AR046337A1 - Imidazopirazina inhibidoras de las tirosinquinasas - Google Patents
Imidazopirazina inhibidoras de las tirosinquinasasInfo
- Publication number
- AR046337A1 AR046337A1 ARP040103731A ARP040103731A AR046337A1 AR 046337 A1 AR046337 A1 AR 046337A1 AR P040103731 A ARP040103731 A AR P040103731A AR P040103731 A ARP040103731 A AR P040103731A AR 046337 A1 AR046337 A1 AR 046337A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkynyl
- alkenyl
- cycloalkenyl
- nr222r333
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 17
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 12
- 125000000217 alkyl group Chemical group 0.000 abstract 11
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 8
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 7
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 6
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 6
- 125000001424 substituent group Chemical group 0.000 abstract 6
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 abstract 5
- 125000003342 alkenyl group Chemical group 0.000 abstract 4
- 125000004414 alkyl thio group Chemical group 0.000 abstract 4
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 4
- 125000001475 halogen functional group Chemical group 0.000 abstract 4
- 125000005018 aryl alkenyl group Chemical group 0.000 abstract 3
- 125000005015 aryl alkynyl group Chemical group 0.000 abstract 3
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 125000004043 oxo group Chemical group O=* 0.000 abstract 3
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 2
- 101100516568 Caenorhabditis elegans nhr-7 gene Proteins 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000004449 heterocyclylalkenyl group Chemical group 0.000 abstract 2
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 102000004190 Enzymes Human genes 0.000 abstract 1
- 108090000790 Enzymes Proteins 0.000 abstract 1
- 108091008648 NR7C Proteins 0.000 abstract 1
- 102000004022 Protein-Tyrosine Kinases Human genes 0.000 abstract 1
- 108090000412 Protein-Tyrosine Kinases Proteins 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 150000001602 bicycloalkyls Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 125000004475 heteroaralkyl group Chemical group 0.000 abstract 1
- 125000004366 heterocycloalkenyl group Chemical group 0.000 abstract 1
- 125000004415 heterocyclylalkyl group Chemical group 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 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
- 125000005541 phosphonamide group Chemical group 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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Abstract
Inhiben la enzima IGF-1R y son útiles para el tratamiento y/o la prevención de diferentes enfermedades y afecciones que responden al tratamiento por inhibición de tirosinquinasas. Reivindicación 1: Un compuesto representado por la fórmula (1), o una sal del mismo aceptable para uso farmacéutico, en la cual Q1 es arilo1, heteroarilo1, cicloalquilo, heterociclilo, cicloalquenilo, o heterocicloalquenilo, cualquiera de los cuales está substituido opcionalmente con entre uno y cinco substituyentes G1 independientes; R1 es alquilo, cicloalquilo, bicicloalquilo, arilo, heteroarilo, aralquilo, heteroaralquilo, heterociclilo, o heterobicicloalquilo, cualquiera de los cuales está substituido opcionalmente con uno o más substituyentes G11 independientes; G1 y G41 son independientemente halo, oxo, -CF3, -OCF3, -OR2, -NR2R3(R3a)j1, -C(O)R2, -CO2R, -CONRaR3, -NO2, -CN, -S(O)j1R2, -SO2NR2R3, NR2(C=O)R3, NR2(C=O)OR3, NR2(C=O)NR2R3, NR2S(O)j1R3, -(C=S)OR2, -(C=O)SR2, - NR2(C=NR3)NR2aR3a, -NR2(C=NR3)OR2a, -NR2(C=NR3)SR3a, -O(C=O)OR2, -O(C=O)NR2R3, -O(C=O)SR2, -S(C=O)OR2, -S(C=O)NR2R3, alquilo C0-10, alquenilo C2-10, alquinilo C2-10, alcoxi C1-10alquilo C1-10, alcoxi C1-10alquenilo C2-10, alcoxi C1-10alquinilo C2- 10, alquiltio C1-10alquilo C1-10, alquiltio C1-10alquenilo C2-10, alquiltio C1-10alquinilo C2-10, cicloalquilo C3-8, cicloalquenilo C3-8, cicloalquil C3-8alquilo C1-10, cicloalquenil C3-8alquilo C1-10, cicloalquil C3-8alquenilo C1-10, cicloalquenil C3-8alquenilo C2-10, cicloalquil C3-8alquinilo C2-10, cicloalquenil C3-8alquinilo C2-10, heterociclil-alquilo C0-10,heterociclil-alquenilo C2-10, o heterociclil-alquinilo C2-10, cualquiera de los cuales está substituido opcionalmente con uno o más substituyentes independientes halo, oxo, -CF3, -OCF3, -OR222, -NR222R333(R333a)j1a, -C(O)R222, -CO2R222, -CONR222R333, -NO2, -CN, -S(O)j1aR222, -SO2NR222R333, NR222(C=O)R333, NR222(C=O)OR333, NR222(C=O)NR222R333, NR222S(O)j1aR333, -(C=S)OR222, - (C=O)R222, -NR222(C=NR333)NR222aR333a, -NR222(C=NR333)OR222a, -NR222(C=NR333)SR333a, -O(C=O)OR222, -O(C=O)NR222R333, -O(C=O)SR222, -S(C=O)OR222, o -S(C=O)NR222R333; o -(X1)n-(Y1)m-R4; o aril-alquilo C0-10, aril-alquenilo C2-10, o aril-alquinilo C2- 10, cualquiera de los cuales está substituido opcionalmente con uno o más substituyentes independientes, -CF3, -OCF3, -OR222, -NR222R333(R333a)j2a, -C(O)R222, -CO2R222, -CONR222R333, -NO2, -CN, -S(O)j2aR222, -SO2NR222R333, NR222(C=O)R333, NR222(C=O)OR333, NR222(C=O)NR222R333, NR222S(O)j2aR333, -(C=S)OR222, -(C=O)SR222, -NR222(C=NR333)NR222aR333a, -NR222(C=NR333)OR222a, -NR222(C=NR333)SR333a, -O(C=O)OR222, -O(C=O)NR222R333, -O(C=O)SR222, -S(C=O)OR222, o -S(C=O)NR222R333; o hetaril- alquilo C0-10, hetaril-alquenilo C2-10, o hetaril-alquinilo C2-10, cualquiera de los cuales está substituido opcionalmente con uno o más substituyentes independientes halo, -CF3, -OCF3, -OR222, -NR222R333(R333a)j3a, -C(O)R222, -CO2R222, - CONR222R333, -NO2, -CN, -S(O)j3aR222, -SO2NR222R333, NR222(C=O)R333, NR222(C=O)OR333, NR222(C=O)NR222R333, NR222S(O)j3aR333, -(C=S)OR222, -(C=O)SR222, -NR222(C=NR333)NR222aR333a, -NR222(C=NR333)OR222a, -NR222(C=NR333)SR333a, -O(C=O)OR222, - O(C=O)NR222R333, -O(C=O)SR222, -S(C=O)OR222, o -S(C=O)NR222R333; G11 es halo, oxo, -CF3, -OCF3, -OR21, -NR21R31(R3a1)j4, -C(O)R21, -CO2R21, -CONR21R31, -NO2, -CN, -S(O)j4R21, -SO2NR21R31, NR21(C=O)R31, NR21(C=O)OR31, NR21(C=O)NR21R31, NR21S(O)j4R31, -(C=S)OR21, -(C=O)SR21, -NR21(C=NR31)NR2a1R3a1, -NR21(C=NR31)OR2a1, -NR21(C=NR31)SR3a1, -O(C=O)OR21, -O(C=O)NR21R31, -O(C=O)SR21, -S(C=O)OR21, -S(C=O)NR21R31, -P(O)OR21OR31, alquilo C0-10, alquenilo C2-10, alquinilo C2-10, alcoxi C1-10alquilo C1-10, alcoxi C1-10alquenilo C2-10, alcoxi C1-10alquinilo C2-10, alquiltio C1-10alquilo C1-10, alquiltio C1-10alquenilo C2-10, alquiltio C1-10alquinilo C2-10, cicloalquilo C3-8, cicloalquenilo C3-8, cicloalquil C3-8alquilo C1-10, cicloalquenil C3-8alquilo C1-10, cicloalquil C3-8alquenilo C2-10, cicloalquenil C3-8alquenilo C2-10, cicloalquil C3-8alquinilo C2-10, cicloalquenil C3-8alquinilo C2-10, heterociclil-alquilo C0-10, heterociclil-alquenilo C2-10, o heterociclil-alquinilo C2-10, cualquiera de los cuales está substituido opcionalmente con uno o más substituyentes independientes halo, oxo, -CF3, -OCF3, -OR2221, -NR2221R3331(R333a1)j4a, -C(O)R2221, -CO2R2221, -CONR2221R3331, -NO2, -CN, -S(O)j4aR2221, -SO2NR2221R3331, NR2221(C=O)R3331, NR2221(C=O)OR3331, NR2221(C=O)NR2221R3331, NR2221S(O)j4aR3331, -(C=S)OR2221, -(C=O)SR2221, -NR2221(C=NR3331)NR222a1R333a1, -NR2221(C=NR3331)OR222a1, -NR2221(C=NR3331)SR333a1, -O(C=O)OR2221, -O(C=O)NR2221R3331, -O(C=O)SR2221, -S(C=O)OR2221, - P(O)OR2221OR3331, o -S(C=O)NR2221R3331; o aril-alquilo C0-10, aril-alquenilo C2-10, o aril-alquinilo C2-10, cualquiera de los cuales está substituido opcionalmente con uno o más substituyentes independientes halo, -CF3, -OCF3, -OR2221, - NR2221R3331(R333a1)j5a, -C(O)R2221, -CO2R2221, -CONR2221R3331, -NO2, -CN, -S(O)j5aR2221, -SO2NR2221R3331, NR2221(C=O)R3331, NR2221(C=O)OR3331, NR2221(C=O)NR2221R3331, NR2221S(O)j5aR3331, -(C=S)OR2221, -(C=O)SR2221, -NR2221(C=NR3331)NR222a1R333a1, - NR2221(C=NR3331)OR222a1, -NR2221(C=NR3331)SR333a1, -O(C=O)OR2221, -O(C=O)NR2221R3331, -O(C=O)SR2221, -S(C=O)OR2221, -P(O)OR2221OR3331, o -S(C=O)NR2221R3331; o hetaril-alquilo C0-10, hetaril-alquenilo C2-10, o hetaril-alquinilo C2-10, cualquiera de los cuales está substituido opcionalmente con uno o más independientes halo, -CF3, -OCF3, -OR2221, -NR2221R3331(R333a1)j6a, -C(O)R2221, -CO2R2221, -CONR2221R3331, -NO2, -CN, -S(O)j6aR2221, -SO2NR2221R3331, NR2221(C=O)R3331, NR2221(C=O)OR3331, NR2221(C=O)NR2221R3331, NR2221S(O)j6aR3331, -(C=S)OR2221, -(C=O)SR2221, -NR2221(C=NR3331)NR222a1R333a1, -NR2221(C=NR3331)OR222a1, -NR2221(C=NR3331)SR333a1, -O(C=O)OR2221, -O(C=O)NR2221R3331, -O(C=O)SR2221, -S(C=O)OR2221, -P(O)OR2221OR3331, o - S(C=O)NR2221R3331; o G11 se toma junto con el carbono al cual está unido para formar una unión doble que está substituida con R5 y G111; R2, R2a, R3, R3a, R222, R222a, R333, R333a, R21, R2a1, R31, R3a1, R2221, R222a1, R3331, y R333a1 son cada uno independientemente igual a alquilo C0-10, alquenilo C2-10, alquinilo C2-10, alcoxi C1-10alquilo C1-10, alcoxi C1-10alquenilo C2-10, alcoxi C1-10alquinilo C2-10, alquiltio C1-10alquilo C1-10, alquiltio C1-10alquenilo C2-10, alquiltio C1-10alquinilo C2-10, cicloalquilo C3-8, cicloalquenilo C3-8, cicloalquil C3-8alquilo C1-10, cicloalquenil C3-8alquilo C1-10, cicloalquil C3-8alquenilo C2-10, cicloalquenil C3-8alquenilo C2-10, cicloalquil C3-8alquinilo C2-10, cicloalquenil C3-8alquinilo C2-10, heterociclil-alquilo C0-10, heterociclil-alquenilo C2-10, o heterociclil-alquinilo C2-10, cualquiera de los cuales está opcionalmente substituido con uno o más substituyentes G111; o aril-alquilo C0-10, aril-alquenilo C2-10, o aril-alquinilo C2-10, hetaril-alquilo C0-10, hetaril-alquenilo C2-10, o hetaril-alquinilo C2-10, cada uno de los cuales está substituido opcionalmente con uno o más substituyentes G111; o en el caso de -NR2R3(R3a)j1 o -NR222R333(R333a)j1a o -NR222R333(R333a)j2a o - NR2221R3331(R333a1)j3a o -NR2221R3331(R333a1)j4a o -NR2221R3331(R333a1)j5a o -NR2221R3331(R333a1)j6a, R2 y R3 o R222 y R333 o R2221 y R3331 tomados junto con el nitrógeno al cual están unidos forman un anillo de 3-10 miembros cíclico saturado, cíclico no saturado, cíclico saturado heterocíclico, o cíclico no saturado heterocíclico, en donde dicho anillo está opcionalmente substituido con uno o más substituyentes G111; X1 e Y1 son, cada uno independientemente -O-, -NR7-, -S(O)J7-, -CR5R6-, -N(C(O)OR7)-, -N(C(O)R7)-, -N(SO2R7)-, -CH2O-, -CH2S-, -CH2N(R7)-, -CH(NR7)-, -CH2N(C(O)R7)-, -CH2N(C(O)OR7)-, -CH2N(SO2R7)-, -CH(NHR7)-, -CH(NHC(O)R7)-, -CH(NHSO2R7)-, -CH(NHC(O)OR7)-, -CH(OC(O)R7)-, -CH(OC(O)NHR7)-, -CH=CH-, -CsC-, -C(=NOR7)-, - C(O)-, -CH(OR7)-, -C(O)N(R7)-, -N(R7)C(O)-, -N(R7)S(O)-, -N(R7)S(O)2-, -OC(O)N(R7)-, -N(R7)C(O)N(R7)-, -NR7C(O)O-, -S(O)N(R7)-, -S(O)2N(R7)-, -N(C(O)R7)S(O)-, -N(C(O)R7)S(O)2-, -N(R7)S(O)N(R7)-, -N(R7)S(O)2N(R7)-, -C(O)N(R7)C(O)-, -S(O)N(R7)C(O)-, - S(O)2N(R7)C(O)-, -OS(O)N(R7)-, -OS(O)2N(R7)-, -N(R7)S(O)O-, -N(R7)S(O)2O-, -N(R7)S(O)C(O), -N(R7)S(O)2C(O)-, -SON(C(O)R7)-, -SO2N(C(O)R7)-, -N(R7)SON(R7)-, -N(R7)SO2N(R7)-, -C(O)O-, -N(R7)P(OR8)O-, -N(R7)P(OR8)-, -N(R7)P(O)(OR8)O-, -N(R7)P(O)(OR8)- , -N(C(O)R7)P(OR8)O-, -N(C(O)R7)P(OR8)-, -N(C(O)R7)P(O)(OR8)O-, -N(C(O)R7)P(OR8)-, -CH(R7)S(O)-,-CH(R7)S(O)2-, -CH(R7)N(C(O)OR7)-, -CH(R7)N(C(O)R7)-, -CH(R7)N(SO2R7), -CH(R7)O-, -CH(R7)S-, -CH(R7)N(R7)-, -CH(R7)N(C(O)R7)-, -CH(R7)N(C(O)OR7)-, - CH(R7)N(SO2R7)-, -CH(R7)C(=NOR7)-, -CH(R7)C(O)-, -CH(R7)CH(OR7)-, -CH(R7)C(O)N(R7)-, -CH(R7)N(R7)C(O)-, -CH(R7)N(R7)S(O)-, -CH(R7)N(R7)S(O)2-, -CH(R7)OC(O)N(R7)-, -CH(R7)N(R7)C(O)N(R7)-, -CH(R7)NR7C(O)O-, -CH(R7)S(O)N(R7)-, -CH(R7)S(O)2N(R7)-, - CH(R7)N(C(O)R7)S(O)-, -CH(R7)N(C(O)R7)S(O)-, -CH(R7)N(R7)S(O)N(R7)-, -CH(R7)N(R7)S(O)2N(R7)-, -CH(R7)C(O)N(R7)C(O)-, -CH(R7)S(O)N(R7)C(O)-, -CH(R7)S(O)2N(R7)C(O)-, -CH(R7)OS(O)N(R7)-, -CH(R7)OS(O)2N(R7)-, -CH(R7)N(R7)S(O)O-, -CH(R7)N(R7)S(O)2O-, - CH(R7)N(R7)S(O)C(O)-, -CH(R7)N(R7)S(O)2C(O)-, -CH(R7)SON(C(O)R7)-, -CH(R7)SO2N(C(O)R7)-, -CH(R7)N(R7)SON(R7)-, -CH(R7)N(R7)SO2N(R7)-, -CH(R7)C(O)O-, -CH(R7)N(R7)P(OR8)O-, -CH(R7)N(R7)P(OR8)-, -CH(R7)N(R7)P(O)(OR8)O-, -CH(R7)N(R7)P(O)(OR8)-, - CH(R7)N(C(O)R7)P(OR8)O-, -CH(R7)N(C(O)R7)P(OR8)-, -CH(R7)N(C(O)R7)P(O)(OR8)O-, o -CH(R7)N(C(O)R7)P(OR8)-; o X1 y Y1 cada uno está representado por una de las fórmulas estructurales (2), (3), (4), (5), (6) ó (7); R10, tomado junto con la fosfinamida o fosfonamida, es un sistema anular arilo, heteroarilo o heterociclilo de 5, 6 o 7 miembros; R5, R6 y G111 son, cada uno independientemente alquilo C0-10, alquenilo C2-10, alquinilo C2-10, alcoxi C1-10alquilo C1-10, alcoxi C1-10alquenilo C2-10, alcoxi C1-10alquinilo C2-10, alquiltio C1-10alquilo C1-10, alquiltio C1-10alquenilo C2-10, alquiltio C1-10alquinilo C2-10, cicloalquilo C3-8, cicloalquenilo C3-8, cicloalq
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- 2004-10-14 AR ARP040103731A patent/AR046337A1/es not_active Application Discontinuation
- 2004-10-14 ES ES04795392T patent/ES2372694T3/es not_active Expired - Lifetime
- 2004-10-14 CN CN2004800372564A patent/CN1898240B/zh not_active Expired - Fee Related
- 2004-10-14 US US10/965,182 patent/US7459554B2/en active Active
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- 2004-10-14 AU AU2004282219A patent/AU2004282219C1/en not_active Ceased
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- 2004-10-14 KR KR1020067009419A patent/KR100872204B1/ko not_active Expired - Fee Related
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- 2004-10-14 TW TW093131193A patent/TW200530238A/zh unknown
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2006
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| BRPI0415395A (pt) | 2006-12-12 |
| UA83509C2 (en) | 2008-07-25 |
| ATE525377T1 (de) | 2011-10-15 |
| RU2006116503A (ru) | 2007-11-20 |
| JP4916883B2 (ja) | 2012-04-18 |
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| US20060084654A1 (en) | 2006-04-20 |
| KR100872204B1 (ko) | 2008-12-09 |
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| EP1675860A2 (en) | 2006-07-05 |
| SG132683A1 (en) | 2007-06-28 |
| CN1898240A (zh) | 2007-01-17 |
| EP1675860B1 (en) | 2011-09-21 |
| AU2004282219C1 (en) | 2009-12-17 |
| AU2004282219A1 (en) | 2005-04-28 |
| WO2005037836A2 (en) | 2005-04-28 |
| US20080227788A9 (en) | 2008-09-18 |
| JP2007509060A (ja) | 2007-04-12 |
| AP2006003620A0 (en) | 2006-06-30 |
| US20090181940A1 (en) | 2009-07-16 |
| NO20062136L (no) | 2006-06-26 |
| ES2372694T3 (es) | 2012-01-25 |
| CN1898240B (zh) | 2011-08-03 |
| RU2405784C2 (ru) | 2010-12-10 |
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