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AR036132A1 - Pirazinas, formulacion farmaceutica, uso de estos compuestos en la fabricacion de medicamentos, procesos para la preparacion de estos compuestos e intermediarios - Google Patents

Pirazinas, formulacion farmaceutica, uso de estos compuestos en la fabricacion de medicamentos, procesos para la preparacion de estos compuestos e intermediarios

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Publication number
AR036132A1
AR036132A1 ARP020102533A ARP020102533A AR036132A1 AR 036132 A1 AR036132 A1 AR 036132A1 AR P020102533 A ARP020102533 A AR P020102533A AR P020102533 A ARP020102533 A AR P020102533A AR 036132 A1 AR036132 A1 AR 036132A1
Authority
AR
Argentina
Prior art keywords
alkyl
nr6r7
nr1r2
alkynyl
cycloalkyl
Prior art date
Application number
ARP020102533A
Other languages
English (en)
Original Assignee
Astrazeneca Ab
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 Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of AR036132A1 publication Critical patent/AR036132A1/es

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    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/36Radicals substituted by singly-bound nitrogen atoms
    • C07D213/42Radicals substituted by singly-bound nitrogen atoms having hetero atoms attached to the substituent nitrogen atom
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Abstract

Pirazinas que tienen la fórmula (1) en donde: Z es CH o N; Y es CONR5, NR5CO, SO2NR5, NR5SO2, CH2NR5, NR5CH2, NR5CONR5, alquileno C1-6, CH2CO, COCH2, CH=CH, OCH2 o CH2O; X es CH o N; P es fenilo o un anillo heteroaromático de 5 o 6 miembros que contiene uno o más heteroátomos seleccionados entre N, O ó S, y dicho anillo fenilo o anillo heteroaromático de 5 o 6 miembros puede opcionalmente estar fusionado con un anillo de 5 o 6 miembros saturado, parcialmente saturado o insaturado que contiene uno o más átomo seleccionados entre C, N, O ó S; Q es fenilo o un anillo heteroaromático de 5 o 6 miembros que contiene uno o más heteroátomos seleccionados entre N, O ó S, de los cuales por lo menos un átomo se selecciona entre nitrógeno; R es CHO, fluormetoxi, difluormetoxi, trifluormetoxi, alquilo C0-6(SO2)NR1R2, O alquilo C0-6(SO2)NR1R2, O alquilo C1-6(SO)NR1R2, alquilo C1-6(SO)NR1R2, alquilo C0-6NR1(SO)R2, O alquilo C1-6NR1(SO)R2, alquilo C0-6NR1(SO2)NR1R2, O alquilo C1-6 NR1(SO2)R2, alquilo C0-6 (SO2) alquilo C1-6NR1R2, O alquilo C0-6(SO2)alquilo C1-6 NR1R2, alquilo C0-6(SO)alquilo C1-6 NR1R2, O alquilo C1-6 (SO) alquilo C1-6NR1R2, alquilo C0-6 S alquilo C1-6 NR1R2, O alquilo C1-6 S alquilo C1-6 NR1R2, O alquilo C1-6 O alquilo C1-6, alquilo C1-6 O alquilo C1-6 NR1R2, O alquilo C1-6 O alquilo C1-6 NR1R2, alquilo C0-6 CONR10R11, O alquilo C0-6 CONR1R2, O alquilo C1-6 NR1R2, alquilo C0-6NR10 (CO)R11, O alquilo C1-6 NR1(CO)R2, alquilo C0-6NR11(CO)R10, alquilo C0-6COR11, O alquilo C1-6 COR1, alquilo C0-6NR10R11, alquilo C0-6 O(CO)R11, O alquilo C1-6 O (CO)R1, alquilo C0-6 C(NR10)NR10R11, alquilo C0-6C(NR11)N(R10)2, O alquilo C0-6 C(NR1)NR1R2, alquilo C0-6NR10(CO)OR11, O alquilo C1-6NR1(CO)OR2, alquilo C0-6NR11(CO)OR10, O alquilo C1-6 CN, NR1OR2, alquilo C0-6 (CO)OR8, O alquilo C1-6(CO)OR1, NR1 (CO)NR1R2, NR1(CO)(CO)R2, NR1(CO)(CO)NR1R2, OR12, ó SO3R1; R1 y R2 se seleccionan de manera independiente entre hidrógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, (CO)OR8, alquilheterocicloalquilo C0-6, alquilo C1-6 NR6R7, alquilarilo C0-6 y alquilheteroarilo C0-6, en donde cualquier de alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, alquilheterocicloalquilo C0-6, alquilarilo C0-6, alquilheteroarilo C0-6 puede estar sustituido con uno o más A; R1 y R2 pueden formar juntos un anillo heterocíclico de 5, 6 o 7 miembros sustituido que contiene uno o más heteroátomos seleccionados entre N, O ó S, cuyo anillo heterocíclico puede estar opcionalmente sustituido con A; R3 y R4 se seleccionan de manera independiente entre halo, nitro, CHO, alquilo C0-6CN, O alquilo C1-6 CN, alquilo C0-6OR6, O alquilo C1-6 OR6, fluormetilo, difluormetilo, trifluormetilo, fluormetoxi, difluormetoxi, trifluormetoxi, alquilo C0-6 NR6R7, O alquilo C1-6 NR6R7, O alquilo C1-6 O alquilo C1-6 NR6R7, NR6OR7 alquilo C0-6 CO2R6, O alquilo C1-6 CO2R6, alquilo C0-6 CONR6R7, O alquilo C1-6 CONR6R7, O alquilo C1-6 NR6(CO)R7, alquilo C0-6 NR6(CO)R7, O(CO)NR6R7, NR6(CO)OR7, NR6(CO)NR6R7, O(CO)OR6, O(CO)R6, alquilo C0-6COR6, O alquilo C1-6 COR6, NR6(CO)(CO)R6, NR6(CO)(CO)NR6R7, SR6, alquilo C0-6 (SO2)NR6R7, O alquilo C1-6 NR6(SO2)R7, O alquilo C0-6 (SO2)NR6R7, alquilo C0-6 (SO)NR6R7, O alquilo C1-6 (SO)NR6R7, SO3R6, alquilo C0-6NR6(SO2)NR6R7, alquilo C0-6NR6(SO)R7, O alquilo C1-6 NR6(SO)R7, O alquilo C0-6 SO2R6, alquilo C0-6SO2R6, alquilo C0-6SOR6, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, alquilarilo C0-6 y alquilheteroarilo C0-6, en donde cualquiera de alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, alquilarilo C0-6 y alquilheteroarilo C0-6 puede estar opcionalmente sustituido con uno o más A; m es 0, 1, 2, 3 o 4; n es 0, 1, 2, 3 ó 4; R5 es hidrógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, alquilarilo C0-6 y alquilheteroarilo C0-6, alquilo C1-6 NR6R7 o alquilo C1-6 CONR6R7; R6 y R7 se seleccionan de manera independiente entre hidrógeno, alquilo C1-6, (CO)OR8, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, alquilarilo C0-6 y alquilheteroarilo C0-6 y alquilo C1-6 NR8R9; R6 y R7 pueden formar juntos un anillo heterocíclico de 5 o 6 miembros sustituido, que contiene uno o más heteroátomos seleccionados entre N, O ó S, cuyo anillo heterocíclico puede estar opcionalmente sustituido con A; R8 y R9 se seleccionan de manera independiente entre hidrógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, alquilarilo C0-6 y alquilheteroarilo C0-6; R8 y R9 pueden formar juntos un anillo heterocíclico de 5 o 6 miembros que contiene uno o más heteroátomos seleccionados entre N, O ó S, cuyo anillo heterocíclico puede estar opcionalmente sustituido con A, R10 es hidrógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, alquilarilo C0-6 y alquilheteroarilo C0-6 o alquilo C1-6 NR8R9; R11 es alquilo C1-6 NR8R9 o alquilheterocicloalquilo C0-6; R10 y R11 pueden formar juntos un anillo heterocíclico de 5, 6 o 7 miembros que contiene uno o más heteroátomos seleccionados entre N, O ó S, cuyo anillo heterocíclico puede estar opcionalmente sustituido con A; R12 es un anillo heterocíclico de 5, 6 o 7 miembros que contiene uno o más heteroátomos seleccionados entre N, O ó S, cuyo anillo heterocíclico puede estar opcionalmente sustituido con A; en donde cualquiera de alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, alquilheterocicloalquilo C0-6, alquilarilo C0-6, alquilheteroarilo C0-6 definidos en R5 a R12 pueden estar sustituidos con uno o más A; A es halo, nitro, CHO, CN, OR6, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, fluormetilo, difluormetilo, trifluormetilo, fluormetoxi, difluormetoxi, trifluormetoxi, alquilo C0-6NR6R7, O alquilo C1-6, NR6R7, CO2R8, CONR6R7, NR6(CO)R6, O(CO)R6, COR6, SR6, (SO2)NR6R7, (SO)NR6R7, SO3R6, SO2R6 ó SOR6, como una base libre o como una sal farmacéuticamente aceptable de la misma, con la condición de que el compuesto no es 4[4-[5-amino-6-(fenilmetil)pirazinil]fenoxi]-etil éster del ácido butanoico; formulación farmacéutica, uso de estos compuestos en la fabricación de medicamentos procesos para la preparación de estos compuestos e intermediarios. Estos compuestos son útiles en terapia, especialmente en la prevención y/o el tratamiento de condiciones asociadas con glucógeno sintasa quinasa -3(GSK3).
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