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AR097086A1 - Derivados 1,3-disustituidos de ciclopentano - Google Patents

Derivados 1,3-disustituidos de ciclopentano

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Publication number
AR097086A1
AR097086A1 ARP140102798A ARP140102798A AR097086A1 AR 097086 A1 AR097086 A1 AR 097086A1 AR P140102798 A ARP140102798 A AR P140102798A AR P140102798 A ARP140102798 A AR P140102798A AR 097086 A1 AR097086 A1 AR 097086A1
Authority
AR
Argentina
Prior art keywords
denotes
atoms
hal
substituted
mono
Prior art date
Application number
ARP140102798A
Other languages
English (en)
Inventor
Dr Tsaklakidis Christos
Dr Staehle Wolfgang
Dr Leuthner Birgitta
Original Assignee
Merck Patent Ges Mit Beschränkter Haftung
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 Merck Patent Ges Mit Beschränkter Haftung filed Critical Merck Patent Ges Mit Beschränkter Haftung
Publication of AR097086A1 publication Critical patent/AR097086A1/es

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • C07D233/61—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms not forming part of a nitro radical, attached to ring nitrogen atoms
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—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
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    • 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
    • A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
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    • 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
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  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Son inhibidores de la ácido grasa sintasa y se pueden emplear, inter alia, para el tratamiento de enfermedades tales como cáncer, enfermedades cardiovasculares, lesión del sistema nervioso central y diferentes formas de inflamación. Reivindicación 1: Compuestos de la fórmula (1) en donde R denota Ar o Het; Y denota -CO-W o -N(R⁴)CO-W¹; W denota NR²R², Het¹, CH₂Het¹, A, Cyc, Ar o CH₂Ar, -CONR²R² o Het¹; W¹ denota NR²R², Het¹, CH₂Het¹, A, Cyc, Ar, CH₂Ar, CH₂Cyc o CH(OH)CH₂OH; R¹ denota H, F, Cl, Br, OH, CN, NO₂, A, OA, SA, SO₂Me, COA, CONH₂, CONHA o CONA₂; R², R² denotan cada uno, de modo independiente entre si, H, A o [C(R³)₂]ₙCyc; X¹, X², X³ denotan cada uno, de modo independiente entre sí, CR⁸ o N; X⁴ denota CR⁸ o N; X⁵ denota CR⁸ o N; R⁴ denota H o A; A denota alquilo no ramificado o ramificado con 1 - 10 átomos de C, en donde dos átomos de carbono adyacentes pueden formar un enlace doble y/o uno o dos grupos CH y/o CH₂ no adyacentes pueden estar reemplazados por átomos de N, O y/o S y en donde 1 - 7 átomos de H pueden estar reemplazados por R⁵; Cyc denota cicloalquilo con 3 - 7 átomos de C, que no está sustituido o que está monosustituido con OH, Hal o A; A denota alquilo no ramificado o ramificado con 1 - 6 átomos de C, en donde 1 - 5 átomos de H pueden estar reemplazados por F; R⁵ denota F, Cl u OH; Ar denota fenilo, que no está sustituido o que está mono-, di-, tri-, tetra- o pentasustituido con Hal, A, O[C(R³)₂]ₙHet¹, Ar¹, [C(R³)₂]ₚOR³, [C(R³)₂]ₚN(R³)₂, NO₂, CN, [C(R³)₂]ₚCOOR³, CON(R³)₂, Het¹, OCH₂Cyc, [C(R³)₂]ₚN(R³)₂, N(R³)₂COA, NR³SO₂A, [C(R³)₂]ₚSO₂N(R³)₂, S(O)ₙA, O[C(R³)₂]ₘN(R³)₂, NHCOOA, NHCON(R³)₂ y/o COA; Ar¹ denota fenilo o naftilo, que no está sustituido o que está mono-, di-, tri-, tetra- o pentasustituido con Hal, A, [C(R³)₂]ₚOR³, [C(R³)₂]ₚN(R³)₂, NO₂, CN, [C(R³)₂]ₚCOOR³, [C(R³)₂]ₚN(R³)₂, N(R³)₂COA, NR³SO₂A, [C(R³)₂]ₚSO₂N(R³)₂, S(O)ₙA, O[C(R³)₂]ₘN(R³)₂, NHCOOA, NHCON(R³)₂ y/o COA; R³ denota H o alquilo no ramificado o ramificado con 1 - 6 átomos de C; R⁸ denota H o A; Het denota un heterociclo saturado, insaturado o aromático mono- o bicíclico que tiene 1 a 4 átomos de N, O y/o S, que no está sustituido o que está mono-, di-, tri-, tetra- o pentasustituido con Hal, A, O[C(R³)₂]ₙOA, [C(R³)₂]ₙN(R³)₂, SR³, NO₂, CN, COOR³, CON(R³)₂, COHet¹, NR³COA, NR³SO₂A, SO₂N(R³)₂, S(O)ₙA, O[C(R³)₂]ₘN(R³)₂, NHCOOA, NHCON(R³)₂, CHO, COA, =S, =NH, =NA Y/U =O (oxígeno del carbonilo); Het¹ denota un heterociclo saturado, insaturado o aromático mono- o bicíclico que tiene 1 a 4 átomos de N, O y/o S, que no está sustituido o que está mono-, di-, tri-, tetra- o pentasustituido con Hal, A, [C(R³)₂]ₙOR³, [C(R³)₂]ₙN(R³)₂, SR³, NO₂, CN, COOR³, CON(R³)₂, NR³COA, NR³SO₂A, SO₂N(R³)₂, S(O)ₙA, O[C(R³)₂]ₘN(R³)₂, NHCOOA, NHCON(R³)₂, CHO, COA, =S, =NH, =NA Y/U =O (oxígeno del carbonilo); Hal denota F, Cl, Br o I; m denota 1, 2 ó 3; n denota 0, 1 ó 2; p denota 0, 1, 2, 3 ó 4;q denota 0, 1, 2 ó 3; y sus sales, tautómeros, estereoisómeros farmacéuticamente aceptables, incluyendo sus mezclas en todas las proporciones.
ARP140102798A 2013-07-29 2014-07-28 Derivados 1,3-disustituidos de ciclopentano AR097086A1 (es)

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