AR063151A1 - Inhibidores de metaloproteasas de matriz - Google Patents

Inhibidores de metaloproteasas de matriz

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Publication number
AR063151A1
AR063151A1 ARP070104423A ARP070104423A AR063151A1 AR 063151 A1 AR063151 A1 AR 063151A1 AR P070104423 A ARP070104423 A AR P070104423A AR P070104423 A ARP070104423 A AR P070104423A AR 063151 A1 AR063151 A1 AR 063151A1
Authority
AR
Argentina
Prior art keywords
alkyl
phenyl
heteroaryl
group
indolyl
Prior art date
Application number
ARP070104423A
Other languages
English (en)
Original Assignee
Janssen Pharmaceutica Nv
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Publication date
Application filed by Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of AR063151A1 publication Critical patent/AR063151A1/es

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    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/14Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D295/145Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
    • C07D295/15Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
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    • A61P9/00Drugs for disorders of the cardiovascular system
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    • C07D211/14Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom
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Abstract

Además, la presente se refiere a métodos que tratan trastornos relacionados con las metaloproteasas de matriz. Más particularmente, los compuestos de la presente son utiles para tratar el accidente cerebrovascular. Reivindicacion 1: Compuestos de la formula (1) en donde: R1 es H, -CH3, R2 es H, -CH3, R3 es H, alquilo C1-3, fenilo, heteroarilo de 5 o 6 miembros; en donde dicho fenilo y dicho heteroarilo de 5 o 6 miembros están opcionalmente sustituidos con uno o dos sustituyentes seleccionados del grupo que consiste de Cl, F, -N(alquilo C1-4)2, -NO2, -CN, -OCF3, -CF3, -Oalquilo C1-4, y alquilo C1-4; R4 es formulas (2) en donde: A=B es -CH=CH- o S; X es O, S, ?-C:::C-?-, -CH=CH- (cis o trans), o un enlace directo; Y es CH o N; Z es S o O o NH; Ra es uno o dos sustituyentes independientemente seleccionados del grupo que consiste de H, CI, F, -OH, -NH2, -N(alquilo C1-4)2, -NO2, -CN, -CO2H, -CONH2, -OCF3, -CF3, -Oalquilo C1-4, y alquilo C1-4; R5 es alquilo C1-4, fenilo, - alquil C1-3-fenilo, -alquil C1-3-heteroarilo, -N(alquilo C1-4)2, formulas (3) en donde dicho fenilo, -alquil C1-3-fenilo, y -alquil C1-3-heteroarilo están opcionalmente sustituidos con uno o dos sustituyentes seleccionados del grupo que consiste de CI, F, -N(alquilo C1-4)2, -NO2, -CN, -CONH2, -OCF3, -CF3, -Oalquilo C1-4, y alquilo C1-4; y Rb es -alquilo C1-4, -SO2aIquilo C1-4, -COalquilo C1-4 o -CO2CH2- fenilo; R6 es H, alquilo C1-4, alilo, -alquilo C2-4-O-aIquilo C1-4, -alquil C1-3-fenilo, - alquil C1-3-heteroarilo, - alquil C2-4-N(alquilo C1-4)2, formulas (4) en donde dicho -alquil C1-3-fenilo y dicho -alquil C1-3-heteroarilo están opcionalmente sustituidos con uno o dos sustituyentes seleccionados del grupo que consiste de CI, F, - N(alquilo C1-4)2, -NO2, -CN, -CONH2, -OCF3, -CF3, -Oalquilo C1-4, y alquilo C1-4, en donde Rc es -alquilo C1-4, -SO2alquilo C1-4, -COalquilo C1-4, CO2CH2-fenilo; R7 es -OR8, -SR8, -NR9R10, o -NR11COR12 en donde R8 es H, alquilo C1-4, fenilo, heteroarilo, indolilo, alquil C1-2-fenilo, alquil C1-2-indolilo, o alquil C1-2-heteroarilo; en donde dicho fenilo, heteroarilo, indolilo, alquil C1-2-fenilo, alquil C1-2-indolilo, y alquil C1-2-heteroarilo están opcionalmente sustituidos con uno o dos sustituyentes seleccionados del grupo que consiste de CI, F, -N(alquilo C1-4)2, -NO2, -CN. -CONH2, -OCF3, -CF3, -Oalquil C1-4, y alquil C1-4; R9 es H, alquilo C1-4, fenilo, heteroarilo, heteroarilo benzofusionado, naftalenilo, cicloalquilo C3- 7, heterociclilo de 5-7 miembros, éster bencílico del ácido alquil C2-4-carbámico, -alquil C2-4-1,5,5trimetil-imidazolidin-2,4-diona, alquil C1-3-fenilo, alquil C1-3-heteroarilo, alquil C1-3-heteroarilo benzofusionado, y en donde dicho alquil C1-3- fenilo, alquil C1-3-heteroarilo, alquil C1-3-heteroarilo benzofusionado, fenilo, heteroarilo, y dicho heteroarilo benzofusionado están opcionalmente sustituidos con uno o dos sustituyentes seleccionados del grupo que consiste de CI, F, -N(alquilo C1- 4)2, -NO2, -CN, -CONH2, -OCF3,.-CF3, - Oalquilo C1-4, y alquilo C1-4; R10 es H, o alquilo C1-4; alternativamente, R9 y R10 pueden juntarse con el nitrogeno unido para formar un anillo seleccionado del grupo que consiste de formulas (5) en donde dicho anillo está opcionalmente sustituido con uno o dos sustituyentes seleccionados del grupo que consiste de: -CH2OaIquilo C1-2, -N(alquilo C1-4)2, -Oalquilo C1-4, alquilo C1-4, -OH, -SO2alquilo C1-4, -COalquilo C1-4, -CONHalquilo C1-4, fenilo, fluorofenilo, clorofenilo, bromofenilo, y -CO2CH2fenilo, R11 es H, o alquilo C1-4; R12 es alquilo C1-4, indolilo, fenilo, heteroarilo, cicloalquilo C3-7, morfolinilo, piperidinilo, piperazinilo, N-metil piperazinilo, tetrahidropiranilo, pirrolidinilo, alquil C1-2-fenilo, alquil C1-2-indolilo o alquil C1-2-heteroarilo; en donde dicho indolilo, fenilo, heteroarilo, alquil C1-2-fenilo, alquil C1-2-indolilo o alquil C1-2-heteroarilo están opcionalmente sustituidos con uno o dos sustituyentes seleccionados del grupo que consiste de CI, F, -N(alquilo C1-4)2, -NO2, -CN, -CONH2, -OCF3, -CF3, -Oalquilo C1-4 y alquilo C1-4; y solvatos, hidratos, tautomeros y sales farmacéuticamente aceptables de los mismos.
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