发明名称 Pyrrolo[2,3-B]pyridine CDK9 kinase inhibitors
摘要 Disclosed are compounds of Formula (IIIa),; wherein R1, R2, R3, X1, X2, X3, X4, X5, have any of the values defined therefore in the specification, and pharmaceutically acceptable salts thereof. The compounds may be used as agents in the treatment of diseases, including cancer. Also provided are pharmaceutical compositions comprising one or more compounds of Formula (IIIa).
申请公布号 US9073922(B2) 申请公布日期 2015.07.07
申请号 US201414207886 申请日期 2014.03.13
申请人 AbbVie, Inc. 发明人 Gong Jianchun;Tao Zhi-Fu;Penning Thomas D.;Souers Andrew J.;Tong Yunsong;Zhu Guidong
分类号 C07D401/10;A61K31/437;A61K31/4353;C07D471/04;A61K31/497;A61K31/5377 主分类号 C07D401/10
代理机构 代理人 Sun Chanqxia
主权项 1. A compound of formula (IIIa), or a pharmaceutically acceptable salt thereof,wherein X1, and X4 are N; and the remaining are CR3A; R1 is selected from the group consisting of cycloalkyl, cycloalkenyl, heterocycloalkyl, and heterocycloalkenyl; wherein the R1 cycloalkyl, cycloalkenyl, heterocycloalkyl and heterocycloalkenyl are optionally substituted with one or more substituents independently selected from the group consisting of R5, OR5, SR5, S(O)R5, SO2R5, C(O)R5, CO(O)R5, OC(O)R5, OC(O)OR5, NH2, NHR5, N(R5)2, NHC(O)R5, NR5C(O)R5, SO2NHC(O)R5, SO2NR5C(O)R5, NHS(O)2R5, NR5S(O)2R5, NHC(O)OR5, NR5C(O)OR5, SO2NHC(O)OR5, SO2NR5C(O)OR5, NHSO2NHC(O)OR5, NHSO2NR5C(O)OR5, NR5SO2NR5C(O)OR5, NR5SO2NHC(O)OR5, NHC(O)NH2, NHC(O)NHR5, NHC(O)N(R5)2, NR5C(O)NHR5, NR5C(O)N(R5)2, OC(O)NH2, OC(O)NHR5, OC(O)N(R5)2, OC(O)NHSO2R5, OC(O)NR5SO2R5, C(O)NH2, C(O)NHR5, C(O)N(R5)2, C(O)NHOH, C(O)NHOR5, C(O)NHSO2R5, C(O)NR5SO2R5, SO2NH2, SO2NHR5, SO2N(R5)2, OSO2NH2, OSO2NHR5, OSO2N(R5)2, C(O)NHCN, C(O)NR5CN, S(O)(N)R5, S(O)(N)R5SO2R5, C(O)H, C(O)OH, (O), OH, CN, NO2, F, Cl, Br and I; R2 is selected from the group consisting of hydrogen, C1-C4 alkyl, NO2, CN, C(O)NH2, C(O)OR2A, F, Cl, Br, and I; R2A is selected from the group consisting of C1-C6 alkyl, C2-C6 alkenyl, and C2-C6 alkynyl; R3A, at each occurrence, is each independently selected from the group consisting of H, R6, OR6, SR6, S(O)R6, C(O)R6, CO(O)R6, OC(O)R6, OC(O)OR6, NH2, NHR6, N(R6)2, NHC(O)R6, NR6C(O)R6, NHS(O)2R6, NR6S(O)2R6, NHC(O)OR6, NR6C(O)OR6, NHC(O)NH2, NHC(O)NHR6, NHC(O)N(R6)2, NR6C(O)NHR6, NR6C(O)N(R6)2, C(O)NH2, C(O)NHR6, C(O)N(R6)2, C(O)NHOH, C(O)NHOR6, C(O)NHSO2R6, C(O)NR6SO2R6, C(O)H, C(O)OH, (O), OH, CN, NO2, F, Cl, Br and I; R4 is selected from the group consisting of R4A, OR4A, C(O)NH2, CN, F, Cl, Br, and I; R4A is selected from the group consisting of hydrogen, C1-C6 alkyl, C2-C6 alkenyl, and C2-C6 alkynyl; R5, at each occurrence, is independently selected from the group consisting of C1-C8 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, aryl, heteroaryl, heterocycloalkyl, heterocycloalkenyl, cycloalkyl, and cycloalkenyl; wherein each R5 C1-C8 alkyl, C2-C6 alkenyl, and C2-C6 alkynyl is optionally substituted with one or more substituents independently selected from the group consisting of R7, OR7, SR7, S(O)R7, SO2R7, C(O)R7, CO(O)R7, OC(O)R7, OC(O)OR7, NH2, NHR7, N(R7)2, NHC(O)R7, NR7C(O)R7, NHS(O)2R7, NR7S(O)2R7, NHC(O)OR7, NR7C(O)OR7, NHC(O)NH2, NHC(O)NHR7, NHC(O)N(R7)2, NR7C(O)NHR7, NR7C(O)N(R7)2, C(O)NH2, C(O)NHR7, C(O)N(R7)2, C(O)NHOH, C(O)NHOR7, C(O)NHSO2R7, C(O)NR7SO2R7, SO2NH2, SO2NHR7, SO2N(R7)2, B(OH)2, C(O)H, C(O)OH, OH, CN, NO2, F, Cl, Br and I; wherein each R5 aryl, cycloalkyl, cycloalkenyl, heteroaryl, heterocycloalkyl, and heterocycloalkenyl is optionally substituted with one or more substituents independently selected from the group consisting of R8, OR8, SR8, S(O)R8, SO2R8, C(O)R8, CO(O)R8, OC(O)R8, OC(O)OR8, NH2, NHR8, N(R8)2, NHC(O)R8, NR8C(O)R8, NHS(O)2R8, NR8S(O)2R8, NHC(O)OR8, NR8C(O)OR8, NHC(O)NH2, NHC(O)NHR8, NHC(O)N(R8)2, NR8C(O)NHR8, NR8C(O)N(R8)2, C(O)NH2, C(O)NHR8, C(O)N(R8)2, C(O)NHOH, C(O)NHOR8, C(O)NHSO2R8, C(O)NR8SO2R8, SO2NH2, SO2NHR8, SO2N(R8)2, C(O)H, C(O)OH, (O), OH, CN, NO2, F, Cl, Br and I; R6, at each occurrence, is independently selected from the group consisting of C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, phenyl, heteroaryl, heterocycloalkyl, heterocycloalkenyl, cycloalkyl, and cycloalkenyl; wherein each R6C1-C6 alkyl, C2-C6 alkenyl, and C2-C6 alkynyl is optionally substituted with one or more substituents independently selected from the group consisting of R9, OR9, SR9, S(O)R9, SO2R9, C(O)R9, CO(O)R9, OC(O)R9, OC(O)OR9, NH2, NHR9, N(R9)2, NHC(O)R9, NR9C(O)R9, NHS(O)2R9, NR9S(O)2R9, NHC(O)OR9, NR9C(O)OR9, NHC(O)NH2, NHC(O)NHR9, NHC(O)N(R9)2, NR9C(O)NHR9, NR9C(O)N(R9)2, C(O)NH2, C(O)NHR9, C(O)N(R9)2, C(O)NHOH, C(O)NHOR9, C(O)NHSO2R9, C(O)NR9SO2R9, SO2NH2, SO2NHR9, SO2N(R9)2, C(O)H, C(O)OH, OH, CN, NO2, F, CI, Br and I; wherein each R6 phenyl, cycloalkyl, cycloalkenyl, heteroaryl, heterocycloalkyl, and heterocycloalkenyl is optionally substituted with one or more substituents independently selected from the group consisting of R10, OR10, SR10, S(O)R10, SO2R10, C(O)R10, CO(O)R10, OC(O)R10, OC(O)OR10, NH2, NHR10, N(R10)2, NHC(O)R10, NR10C(O)R10, NHS(O)2R10, NR10S(O)2R10, NHC(O)OR10, NR10C(O)OR10, NHC(O)NH2, NHC(O)NHR10, NHC(O)N(R10)2, NR10C(O)NHR10, NR10C(O)N(R10)2, C(O)NH2, C(O)NHR10, C(O)N(R10)2, C(O)NHOH, C(O)NHOR10, C(O)NHSO2R10, C(O)NR10SO2R10, SO2NH2, SO2NHR10, SO2N(R10)2, C(O)H, C(O)OH, (O), OH, CN, NO2, F, CI, Br and I; R7, at each occurrence, is independently selected from the group consisting of C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, aryl, heteroaryl, heterocycloalkyl, heterocycloalkenyl, cycloalkyl, and cycloalkenyl; wherein each R7 C1-C6 alkyl, C2-C6 alkenyl, and C2-C6 alkynyl is optionally substituted with one or more substituents independently selected from the group consisting of R13, OR13, NH2, NHR13, N(R13)2, C(O)H, C(O)OH, OH, CN, NO2, F, CI, Br and I; wherein each R7 aryl, cycloalkyl, cycloalkenyl, heteroaryl, heterocycloalkyl, and heterocycloalkenyl is optionally substituted with one or more substituents independently selected from the group consisting of R11, OR11, SR11, S(O)R11, SO2R11, C(O)R11, CO(O)R11, OC(O)R11, OC(O)OR11, NH2, NHR11, N(R11)2, NHC(O)R11, NR11C(O)R11, NHS(O)2R11, NR11S(O)2R11, NHC(O)OR11, NR11C(O)OR11, NHC(O)NH2, NHC(O)NHR11, NHC(O)N(R11)2, NR11C(O)NHR11, NR11C(O)N(R11)2, C(O)NH2, C(O)NHR11, C(O)N(R11)2, C(O)NHOH, C(O)NHOR11, C(O)NHSO2R11, C(O)NR11SO2R11, SO2NH2, SO2NHR11, SO2N(R11)2, C(O)H, C(O)OH, (O), OH, CN, NO2, F, CI, Br and I; R8, at each occurrence, is independently selected from the group consisting of C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, and heterocycloalkyl; wherein each R8 C1-C6 alkyl, C2-C6 alkenyl, and C2-C6 alkynyl is optionally substituted with one or more substituents independently selected from the group consisting of aryl, heteroaryl, SO2R8A, C(O)OR8A, C(O)NH2, C(O)NHR8A, C(O)N(R8A)2, C(O)NHSO2R8A, C(O)NR8ASO2R8A, NH2, C(O)H, C(O)OH, OH, CN, NO2, F, CI, Br and I; wherein each R8 heterocycloalkyl is optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, NO2, F, CI, Br and I; R8A, at each occurrence, is independently selected from the group consisting of C1-C6 alkyl, C2-C6 alkenyl, and C2-C6 alkynyl; R9, at each occurrence, is independently selected from the group consisting of C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, aryl, heteroaryl, heterocycloalkyl, heterocycloalkenyl, cycloalkyl, and cycloalkenyl; wherein each R9 aryl, cycloalkyl, cycloalkenyl, heteroaryl, heterocycloalkyl, and heterocycloalkenyl is optionally substituted with one or more substituents independently selected from the group consisting of R12, OR12, SR12, S(O)R12, SO2R12, C(O)R12, CO(O)R12, OC(O)R12, OC(O)OR12, NH2, NHR12, N(R12)2, NHC(O)R12, NR12C(O)R12, NHS(O)2R12, NR12S(O)2R12, NHC(O)OR12, NR12C(O)OR12, NHC(O)NH2, NHC(O)NHR12, NHC(O)N(R12)2, NR12C(O)NHR12, NR12C(O)N(R12)2, C(O)NH2, C(O)NHR12, C(O)N(R12)2, C(O)NHOH, C(O)NHOR12, C(O)NHSO2R12, C(O)NR12SO2R12, SO2NH2, SO2NHR12, SO2N(R12)2, C(O)H, C(O)OH, (O), OH, CN, NO2, F, CI, Br and I; R10, at each occurrence, is independently selected from the group consisting of C1-C6 alkyl, C2-C6 alkenyl, and C2-C6 alkynyl; wherein each R10 C1-C6 alkyl, C2-C6 alkenyl, and C2-C6 alkynyl is optionally substituted with one or more substituents independently selected from the group consisting of NH2, C(O)H, C(O)OH, OH, CN, NO2, F, CI, Br and I; R11, at each occurrence, is independently selected from the group consisting of C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, aryl, and heteroaryl; wherein each R11 C1-C6 alkyl, C2-C6 alkenyl, and C2-C6 alkynyl is optionally substituted with one or more substituents independently selected from the group consisting of OR11A, NH2, NHR11A, N(R11A)2, C(O)H, C(O)OH, OH, CN, NO2, F, CI, Br and I; wherein each R11 aryl and heteroaryl is optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl, C1-C6 haloalkyl, NH2, C(O)H, C(O)OH, OH, CN, NO2, F, CI, Br and I; R11A, at each occurrence, is independently selected from the group consisting of C1-C6 alkyl, C2-C6 alkenyl, and C2-C6 alkynyl; R12, at each occurrence, is independently selected from the group consisting of C1-C6 alkyl, C2-C6 alkenyl, and C2-C6 alkynyl; wherein each R12 C1-C6 alkyl, C2-C6 alkenyl, and C2-C6 alkynyl is optionally substituted with one or more substituents independently selected from the group consisting of NH2, NHR14, N(R14)2, C(O)H, C(O)OH, OH, CN, NO2, F, CI, Br and I; R13, at each occurrence, is independently selected from the group consisting of C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, aryl, heteroaryl, cycloalkyl, cycloalkenyl, and heterocycloalkyl, heterocycloalkenyl; wherein each R13 C1-C6 alkyl, C2-C6 alkenyl, and C2-C6 alkynyl is optionally substituted with one or more substituents independently selected from the group consisting of R15, OR15, C(O)H, C(O)OH, OH, CN, NO2, F, CI, Br and I; wherein each R13 aryl, cycloalkyl, cycloalkenyl, heteroaryl, heterocycloalkyl, and heterocycloalkenyl is optionally substituted with one or more substituents independently selected from the group consisting of R16, OR16, C(O)H, C(O)OH, (O), OH, CN, NO2, F, CI, Br and I; R14, at each occurrence, is independently selected from the group consisting of C1-C6 haloalkyl, C1-C6 alkyl, C2-C6 alkenyl, and C2-C6 alkynyl; R15, at each occurrence, is independently selected from the group consisting of C1-C6 haloalkyl, C1-C6 alkyl, C2-C6 alkenyl, and C2-C6 alkynyl; wherein each R15 C1-C6 alkyl, C2-C6 alkenyl, and C2-C6 alkynyl is optionally substituted with one or more OCH3; and R16, at each occurrence, is independently selected from the group consisting of C1-C6 haloalkyl, C1-C6 alkyl, C2-C6 alkenyl, and C2-C6 alkynyl.
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