AR053710A1 - Compuestos espiroheterociclicos y sus usos como agentes terapeuticos - Google Patents
Compuestos espiroheterociclicos y sus usos como agentes terapeuticosInfo
- Publication number
- AR053710A1 AR053710A1 ARP060101419A ARP060101419A AR053710A1 AR 053710 A1 AR053710 A1 AR 053710A1 AR P060101419 A ARP060101419 A AR P060101419A AR P060101419 A ARP060101419 A AR P060101419A AR 053710 A1 AR053710 A1 AR 053710A1
- Authority
- AR
- Argentina
- Prior art keywords
- heteroaryl
- aryl
- heterocyclyl
- aralkyl
- alkyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 239000003814 drug Substances 0.000 title 1
- 229940124597 therapeutic agent Drugs 0.000 title 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 21
- 125000003118 aryl group Chemical group 0.000 abstract 19
- 125000000623 heterocyclic group Chemical group 0.000 abstract 19
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 18
- 125000000217 alkyl group Chemical group 0.000 abstract 15
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 14
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 11
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 10
- 125000001188 haloalkyl group Chemical group 0.000 abstract 10
- 125000004415 heterocyclylalkyl group Chemical group 0.000 abstract 10
- 229910052739 hydrogen Inorganic materials 0.000 abstract 10
- 239000001257 hydrogen Substances 0.000 abstract 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 9
- 125000005843 halogen group Chemical group 0.000 abstract 7
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 7
- 125000003342 alkenyl group Chemical group 0.000 abstract 5
- 125000000304 alkynyl group Chemical group 0.000 abstract 5
- -1 halalkyl Chemical group 0.000 abstract 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 5
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 3
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- 125000004450 alkenylene group Chemical group 0.000 abstract 2
- 125000002947 alkylene group Chemical group 0.000 abstract 2
- 125000004419 alkynylene group Chemical group 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 108010052164 Sodium Channels Proteins 0.000 abstract 1
- 102000018674 Sodium Channels Human genes 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 230000006806 disease prevention Effects 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
Classifications
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- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/22—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains four or more hetero rings
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
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Abstract
La presente son utiles para el tratamiento y/o prevencion, de enfermedades o condiciones mediadas por los canales de sodio, tales como el dolor. Composiciones farmacéuticas que comprenden los compuestos y métodos para preparar y usar los compuestos. Reivindicacion 1: Un compuesto de formula (1), donde: p es entre 1 y 4; j y k son cada uno en forma independiente 0, 1 , 2 o 3; Q es - C(R1a)H-, -C(O)-, -O-, -S-, -N(R5)-, -CF2-, -C(O)O-, -C(O)N(R5)- o -N(R5)C(O)-; R1a es hidrogeno o - OR5; la formula (2) es un anillo heteroarilo fusionado o un anillo heterociclilo fusionado; R1 es hidrogeno, alquilo, alquenilo, alquinilo, halalquilo, arilo, cicloalquilo, cicloalquilalquilo, heteroarilo, heterociclilo, -R8-OR5, -R8-CN, -R9- P(O)(OR5)2, o -R9-O-R9-OR5; o R1 es aralquilo sustiutido con -C(O) N(R6)R7 donde: R6 es hidrogeno, alquilo, arilo o aralquilo; y R7 es hidrogeno, alquilo, haloalquilo, -R9-CN, -R9-OR5, -R9-N(R4)R5, arilo, aralquilo, cicloalquilo, cicloalquilalquilo, heterociclilo, heterociclilalquilo, heteroarilo, heteroarilalquilo; o R6 y R7, junto con el nitrogeno al cual están unidos, forman un heterociclilo o heteroarilo; y donde cada grupo arilo, aralquilo, cicloalquilo, cicloalquilalquilo, heterociclilo, heterociclilalquilo, heteroarilo y heteroarilo para R6 y R7 puede estar opcionalmente sustituido con uno o más sustituyentes seleccionados entre el grupo que consiste en alquilo, cicloalquilo, arilo, aralquilo, halo, haloalquilo, -R8-CN, -R8-OR5, heterociclilo y heteroarilo; o R1 es aralquilo opcionalmente sustituido con -R8-OR5, -C(O)OR5, halo, haloalquilo, alquilo, nitro, ciano, arilo (opcionalmente sustituido con ciano), aralquilo (opcionalmente sustituido con uno o más grupos alquilo), heterociclilo o heteroarilo; o R1 es -R9-N(R10)R11, -R9-N(R12)C(O)R11 o -R9-N(R10)C(O)N(R10)R11 donde: cada R10 es hidrogeno, alquilo, arilo o aralquilo; cada R11 es hidrogeno, alquilo, haloalquilo, cicloalquilo, cicloalquilalquilo, arilo, aralquilo, heterociclilo, heterociclilalquilo, heteroarilo, heteroarilalquilo, -R9-OC(O)R5, -R9-C(O)OR5, -R9-C(O)N(R4)R5, -R9-C(O)R5, -R9-OR5, o -R9-CN; R12 es hidrogeno, alquilo, arilo, aralquilo o -C(O)R5; y donde cada grupo arilo, aralquilo, cicloalquilo, cicloalquilalquilo, heterociclilo, heterociclilalquilo, heteroarilo y heteroarilalquilo para R10 y R11 puede estar opcionalmente sustituido con uno o más sustituyentes seleccionados entre el grupo que consiste en alquilo, cicloalquilo, arilo, aralquilo, halo, haloalquilo, nitro, -R8-CN, -R8-OR5, -R8-C(O)R5, heterociclilo y heteroarilo; o R1 es heterociclilalquilo o heteroarilalquilo donde el grupo heterociclilalquilo o heteroarilo está opcionalmente sustituido con uno o más sustituyentes seleccionados entre el grupo que consiste en alquilo, halo, haloalquilo, -R8-OR5, -R8-C(O)OR5, arilo y aralquilo; cada R2 se selecciona en forma independiente entre el grupo que consiste en hidrogeno, alquilo, alquenilo, alquinilo, alcoxi, halo, haloalquilo, haloalquenilo, haloalcoxi, cicloalquilo, cicloalquilalquilo, arilo, aralquilo, aralquenilo, heterociclilo, heterociclilalquilo, heteroarilo, heteroarilalquilo, -R8-CN, -R8-NO2, -R8-OR5, -R8-N(R4)R5, -N=C(R4)R5, -S(O)mR4, - R8-C(O)R4; -C(S)R4, -C(R4)2C(O)R5, -R8-C(O) OR4, -C(S)OR4, -R8-C(O)N(R4)R5, -C(S)N(R4)R5, -N(R5)C(O)R4, -N(R5)C(S)R4, -N(R5)C(O)OR4, -N(R5)C(S)OR4, -N(R5)C(O)N(R4)R5, - N(R5)C(S)N(R4)R5, -N(R5)S(O)nR4, -N(R5)S(O)nN(R4)R5, -R8-S(O)nN(R4)R5, - N(R5)C(=NR5)N(R4)R5, y -N(R5)C(=N-CN)N(R4)R5, donde cada m es en forma independiente 0, 1, o 2 y cada n es en forma independiente 1 o 2; y donde cada uno de los grupos cicloalquilo, cicloalquilalquilo, arilo, aralquilo, aralquenilo, heterociclilo, heterociclilalquilo, heteroarilo y heteroarilalquilo para cada R2 puede estar opcionalmente sustituido con uno o más sustituyentes seleccionados entre el grupo que consiste en alquilo, alquenilo, alquinilo, alcoxi, halo, haloalquilo, haloalquenilo, haloalcoxi, cicloalquilo, cicloalquilalquilo, arilo, aralquilo, aralquenilo, heterociclilo, heterociclilalquilo, heteroarilo, heteroarilalquilo, -R8-CN, -R8-NO2, -R8-OR5, -R8-N(R4)R5, -S(O)mR4, -R8-C(O)R4; -R8-C(O)OR4, -R8- C(O)N(R4)R5, -N(R5)C(O)R4, y -N(R5)S(O)nR4, donde cada m es en forma independiente 0, 1 o 2 y cada n es en forma independiente 1 o 2; o dos grupos R2 adyacentes, junto con el anillo heteroarilo fusionado o el anillo heterociclilo fusionado al cual están directamente unidos, pueden formar un anillo fusionado seleccionado entre cicloalquilo, arilo, heterociclilo y heteroarilo, y los grupos R2 restantes, de estar presentes, son como se ha descrito; R3a, R3b, R3c y R3d se seleccionan en forma independiente entre sí entre el grupo que consiste en hidrogeno, alquilo, alquenilo, alquinilo, alcoxi, halo, haloalquilo, haloalquenilo, haloalcoxi, cicloalquilo, cicloalquilalquilo, arilo, aralquilo, aralquenilo, heterociclilo, heterociclilalquilo, heteroarilo, heteroarilalquilo, -R8-CN, -R8-NO2, -R8-OR5, -R8-N(R4)R5, -N=C(R4) R5, -S(O)mR4, -R8-C(O)R4; -C(S)R4, -C(R4)2C(O)R5, -R8-C(O)OR4, -C(S)OR4, -R8-C(O)N(R4)R5, -C(S)N(R4)R5, -N(R5)C(O)R4, -N(R5) C(S)R4, -N(R5)C(O)OR4, -N(R5)C(S)OR4, -N(R5)C(O)N(R4)R5, - N(R5)C(S)N(R4)R5, -N(R5)S(O)nR4, -N(R5)S(O)nN(R4)R5, -R8-S(O) nN(R4)R5, -N(R5)C(=NR5)N(R4)R5, y -N(R5)C(N=C(R4)R5)N(R4)R5, donde cada m es en forma independiente 0, 1 o 2 y cada n es en forma independiente 1 o 2; o R3a y R3b, o R3b y R3c, o R3c y R3d, junto con los átomos de carbono del anillo a los que están directamente unidos, pueden formar un anillo fusionado seleccionado entre cicloalquilo, heterociclilo, arilo o heteroarilo, y los grupos R3a, R3b, R3c o R3d restantes son como se ha definido; cada R4 y R5 se selecciona en forma independiente entre el grupo que consiste en hidrogeno, alquilo, alquenilo, alquinilo, haloalquilo, alcoxialquilo, cicloalquilo, cicloalquilalquilo, arilo, aralquilo, heterociclilo, y heteroarilo; o cuando R4 y R5 están ambos unidos al mismo átomo de nitrogeno, entonces; R4 y R5, junto con el átomo de nitrogeno al cual están unidos, pueden formar un heterociclilo o heteroarilo; y cada R8 es un enlace directo o una cadena alquileno lineal o ramificada, una cadena alquenileno lineal o ramificada o una cadena alquinileno lineal o ramificada; y cada R9 es una cadena alquileno lineal o ramificada, una cadena alquenileno lineal o ramificada o una cadena alquinileno lineal o ramificada; como estereoisomeros, enantiomeros, tautomeros del mismo o mezclas de los mismos; o solvatos, prodrogas o sales aceptables para uso farmacéutico del mismo.
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