AR070522A1 - Derivados de pirido 4,3-d-pirimidinona como inhibidores de cinasa, una composicion farmaceutica y un metodo para el tratamient0 de una enfermedad, un medicamento en base al compuesto y el uso de este para la fabricacion de un medicamento - Google Patents
Derivados de pirido 4,3-d-pirimidinona como inhibidores de cinasa, una composicion farmaceutica y un metodo para el tratamient0 de una enfermedad, un medicamento en base al compuesto y el uso de este para la fabricacion de un medicamentoInfo
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- AR070522A1 AR070522A1 ARP090100303A ARP090100303A AR070522A1 AR 070522 A1 AR070522 A1 AR 070522A1 AR P090100303 A ARP090100303 A AR P090100303A AR P090100303 A ARP090100303 A AR P090100303A AR 070522 A1 AR070522 A1 AR 070522A1
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- Prior art keywords
- carbon atoms
- alkyl
- halogen
- heterocycloalkyl
- substituted
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- 150000001875 compounds Chemical class 0.000 title abstract 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract 2
- 201000010099 disease Diseases 0.000 title 1
- 229940043355 kinase inhibitor Drugs 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 229940126601 medicinal product Drugs 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 121
- 125000000217 alkyl group Chemical group 0.000 abstract 31
- 229910052736 halogen Inorganic materials 0.000 abstract 28
- 150000002367 halogens Chemical class 0.000 abstract 27
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 21
- 125000003545 alkoxy group Chemical group 0.000 abstract 19
- 125000003118 aryl group Chemical group 0.000 abstract 15
- 125000001072 heteroaryl group Chemical group 0.000 abstract 14
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 13
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 8
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 8
- 125000001424 substituent group Chemical group 0.000 abstract 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 5
- 125000004429 atom Chemical group 0.000 abstract 5
- 229910052799 carbon Inorganic materials 0.000 abstract 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 3
- 125000004001 thioalkyl group Chemical group 0.000 abstract 3
- 125000000732 arylene group Chemical group 0.000 abstract 2
- 125000005549 heteroarylene group Chemical group 0.000 abstract 2
- 125000006588 heterocycloalkylene group Chemical group 0.000 abstract 2
- -1 - (CH2) nR9 Inorganic materials 0.000 abstract 1
- 208000024172 Cardiovascular disease Diseases 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 206010003246 arthritis Diseases 0.000 abstract 1
- 208000015114 central nervous system disease Diseases 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 208000030159 metabolic disease Diseases 0.000 abstract 1
- 230000002062 proliferating effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
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- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- A61P17/00—Drugs for dermatological disorders
- A61P17/04—Antipruritics
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- A61P17/00—Drugs for dermatological disorders
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Los compuestos divulgados son utiles en los trastornos del SNC, en el tratamiento de las enfermedades inflamatorias como artritis, trastornos metabolicos (diabetes), enfermedades cardiovasculares y trastornos proliferativos. Reivindicacion 1: Un compuesto de la formula (1), una sal farmacéuticamente aceptable, o un solvato farmacéuticamente aceptable del mismo en donde R1 es -NR6R7, (CH2)nR19, L3R19, R20, arilo de 6 a 14 átomos de carbono, cicloalquilo de 3 a 8 átomos de carbono, heterocicloalquilo de 2 a 14 átomos de carbono, o heteroarilo de 3 a 13 átomos de carbono, en donde el arilo de 6 a 14 átomos de carbono, cicloalquilo de 3 a 8 átomos de carbono, heterocicloalquilo de 2 a 14 átomos de carbono, y heteroarilo de 3 a 13 átomos de carbono de R1 está opcionalmente sustituido con 1 a 3 sustituyentes seleccionados independientemente a partir de halogeno, nitro, ciano, alquilo de 1 a 6 átomos de carbono, alcoxilo de 1 a 6 átomos de carbono, tioalquilo de 1 a 6 átomos de carbono, hidroxialquilo de 1 a 6 átomos de carbono, alquilo de 1 a 6 átomos de carbono sustituido por halogeno, alcoxilo de 1 a 6 átomos de carbono sustituido por halogeno, cicloalquilo de 3 a 12 átomos de carbono, heterocicloalquilo de 2 a 14 átomos de carbono, arilo de 6 a 14 átomos de carbono, heteroarilo de 3 a 13 átomos de carbono, -X2S(O)0-2R17, -X2S(O)0-2X2R19, -X2NR17R17, -X2NR17C(O)R17, -X2C(O)NR17R17, -X2NR17C(O)R19, -X2C(O)NR17R19, -X2C(O)R19, -X2NR17X2R19 y -X2OX2R19 en donde X2 es un enlace o alquileno de 1 a 4 átomos de carbono; L3 es un enlace, alquilo de 1 a 6 átomos de carbono, o alcoxilo de 1 a 6 átomos de carbono; en donde los grupos alquilo de 1 a 6 átomos de carbono, y alcoxilo de 1 a 6 átomos de carbono de L3 están opcionalmente sustituidos con 1 a 3 sustituyentes seleccionados independientemente a partir de halogeno, -CN, -alquilo de 1 a 6 átomos de carbono, alcoxilo de 1 a 6 átomos de carbono, -OR13, -C(O)R13, -OC(O)R13, -C(O)OR13, -N(R12)2, -C(O)N(R12)2, -N(R12)C(O)R13, -N(R12)C(O)OR13, heterocicloalquilo de 2 a 14 átomos de carbono, -S(O)2R13, -S(O)2N(R12)2, R13, -(C(R12)2)nR13, -(C(R12)2)nR14, alquilo de 1 a 6 átomos de carbono sustituido por halogeno, y alcoxilo de 1 a 6 átomos de carbono sustituido por halogeno; R17 es H o alquilo de 1 a 6 átomos de carbono; y R19 es R20, cicloalquilo de 3 a 12 átomos de carbono, heterocicloalquilo de 2 a 14 átomos de carbono, arilo de 6 a 14 átomos de carbono, o heteroarilo de 3 a 13 átomos de carbono, en donde el arilo de 6 a 14 átomos de carbono, heteroarilo de 3 a 13 átomos de carbono, cicloalquilo de 3 a 12 átomos de carbono, y heterocicloalquilo de 2 a 14 átomos de carbono, de R19, están opcionalmente sustituidos con 1 a 3 radicales seleccionados independientemente a partir de halogeno, nitro, ciano, alquilo de 1 a 6 átomos de carbono, alcoxilo de 1 a 6 átomos de carbono, tioalquilo de 1 a 6 átomos de carbono, hidroxi-alquilo de 1 a 6 átomos de carbono, alquilo de 1 a 6 átomos de carbono sustituido por halogeno, y alcoxilo de 1 a 6 átomos de carbono sustituido por halogeno; R2 y R3 se seleccionan independientemente a partir de H, (CH2)nR11, -C(O)R12, -CR12=NOCR12,-NR8R10, halogeno, R20, alquilo de 1 a 6 átomos de carbono, alquenilo de 2 a 6 átomos de carbono, alquinilo de 2 a 6 átomos de carbono, alcoxilo de 1 a 6 átomos de carbono, tioalquilo de 1 a 6 átomos de carbono, hidroxi-alquilo de 1 a 6 átomos de carbono, alquilo de 1 a 6 átomos de carbono sustituido por halogeno, y alcoxilo de 1 a 6 átomos de carbono sustituido por halogeno, arilo de 6 a 14 átomos de carbono, heteroarilo de 3 a 13 átomos de carbono, y heterocicloalquilo de 2 a 14 átomos de carbono, en donde el arilo de 6 a 14 átomos de carbono, y heterocicloalquilo de 2 a 14 átomos de carbono, de R2 y R3, están opcionalmente sustituidos con 1 a 3 sustituyentes seleccionados independientemente a partir de halogeno, -CN, -NO2, -OR12, -OR10, =O, -C(O)R12, -OC(O)R12, -C(O)OR12, -N(R11)2, -N(R12)2, -N(R12R10), -N(R12R11), -NR12C(O)N(R12)2, -NHS(O)2R13, -(CR12R12)nR11, -SR8, -C(O)N(R12R10), -N(R12)C(O)R13, -C(O)N(R11)2, -C(O)N(R12)2, -(CR12R12)nR11, -(CH2)nR12, -(CH2)nR13, -O(CH2)nR13, -(CH2)nR14, -O(CH2)nR14, -(CH2)nR16, -S(O)2R12, -S(O)2N(R11)2, -S(O)2N(R12)2, R12, R10, -OR13, -C(O)R13, OC(O)R13, -C(O)OR13, -S(O)2R13, -R13, heterocicloalquilo de 2 a 14 átomos de carbono, alquilo de 1 a 6 átomos de carbono, alcoxilo de 1 a 6 átomos de carbono, hidroxi-alquilo de 1 a 6 átomos de carbono, alquilo de 1 a 6 átomos de carbono sustituido por halogeno, y alcoxilo de 1 a 6 átomos de carbono sustituido por halogeno; R4 es H, alquilo de 1 a 6 átomos de carbono, o -(CR12R12)nR11; R5 es H o alquilo de 1 a 6 átomos de carbono; R6 es H, arilo de 6 a 14 átomos de carbono, heteroarilo de 3 a 13 átomos de carbono, heterocicloalquilo de 2 a 14 átomos de carbono, alquilo de 1 a 6 átomos de carbono, cicloalquilo de 3 a 8 átomos de carbono, alquilo de 1 a 6 átomos de carbono sustituido por halogeno, -(CH2)nR9, R20, -L3R9 o -Y1-L1-R14, en donde Y1 es arileno, heteroarileno, o heterocicloalquileno, y L1- es un enlace, -O-, -C(O)-, -C(O)N(R11)-, -(C(R12)2)n- u -O(CH2)n-; y en donde el arilo de 6 a 14 átomos de carbono, heteroarilo de 3 a 13 átomos de carbono, alquilo de 1 a 6 átomos de carbono, alquilo de 1 a 6 átomos de carbono sustituido por halogeno, heterocicloalquilo de 2 a 14 átomos de carbono, y cicloalquilo de 3 a 8 átomos de carbono de R6 e Y1 están opcionalmente sustituidos con 1 a 3 sustituyentes seleccionados independientemente a partir de halogeno, -CN, -OR12, -OR10, -C(O)R12, -OC(O)R12, -C(O)OR12, -N(R11)2, -N(R12)2, -N(R12R10), -N(R12R11), -(CR12R12)nR11, -SR8, -NR12C(O)N(R12)2, -C(O)N(R12R10) -N(R12)C(O)R13, -C(O)N(R11)2, -C(O)N(R12)2, -(CR12R12)nR11, -(CH2)nR12, -(CH2)nR13, -O(CH2)nR13, -(CH2)nR14, -O(CH2)nR14, -(CH2)nR16, -S(O)2R12, -S(O)2N(R11)2, -S(O)2N(R12)2, R12, R10, -OR13, -C(O)R13, OC(O)R13, -C(O)OR13, -S(O)2R13, -R13, heterocicloalquilo de 2 a 14 átomos de carbono, alquilo de 1 a 6 átomos de carbono, alcoxilo de 1 a 6 átomos de carbono, hidroxi-alquilo de 1 a 6 átomos de carbono, alquilo de 1 a 6 átomos de carbono sustituido por halogeno, alcoxilo de 1 a 6 átomos de carbono sustituido por halogeno; R7 es H o alquilo de 1 a 6 átomos de carbono; R8 es H o alquilo de 1 a 6 átomos de carbono; R9 es R20, arilo de 6 a 14 átomos de carbono, heteroarilo de 3 a 13 átomos de carbono, heterocicloalquilo de 2 a 14 átomos de carbono, alquilo de 1 a 6 átomos de carbono, cicloalquilo de 3 a 8 átomos de carbono, o Y2-L2-R14, en donde Y2 es un enlace, arileno, heteroarileno, o heterocicloalquileno, y L2- es un enlace, -O-, u -O(CH2)n-; y en donde el arilo de 6 a 14 átomos de carbono, heteroarilo de 3 a 13 átomos de carbono, cicloalquilo de 3 a 8 átomos de carbono, y heterocicloalquilo de 2 a 14 átomos de carbono, de R9 e Y2, están opcionalmente sustituidos con 1 a 3 sustituyentes seleccionados independientemente a partir de halogeno, halogeno, -CN, =O, -OR12, -OR10, -C(O)R12, -OC(O)R12, -C(O)OR12, -N(R11)2, -N(R12)2, -N(R12R10), -N(R12R11), -(CR12R12)nR11, -SR8, -NR12C(O)N(R12)2, -C(O)N(R12R10), -N(R12)C(O)R13, -C(O)N(R11)2, -C(O)N(R12)2, -(CR12R12)nR11, -(CH2)nR12, -(CH2)nR13, -O(CH2)nR13, -(CH2)nR14, -O(CH2)nR14, -(CH2)nR16, -S(O)2R12, -S(O)2N(R11)2, -S(O)2N(R12)2, R12, R10, -OR13, -C(O)R13, -OC(O)R13, -C(O)OR13, -S(O)2R13, -R13, heterocicloalquilo de 2 a 14 átomos de carbono, alquilo de 1 a 6 átomos de carbono, alcoxilo de 1 a 6 átomos de carbono, hidroxi-alquilo de 1 a 6 átomos de carbono, alquilo de 1 a 6 átomos de carbono sustituido por halogeno, o alcoxilo de 1 a 6 átomos de carbono sustituido por halogeno; R10 es alquilo de 1 a 6 átomos de carbono sustituido por halogeno, arilo de 6 a 14 átomos de carbono, heteroarilo de 3 a 13 átomos de carbono, heterocicloalquilo de 2 a 14 átomos de carbono, cicloalquilo de 3 a 8 átomos de carbono o -(CH2)nR11, en donde el arilo de 6 a 14 átomos de carbono, heteroarilo de 3 a 13 átomos de carbono, heterocicloalquilo de 2 a 14 átomos de carbono, y cicloalquilo de 3 a 8 átomos de carbono de R10 están opcionalmente sustituidos con 1 a 3 sustituyentes seleccionados independientemente a partir de halogeno, -CN, hidroxilo, -OR12, -OR10, -C(O)R12, -OC(O)R12, -C(O)OR12, -N(R11)2, -N(R12)2, -N(R12R10), -N(R12R11), -(CR12R12)nR11, -SR8, -NR12C(O)N(R12)2, -C(O)N(R12R10), -N(R12)C(O)R13, -C(O)N(R11)2, -C(O)N(R12)2, -(CR12R12)nR11, -(CH2)nR12, -(CH2)nR13, -O(CH2)nR13, -(CH2)nR14, -O(CH2)nR14, -(CH2)nR16, -S(O)2R12, .-S(O)2N(R11)2, -S(O)2N(R12)2, R12, R10, -OR13, -C(O)R13, OC(O)R13, -C(O)OR13, -S(O)2R13, -R13, heterocicloalquilo de 2 a 14 átomos de carbono, alquilo de 1 a 6 átomos de carbono, alcoxilo de 1 a 6 átomos de carbono, hidroxi-alquilo de 1 a 6 átomos de carbono; alquilo de 1 a 6 átomos de carbono sustituido por halogeno, o alcoxilo de 1 a 6 átomos de carbono sustituido por halogeno; R11 es -N(R12)2, -OR13, R20, -C(O)N(R12)2, -S(O)2R13, -S(O)2N(R12)2, arilo de 6 a 14 átomos de carbono, heteroarilo de 3 a 13 átomos de carbono, alquilo de 1 a 6 átomos de carbono, cicloalquilo de 3 a 8 átomos de carbono, o heterocicloalquilo de 2 a 14 átomos de carbono, en donde el arilo de 6 a 14 átomos de carbono, heteroarilo de 3 a 13 átomos de carbono, alquilo de 1 a 6 átomos de carbono, cicloalquilo de 3 a 8 átomos de carbono, y heterocicloalquilo de 2 a 14 átomos de carbono, de R11, están opcionalmente sustituidos con 1 a 3 sustituyentes seleccionados independientemente a partir de halogeno, -CN, -OR12, -OR10, -C(O)R12, -OC(O)R12, -C(O)OR12, -N(R11)2, -N(R12)2, -N(R12R10), -N(R12R11), -(CR12R12)nR11, -SR8, -NR12C(O)N(R12)2, -C(O)N(R12R10), -N(R12)C(O)R13, -C(O)N(R11)2, -C(O)N(R12)2, -(CR12R12)nR11, -(CH2)nR12, -(CH2)nR13, -O(CH2)nR13, (CH2)nR14, -O(CH2)nR14, (CH2)nR16, -S(O)2R12, -S(O)2N(R11)2, S(O)2N(R12)2, R12, R10, -OR13, -C(O)R13, OC(O)R13, -C(O)OR13, -S(O)2R13, -R13, heterocicloalquilo de 2 a 14 átomos de carbono, alquilo de 1 a 6 átomos de carbono, alcoxilo de 1 a 6 átomos de carbono, hidroxialquilo de 1
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- 2009-01-27 KR KR1020107019403A patent/KR20100118989A/ko not_active Abandoned
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