heterociclil-alquilo C₁₋₆; dichos cicloalquilo C₃₋₆, (cicloalquil C₃₋₆)-alquilo C₁₋₆, heteroarilo, heterociclilo y heterociclil-alquilo C₁₋₆ pueden estar en cada caso opcionalmente sustituidos por uno, dos, tres o cuatro grupos elegidos con independencia entre: alquilo C₁₋₆; haloalquilo C₁₋₆; alcoxi C₁₋₆; halo-alcoxi C₁₋₆; hidroxi; hidroxi-alquilo C₁₋₆; halógeno; nitrilo; (alquil C₁₋₆)-carbonilo; (alquil C₁₋₆)-sulfonilo; cicloalquilo C₃₋₆; (cicloalquil C₃₋₆)-alquilo C₁₋₆; (cicloalquil C₃₋₆)-carbonilo; amino; y heterociclilo; o dos de los grupos junto con los átomos, a los que están unidos, pueden formar un anillo de cinco o seis eslabones; o R⁵ y R⁶ junto con el átomo de nitrógeno al que están unidos forman un anillo de tres a siete eslabones, que opcionalmente incluye un heteroátomo adicional elegido entre O, N y S(O)ₙ, y que está opcionalmente sustituido por uno, dos, tres o cuatro grupos elegidos con independencia entre: alquilo C₁₋₆; haloalquilo C₁₋₆; alcoxi C₁₋₆; halo-alcoxi C₁₋₆; hidroxi; (alcoxi C₁₋₆)-alquilo C₁₋₆; hidroxi-alquilo C₁₋₆; halógeno, nitrilo; (alquil C₁₋₆)-carbonilo; (alquil C₁₋₆)-sulfonilo; cicloalquilo C₃₋₆; (cicloalquil C₃₋₆)-alquilo C₁₋₆; (cicloalquil C₃₋₆)-carbonilo; amino; o heterociclilo; o dos de los grupos junto con los átomos, a los que están unidos, pueden formar un anillo de cinco o seis eslabones; y R⁷ es: halógeno; alquilo C₁₋₆; alcoxi C₁₋₆; haloalquilo C₁₋₆; o halo-alcoxi C₁₋₆; R⁸ es: halógeno; alquilo C₁₋₆; u oxo.
ARP120104438A 2011-11-29 2012-11-27 Derivados de aminopirimidina como moduladores de lrrk2 AR089182A1 (es)

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RU2661197C2 (ru) 2018-07-13
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