Patent Application
20070135387
This invention pertains to compounds that inhibit protein kinases such as Aurora kinases, compositions containing the compounds and methods of treating diseases using the compounds.
Mitosis is a process by which a complete copy of a duplicated genome is segregated by the microtuble spindle apparatus into two daughter cells. Aurora kinases, key mitotic regulators required for genome stability, have been found to be overexpressed in human tumors. Given the central role of mitosis in the progression of maligncies, inhibitors of mitosis are expected to be useful for treating a broad range of tumors.
There is therefore an existing need in the therapeutic arts for inhibitors of Aurora kinases.
One embodiment of this invention, therefore, pertains to compounds that inhibit Aurora kinases, the compounds having formula (I)
A1 is C(O)NHR1, C(O)N(R1)2, NHC(O)R1, NR1C(O)R1, NHC(O)NHR1, NHC(O)N(R1)2, NR1C(O)NHR1, NR1C(O)N(R1)2, SO2NHR1, SO2N(R1)2, NHSO2R1, NR1SO2R1, OC(O)OR1, NHC(O)OR1, NR1C(O)OR1 or R5;
R1 is R2, R3, R4 or R5;
R2 is phenyl which is unfused or fused with benzene, heteroarene or R2A; R2A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R3 is heteroaryl which is unfused or fused with benzene, heteroarene or R3A; R3A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R4 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene, heteroarene or R4A; R4A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R5 is alkyl, alkenyl or alkynyl, each of which is substituted with one or two of independently selected R6, OR6, SR6, S(O)R6, SO2R6, NH2, NHR6, N(R6)2, C(O)R6, C(O)NH2, C(O)NHR6, C(O)N(R6)2, NHC(O)R6, NR6C(O)R6, NHSO2R6, NR6SO2R6, NHC(O)OR6, NR6C(O)OR6, SO2NH2, SO2NHR6, SO2N(R6)2, NHC(O)NH2, NHC(O)NHR6, NHC(O)N(R6)2, NR6C(O)N(R6)2, OH, (O), C(O)OH, CN, NH2, CF3, OCF3, CF2CF3, F, Cl, Br or I;
R6 is R7, R8 or R9;
R7 is phenyl which is unfused or fused with benzene, heteroarene or R7A; R7A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R8 is heteroaryl which is unfused or fused with benzene, heteroarene or R8A; R8A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R9 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene, heteroarene or R9A; R9A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
wherein the moieties represented by R1, R2, R3, R4, R5 and R6 are independently substituted with one or two of independently selected R10, OR10, SR10, S(O)R10, SO2R10, NH2, NHR10, N(R10)2, C(O)R10, C(O)OR10, C(O)NHR10, C(O)N(R10)2, NHC(O)R10, NR10C(O)R10,NHC(O)NHR10, NHC(O)N(R10)2, NR10C(O)NHR10, NR10C(O)N(R10)2, SO2NHR10, SO2N(R10)2, NHSO2R10, NR1SO2R10, OC(O)OR10, NHC(O)OR10 or NR1C(O)OR10;
R10 is R11, R12, R13 or R14;
R11 is phenyl which is unfused or fused with benzene, heteroarene or R11A; R11A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R12 is heteroaryl which is unfused or fused with benzene, heteroarene or R12A; R12A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R13 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene, heteroarene or R13A; R13A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R14 is alkyl, alkenyl or alkynyl, each of which is unsubstituted or substituted with one or two of independently selected R15 or NHC(O)NHR15;
R15 is R16, R17 R18;
R16 is phenyl which is unfused or fused with benzene, heteroarene or R16A; R16A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R17 is heteroaryl which is unfused or fused with benzene, heteroarene or R17A; R17A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R18 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl each of which is unfused or fused with benzene, heteroarene or R18A; R18A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
B1 is H, R19, C(O)NHR19, C(O)N(R19)2, NHC(O)R19, NR1C(O)R19, NHC(O)NHR19, NHC(O)N(R19)2, NR19C(O)NHR19, NR1C(O)N(R19)2, SO2NHR19, SO2N(R19)2, NHSO2R19, NR19SO2R19, OC(O)OR19, NHC(O)OR19, or NR19C(O)OR19;
R19 is R20, R21, R22 or R23;
R20 is phenyl which is unfused or fused with benzene, heteroarene or R20A; R20A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R21 is heteroaryl which is unfused or fused with benzene, heteroarene or R21A; R21A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R22 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene, heteroarene or R22A; R22A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R23 is alkyl, alkenyl or alkynyl, each of which is unsubstituted or substituted with one or two of independently selected R24, OR24, SR24, S(O)R24, SO2R24, NH2, NHR24, N(R24)2, C(O)R24, C(O)NH2, C(O)NHR24, C(O)N(R24)2, NHC(O)R24, NR24C(O)R24, NHSO24R24, NR24 SO2R24, NHC(O)OR24, NR24C(O)OR24, SO2NH2, SO2NHR24, SO2N(R24)2, NHC(O)NH2, NHC(O)NHR24, NHC(O)N(R24)2, NR24C(O)N(R24)2, OH, (O), C(O)OH, CN, NH2, CF3, OCF3, CF2CF3, F, Cl, Br or I;
R24 is R25, R26, R27, alkyl, alkenyl or alkynyl;
R25 is phenyl which is unfused or fused with benzene, heteroarene or R25A; R25A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R26 is heteroaryl which is unfused or fused with benzene, heteroarene or R26A; R26A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R27 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene, heteroarene or R27A; R27A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
C1 is O, S, S(O), SO2, NH, or N(C2);
C2 is R28, R29, R30 or R31;
R28 is phenyl which is unfused or fused with benzene, heteroarene or R28A; R28A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R29 is heteroaryl which is unfused or fused with benzene, heteroarene or R29A; R29A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R30 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene, heteroarene or R30A; R30A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R31 is alkyl, alkenyl or alkynyl, each of which is substituted with one or two of independently selected R32, OR32, SR32, S(O)R32, SO2R32, NH2, NHR32, N(R32)2, C(O)R32, C(O)NH2, C(O)NHR32, C(O)N(R32)2, NHC(O)R32, NR32C(O)R32, NHSO2R32, NR32SO2R32, NHC(O)OR32, NR32C(O)OR32, SO2NH2, SO2NHR32, SO2N(R32)2, NHC(O)NH2, NHC(O)NHR32, NHC(O)N(R32)2, NR32C(O)N(R32)2, OH, (O), C(O)OH, CN, NH2, CF3, OCF3, CF2CF3, F, Cl, Br or I;
R32 is R33, R34 or R35;
R33 is phenyl which is unfused or fused with benzene, heteroarene or R33A; R33A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R34 is heteroaryl which is unfused or fused with benzene, heteroarene or R34A; R34A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R35 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene, heteroarene or R35A; R35A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
D1 is N, CH or C(D2);
D2 is R36, R37, R38 or R39;
R36 is phenyl which is unfused or fused with benzene, heteroarene or R36A; R36A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R37 is heteroaryl which is unfused or fused with benzene, heteroarene or R37A; R37A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R38 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene, heteroarene or R38A; R38A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R39 is alkyl, alkenyl or alkynyl, each of which is substituted with one or two of independently selected R40, OR40, SR40, S(O)R40, SO2R40, NH2, NHR40, N(R40)2, C(O)R40, C(O)NH2, C(O)NHR40, C(O)N(R40)2, NHC(O)R40, NR40C(O)R40, NHSO2R40, NR40SO2R40, NHC(O)OR40, NR40C(O)OR40, SO2NH2, SO2NHR40, SO2N(R40)2, NHC(O)NH2, NHC(O)NHR40, NHC(O)N(R40)2, NR40C(O)N(R40)2, OH, (O), C(O)OH, CN, NH2, CF3, OCF3, CF2CF3, F, Cl, Br or I;
R40 is R41, R42 or R43;
R41 is phenyl which is unfused or fused with benzene, heteroarene or R41A; R41A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R42 is heteroaryl which is unfused or fused with benzene, heteroarene or R42A; R42A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R43 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene, heteroarene or R43A; R43A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
wherein each foregoing cyclic moiety is independently unsubstituted or substituted or further unsubstituted or further substituted with one or two or three or four of independently selected R44, OR44, SR44, S(O)R44, SO2R44, NH2, NHR44, N(R44)2, C(O)OR44, C(O)NH2, C(O)NHR44, C(O)N(R44)2, NHC(O)R44, NR44C(O)R44, NHSO2R44, NR44SO2R44, NHC(O)OR44, NR44C(O)OR44, SO2NH2, SO2NHR44, SO2N(R44)2, NHC(O)NH2, NHC(O)NHR44, NHC(O)N(R44)2, NR44C(O)N(R44)2, C(N)NH2, C(N)NHR44, C(N)N(R44)2, NHC(N)NH2, NHC(N)NHR44, NHC(N)N(R44)2, OH, (O), C(O)H, C(O)OH, NO2, CN, CF3, OCF3, CF2CF3, F, Cl, Br or I;
R44 is R45, R46, R47 or R48;
R45 is phenyl which is unfused or fused with benzene, heteroarene or R45A; R45A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R46 is heteroaryl which is unfused or fused with benzene, heteroarene or R46A; R46A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R47 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene, heteroarene or R47A; R47A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R48 is alkyl, alkenyl or alkynyl, each of which is substituted with one or two of independently selected R49, OR49, SR49, S(O)R49, SO2R49, NH2, NHR49, N(R49)2, C(O)R49, C(O)NH2, C(O)NHR49, C(O)N(R49)2, NHC(O)R49, NR49C(O)R49, NHSO2R49, NR49SO2R49, NHC(O)OR49, NR49C(O)OR49, SO2NH2, SO2NHR49, SO2N(R49)2, NHC(O)NH2, NHC(O)NHR49, NHC(O)N(R49)2, NR49C(O)N(R49)2, OP(O)(OH)2, OP(O)(OH)(OR44), OP(O)(OR44)2, OH, (O), C(O)OH, CN, CF3, OCF3, CF2CF3, F, Cl, Br or I;
R49 is R50, R51, R52, alkyl, alkenyl or alkynyl;
R50 is phenyl which is unfused or fused with benzene, heteroarene or R50A; R50A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
R51 is heteroaryl which is unfused or fused with benzene, heteroarene or R51A; R51A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene; and
R52 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene, heteroarene or R52A; R52A is cycloalkane, cycloalkene, heterocycloalkane or heterocycloalkene;
wherein the moieties represented by R45, R46, R47 and R49 are independently unsubstituted or substituted with one or two or three of four of independently selected alkyl, alkenyl, alkynyl, OH, (O), C(O)OH, CN, CF3, OCF3, CF2CF3, F. Cl, Br or I.
Another embodiment comprises compounds having formula (I), and therapeutically acceptable salts, prodrugs and salts of prodrugs thereof, wherein A1 is C(O)NHR1, C(O)N(R1)2, NHC(O)R1, NR1C(O)R1, NHC(O)NHR1, NHC(O)N(R1)2, NR1C(O)NHR1, NR1C(O)N(R1)2, SO2NHR1, SO2N(R1)2, NHSO2R1, NR1SO2R1, OC(O)OR1, NHC(O)OR1, NR1C(O)OR1 or R5;
R1 is R2, R3 or R4;
R2 is phenyl which is unfused or fused with benzene or heteroarene;
R3 is heteroaryl which is unfused or fused with benzene or heteroarene;
R4 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene or heteroarene;
R5 is alkyl, alkenyl or alkynyl, each of which is substituted with one or two of independently selected R6, OR6, SR6, S(O)R6, SO2R6, NH2, NHR6, N(R6)2, C(O)R6, C(O)NH2, C(O)NHR6, C(O)N(R6)2, NHC(O)R6, NR6C(O)R6, NHC(O)NHR6, OH, (O), C(O)OH, CN, NH2, CF3, OCF3, CF2CF3, F, Cl, Br or I;
R6 is R7, R8 or R9;
R7 is phenyl which is unfused or fused with benzene or heteroarene;
R8 is heteroaryl which is unfused or fused with benzene or heteroarene:
R9 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene or heteroarene;
wherein the moieties represented by R1, R2, R3, R4, R5 and R6 are independently substituted with one or two of independently selected R10, OR10, SR10, S(O)R10, SO2R10, NH2, NHR10, N(R10)2, C(O)R10, C(O)OR10, C(O)NHR10, C(O)N(R10)2, NHC(O)R10, NR10C(O)R10 or NHC(O)NHR10;
R10 is R11, R12, R13 or R14;
R11 is phenyl which is unfused or fused with benzene or heteroarene;
R12 is heteroaryl which is unfused or fused with benzene or heteroarene;
R13 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene or heteroarene;
R14 is alkyl, alkenyl or alkynyl, each of which is unsubstituted or substituted with one or two of independently selected R15 or NHC(O)NHR15;
R15 is R16, R17, R18;
R16 is phenyl which is unfused or fused with benzene or heteroarene;
R17 is heteroaryl which is unfused or fused with benzene or heteroarene;
R18 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene or heteroarene;
B1 is H or R19;
R19 is R20, R21, R22 or R23;
R20 is phenyl which is unfused or fused with benzene or heteroarene;
R21 is heteroaryl which is unfused or fused with benzene or heteroarene;
R22 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene or heteroarene;
R23 is alkyl, alkenyl or alkynyl, each of which is unsubstituted or substituted with one or two of independently selected R24, OR24, N(R24)2, C(O)N(R24)2, NHC(O)R24, NR24C(O)R24;
R24 is alkyl, alkenyl or alkynyl;
C1 is O, S, S(O), SO2, NH, or N(C2);
C2 is R28, R29 or R30;
R28 is phenyl which is unfused or fused with benzene or heteroarene;
R29 is heteroaryl which is unfused or fused with benzene or heteroarene;
R30 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene or heteroarene;
D1 is N, CH or C(D2);
D2 is R36, R37 or R38;
R36 is phenyl which is unfused or fused with benzene or heteroarene;
R37 is heteroaryl which is unfused or fused with benzene or heteroarene;
R38 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene or heteroarene;
wherein each foregoing cyclic moiety is independently unsubstituted or substituted or further unsubstituted or further substituted with one or two or three or four of independently selected R44, OR44, SR44, S(O)R44, SO2R44, NH2, NHR44, N(R44)2, C(O)R44, C(O)OR44, C(O)NH2, C(O)NHR44, C(O)N(R44)2, NHC(O)R44, OH, (O), C(O)H, C(O)OH, NO2, CN, CF3, OCF3, CF2CF3, F, Cl, Br or I;
R44 is R45, R46, R47 or R48;
R45 is phenyl which is unfused or fused with benzene or heteroarene;
R46 is heteroaryl which is unfused or fused with benzene or heteroarene;
R47 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene or heteroarene;
R48 is alkyl substituted with OP(O)(OH)2;
wherein the moieties represented by R45, R46 and R47 are independently unsubstituted or substituted with one or two or three or four of independently selected alkyl, alkenyl, alkynyl, OH, (O), C(O)OH, CN, CF3, OCF3, CF2CF3, F, Cl, Br or I.
Still another embodiment comprises compounds having formula (I), and therapeutically acceptable salts, prodrugs and salts of prodrugs thereof, wherein A1 is C(O)NHR1 or R5;
R1 is R2, R3 or R4;
R2 is phenyl which is unfused or fused with benzene or heteroarene;
R3 is heteroaryl which is unfused or fused with benzene or heteroarene;
R4 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene or heteroarene;
R5 is alkyl, alkenyl or alkynyl, each of which is substituted with one or two of independently selected R6, NHC(O)NHR6;
R6 is R7, R8 or R9;
R7 is phenyl which is unfused or fused with benzene or heteroarene;
R8 is heteroaryl which is unfused or fused with benzene or heteroarene;
R9 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene or heteroarene;
wherein the moieties represented by R1, R2, R3, R4, R5 and R6 are independently substituted with one or two of independently selected R10, OR10, SR10, S(O)R10, SO2R10, NH2, NHC(O)R10, NHC(O)NHR10;
R10 is R11, R12, R13 or R14;
R11 is phenyl which is unfused or fused with benzene or heteroarene;
R12 is heteroaryl which is unfused or fused with benzene or heteroarene;
R13 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene or heteroarene;
R14 is alkyl, alkenyl or alkynyl, each of which is unsubstituted or substituted with one or two of independently selected R15 or NHC(O)NHR15;
R15 is R16, R17 R18;
R16 is phenyl which is unfused or fused with benzene or heteroarene;
R17 is heteroaryl which is unfused or fused with benzene or heteroarene;
R18 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene or heteroarene;
B1 is H or R19;
R19 is R20, R21, R22 or R23;
R20 is phenyl which is unfused or fused with benzene or heteroarene;
R21 is heteroaryl which is unfused or fused with benzene or heteroarene;
R22 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused with benzene or heteroarene;
R23 is alkyl, alkenyl or alkynyl, each of which is unsubstituted or substituted with one or two of independently selected R24, OR24 or N(R24)2;
R24 is alkyl, alkenyl or alkynyl;
C1 is O, S, S(O), SO2, NH, or N(C2);
C2 is R28, R29 or R30;
R28 is phenyl which is unfused or fused with benzene or heteroarene;
R29 is heteroaryl which is unfused or fused with benzene or heteroarene;
R30 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene or heteroarene;
D1 is N, CH or C(D2);
D2 is R36, R37 or R38;
R36 is phenyl which is unfused or fused with benzene or heteroarene;
R37 is heteroaryl which is unfused or fused with benzene or heteroarene;
R38 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene or heteroarene;
wherein each foregoing cyclic moiety is independently unsubstituted or substituted or further unsubstituted or further substituted with one or two or three or four of independently selected R44, OR44, CN, CF3, OCF3, CF2CF3, F, Cl, Br or I;
R44 is R45, R46, R47 or R48;
R45 is phenyl which is unfused or fused with benzene or heteroarene;
R46 is heteroaryl which is unfused or fused with benzene or heteroarene;
R47 is cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl, each of which is unfused or fused with benzene or heteroarene;
R48 is alkyl substituted with OP(O)(OH)2;
wherein the moieties represented by R45, R46, and R47 are independently unsubstituted or substituted with one or two or three of four of independently selected alkyl.
Still another embodiment comprises compounds having formula (I), and therapeutically acceptable salts, prodrugs and salts of prodrugs thereof, wherein A1 is C(O)NHR1 or R5;
R1 is R2, R3 or R4;
R2 is phenyl;
R3 is heteroaryl;
R4 is cycloalkyl or heterocycloalkyl;
R5 is alkyl, alkenyl or alkynyl, each of which is substituted with R6, NHC(O)NHR6;
R6 is R7 or R9;
R7 is phenyl;
R8 is heteroaryl;
R9 is heterocycloalkyl;
wherein the moieties represented by R1, R2, R3, R4, R5 and R6 are independently substituted with one or two of independently selected R10, OR10, SR10, SO2R10, NH2, NHC(O)R10, NHC(O)NHR10;
R10 is R11, R12, R13 or R14;
R11 is phenyl;
R12 is heteroaryl;
R13 is cycloalkyl;
R14 is alkyl which is unsubstituted or substituted with R16 or NHC(O)NHR16;
R16 is phenyl;
B1 is H or R19;
R19 is R21, R22 or R23;
R21 is heteroaryl;
R22 is heterocycloalkyl;
R23 is alkynyl, which is unsubstituted or substituted with R24, OR24 or N(R24)2;
R24 is alkyl;
C1 is S or N(C2);
C2 is R30;
R30 is cycloalkyl;
D1 is N, CH or C(D2);
D2 is R37;
R37 is heteroaryl;
wherein each foregoing cyclic moiety is independently unsubstituted or substituted or further unsubstituted or further substituted with one or two or three or four of independently selected R44, OR44, CN, CF3, F, Cl, Br or I;
R44 is R47 or R48;
R47 is heterocycloalkyl;
R48 is alkyl substituted with OP(O)(OH)2;
wherein R47 is unsubstituted or substituted with alkyl.
Still another embodiment pertains to compositions comprising an excipient and a therapeutically effective amount of a compound having formula (I).
Still another embodiment pertains to methods of treating diseases involving overexpression or unregulation of Protein kinases in a mammal, the methods comprising administering thereto a therapeutically effective amount of a compound having formula (I).
Still another embodiment pertains to methods of treating cancer in a mammal comprising administering thereto a therapeutically effective amount of a compound having formula (I).
Still another embodiment pertains to methods of treating bladder cancer, breast cancer, cervical cancer, colon cancer, endometrial cancer, esophageal cancer, lung cancer, ovarian cancer, pancreatic cancer, prostate cancer, rectal cancer, skin cancer, stomach cancer and thyroid cancer in a mammal, the methods comprising administering thereto a therapeutically effective amount of a compound having formula (I).
Still another embodiment pertains to compositions comprising an excipient and a therapeutically effective amount of a compound having formula (I) and a therapeutically effective amount of one additional therapeutic agent or more than one additional therapeutic agent.
Still another embodiment pertains to methods of treating diseases involving overexpression or unregulation of protein kinases in a mammal, the methods comprising administering thereto a therapeutically effective amount of a compound having formula (I) and a therapeutically effective amount of one additional therapeutic agent or more than one additional therapeutic agent, with or without radiation.
Still another embodiment pertains to methods of treating bladder cancer, breast cancer, cervical cancer, colon cancer, endometrial cancer, esophageal cancer, leukemia, lymphoma, lung cancer, ovarian cancer, pancreatic cancer, prostate cancer, rectal cancer, skin cancer, stomach cancer or thyroid cancer in a mammal, the methods comprising administering thereto a therapeutically effective amount of a compound having formula (I) and a therapeutically effective amount of one additional therapeutic agent or more than one additional therapeutic agent.
Still another embodiment pertains to
4-amino-N-(4-((3-toluidinocarbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((3-fluoroanilino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((3-fluoro-4-methylanilino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((4-toluidinocarbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((4-fluoroanilino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((3-chloro-4-fluoroanilino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((3-ethylanilino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((3-chloroanilino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((3-cyanoanilino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((2-fluoroanilino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((3-(trifluoromethyl)anilino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((4-fluoro-3-(trifluoromethyl)anilino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((3-methoxyanilino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((5-fluoro-2-methylanilino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((4-(trifluoromethyl)anilino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((2-fluoro-5-methylanilino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((2-toluidinocarbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((4-methoxyanilino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((3,5-dimethylanilino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((2-fluoro-5-(trifluoromethyl)anilino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((anilinocarbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((3-chloroanilino)carbonyl)amino)phenyl)-6-(1-methyl-1H-pyrazol-4-yl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-6-(1-methyl-1H-pyrazol-4-yl)-N-(4-((3-toluidinocarbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide
4-amino-N-(4-(((2-fluoro-5-methylanilino)carbonyl)amino)phenyl)-6-(1-methyl-1H-pyrazol-4-yl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((4-fluoro-3-(trifluoromethyl)anilino)carbonyl)amino)phenyl)-6-(1-methyl-1H-pyrazol-4-yl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((2-fluoro-5-(trifluoromethyl)anilino)carbonyl)amino)phenyl)-6-(1-methyl-1H-pyrazol-4-yl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-6-(1-methyl-1H-pyrazol-4-yl)-N-(4-(((4-(trifluoromethyl)anilino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-6-(1-methyl-1H-pyrazol-4-yl)-N-(4-phenoxyphenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-phenoxyphenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(3-methylphenoxy)phenyl)-6-(1-methyl-1H-pyrazol-4-yl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(4-chlorophenoxy)phenyl)-6-(1-methyl-1H-pyrazol-4-yl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(4-methylphenoxy)phenyl)-6-(1-methyl-1H-pyrazol-4-yl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(3-chlorophenoxy)phenyl)-6-(1-methyl-1H-pyrazol-4-yl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-6-(1-methyl-1H-pyrazol-4-yl)-N-(4-(phenylsulfanyl)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(4-methylphenoxy)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-phenoxyphenyl)-6-(1H-pyrazol-4-yl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-phenoxyphenyl)-6-(3-thienyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-6-(4-methyl-1-piperazinyl)-N-(4-((3-toluidinocarbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-methyl-N-(4-((3-toluidinocarbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-phenoxyphenyl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(3-phenoxyphenyl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(4-benzylphenyl)thieno [3,2-c]pyridine-3-carboxamide,
4-amino-N-(4-((3-toluidinocarbonyl)amino)phenyl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(4-(benzoylamino)phenyl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-7-(1-methyl-1H-pyrazol-4-yl)-N-(4-((3-toluidinocarbonyl)amino)phenyl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(4-(benzoylamino)phenyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-7-(1-methyl-1H-pyrazol-4-yl)-N-(4-phenoxyphenyl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-7-(1-methyl-1H-pyrazol-4-yl)-N-(3-phenoxyphenyl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(4-benzylphenyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-7-(4-(4-methyl-1-piperazinyl)cyclohexyl)-N-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxamide,
4-amino-7-(4-(4-methyl-1-piperazinyl)cyclohexyl)-N-(3-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxamide,
4-amino-7-(4-(4-methyl-1-piperazinyl)cyclohexyl)-N-(4-((3-toluidinocarbonyl)amino)phenyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((4-aminophenyl)sulfanyl)phenyl)-7-(4-(4-methyl-1-piperazinyl)cyclohexyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-benzylphenyl)-7-(4-(4-methyl-1-piperazinyl)cyclohexyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxamide,
4-amino-7-(4-(4-methyl-1-piperazinyl)cyclohexyl)-N-(4-(phenylsulfonyl)phenyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxamide,
4-amino-1-(4-(4-morpholinyl)cyclohexyl)-1H-pyrazolo(3,4-d)pyrimidine-3-carboxylic acid,
4-amino-1-(4-(4-morpholinyl)cyclohexyl)-N-(4-phenoxyphenyl)-1H-pyrazolo(3,4-d)pyrimidine-3-carboxamide,
N-(4-((E)-2-(4-amino-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridin-3-yl)ethenyl)phenyl)-N′-(3-methylphenyl)urea
7-(1-methyl-1H-pyrazol-4-yl)-3-((E)-2-(4-phenoxyphenyl)ethenyl)thieno[3,2-c]pyridin-4-amine,
3-((E)-2-(1,1′-biphenyl)-4-ylethenyl)-7-( i-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridin-4-amine,
4-amino-N-(4-((anilinocarbonyl)amino)phenyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine -3-carboxamide,
4-amino-N-(4-((((3-fluorophenyl)amino)carbonyl)amino)phenyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(4-(((cyclohexylamino)carbonyl)amino)phenyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(4-((((4-methylphenyl)amino)carbonyl)amino)phenyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(4-((((2-methylphenyl)amino)carbonyl)amino)phenyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(3-((anilinocarbonyl)amino)phenyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(3-((((2-methylphenyl)amino)carbonyl)amino)phenyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(3-((((4-methylphenyl)amino)carbonyl)amino)phenyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(3-((((3-methylphenyl)amino)carbonyl)amino)phenyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(3-(benzoylamino)phenyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(1-(anilinocarbonyl)piperidin-4-yl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(1-benzoylpiperidin-4-yl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
trans4-amino-N-(4-(benzoylamino)cyclohexyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
trans4-amino-N-(4-((anilinocarbonyl)amino)cyclohexyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
trans4-amino-N-(4-((((2-fluorophenyl)amino)carbonyl)amino)cyclohexyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(4-((anilinocarbonyl)amino)benzyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(3-((anilinocarbonyl)amino)benzyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-((1-(anilinocarbonyl)piperidin-4-yl)methyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(4-(((anilinocarbonyl)amino)methyl)phenyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(3-(((anilinocarbonyl)amino)methyl)phenyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
cis-4-amino-N-(4-((anilinocarbonyl)amino)cyclohexyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
cis-4-amino-N-((1S,3R)-3-((anilinocarbonyl)amino)cyclohexyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
cis-4-amino-N-((1S,3R)-3-(anilinocarbonyl)cyclohexyl)-7-(1-methyl-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
4-amino-N-(3-(((anilinocarbonyl)amino)methyl)phenyl)-7-(1-(2-hydroxyethyl)-1H-pyrazol-4-yl)thieno[3,2-c]pyridine-3-carboxamide,
2-(4-(4-amino-3-(((3-(((anilinocarbonyl)amino)methyl)phenyl)amino)carbonyl)thieno[3,2-c]pyridin-7-yl)-1H-pyrazol-1-yl)ethyl dihydrogen phosphate,
4-amino-N-(4-((((2-fluoro-3-(trifluoromethyl)phenyl)amino)carbonyl)amino)phenyl)-6-(1-methyl-1H-pyrazol-4-yl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((anilinocarbonyl)amino)phenyl)-6-(1-methyl-1H-pyrazol-4-yl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((anilinocarbonyl)amino)phenyl)-6-thien-3-ylthieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((anilinocarbonyl)amino)phenyl)-6-morpholin-4-ylthieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((thien-3-ylamino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((cyclopentylamino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((pyridin-3-ylamino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((((5-methylisoxazol-3-yl)amino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((cyclopropylamino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((((2,4-difluorophenyl)amino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((((3,4-difluorophenyl)amino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((((3-(morpholin-4-ylmethyl)phenyl)amino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((anilinocarbonyl)amino)cyclohexyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((((3,5-dimethylisoxazol-4-yl)amino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((1,3-thiazol-2-ylamino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-(((isoxazol-3-ylamino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(1-(anilinocarbonyl)piperidin-4-yl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(3-((anilinocarbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((anilinocarbonyl)amino)phenyl)-6-(3-methoxyprop-1-ynyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((anilinocarbonyl)amino)phenyl)-6-ethynylthieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((anilinocarbonyl)amino)phenyl)-6-(thien-3-ylethynyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((anilinocarbonyl)amino)phenyl)-6-(3-(dimethylamino)prop-1-ynyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((2-fluorobenzoyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino -N-(4-((3-fluorobenzoyl)amino)phenyl)thieno [2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((4-fluorobenzoyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((2-methylbenzoyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((3-methylbenzoyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((((3-(hydroxymethyl)phenyl)amino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(3-(((anilinocarbonyl)amino)methyl)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(3-((((2-methylphenyl)amino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(3-(((((3-methylphenyl)amino)carbonyl)amino)methyl)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(3-(((((3-fluorophenyl)amino)carbonyl)amino)methyl)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(3-((((3-methylphenyl)amino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(3-((((4-methylphenyl)amino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(3-((((2-fluorophenyl)amino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(3-((((3-fluorophenyl)amino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(3-((((4-fluorophenyl)amino)carbonyl)amino)phenyl)thieno [2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(3-(((((3-(trifluoromethyl)phenyl)amino)carbonyl)amino)methyl)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(5-(2-((3-fluorophenyl)amino)-2-oxoethyl)-1,3-thiazol-2-yl)thieno[2,3-d]pyrimidine-5-carboxamide,
N-(4-(2-(4-aminothieno[2,3-d]pyrimidin-5-yl)ethyl)phenyl)-N′-phenylurea,
4-amino-N-(4-((((3-(3-hydroxypropoxy)phenyl)amino)carbonyl)amino)phenyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((anilinocarbonyl)amino)benzyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((((3-methylphenyl)amino)carbonyl)amino)benzyl)thieno[2,3-d]pyrimidine-5-carboxamide,
4-amino-N-(4-((((3-fluorophenyl)amino)carbonyl)amino)benzyl)thieno[2,3-d]pyrimidine-5-carboxamide
and therapeutically acceptable salts, prodrugs, salts of prodrugs and metabolites thereof.
Variable moieties of compounds herein are represented by identifiers (capital letters with numerical and/or alphabetical superscripts) and may be specifically embodied.
It is meant to be understood that proper valences are maintained for all moieties and combinations thereof, that monovalent moieties having more than one atom are attached through their left ends.
It is also meant to be understood that a specific embodiment of a variable moiety may be the same or different as another specific embodiment having the same identifier.
The term “cyclic moiety,” as used herein, means benzene, cycloalkane, cycloalkyl, cycloalkene, cycloalkenyl, heteroarene, heteroaryl, heterocycloalkane, heterocycloalkyl, heterocycloalkene, heterocycloalkenyl, phenyl, spiroalkyl, spiroalkenyl, spiroheteroalkyl and spiroheteroalkenyl.
The term “cycloalkane,” as used herein, means C3-cycloalkane, C4-cycloalkane, C5-cycloalkane and C6-cycloalkane.
The term “cycloalkyl,” as used herein, means C3-cycloalkyl, C4-cycloalkyl, C5-cycloalkyl and C6-cycloalkyl.
The term “cycloalkene,” as used herein, means C4-cycloalkene, C5-cycloalkene and C6-cycloalkene.
The term “cycloalkenyl,” as used herein, means C4-cycloalkenyl, C5-cycloalkenyl and C6-cycloalkenyl.
The term “heteroarene,” as used herein, means furan, imidazole, isothiazole, isoxazole, 1,2,3-oxadiazole, 1,2,5-oxadiazole, oxazole, pyrazine, pyrazole, pyridazine, pyridine, pyrimidine, pyrrole, thiazole, thiophene, triazine and 1,2,3-triazole.
The term “heteroaryl,” as used herein, means furanyl, imidazolyl, isothiazolyl, isoxazolyl, 1,2,3-oxadiazoyl, 1,2,5-oxadiazolyl, oxazolyl, pyrazinyl, pyrazolyl, pyridazinyl, pyridinyl, pyrimidinyl, pyrrolyl, tetrazolyl, thiazolyl, thiophenyl, triazinyl and 1,2,3-triazolyl.
The term “heterocycloalkane,” as used herein, means cycloalkane having one or two or three CH2 moieties replaced with independently selected O, S, S(O), SO2 or NH and one or two CH moieties unreplaced or replaced with N and also means cycloalkane having one or two or three CH2 moieties unreplaced or replaced with independently selected O, S, S(O), SO2 or NH and one or two CH moieties replaced with N.
The term “heterocycloalkyl,” as used herein, means cycloalkyl having one or two or three CH2 moieties replaced with independently selected O, S, S(O), SO2 or NH and one or two CH moieties unreplaced or replaced with N and also means cycloalkyl having one or two or three CH2 moieties unreplaced or replaced with independently selected O, S, S(O), SO2 or NH and one or two CH moieties replaced with N.
The term “heterocycloalkene,” as used herein, means cycloalkene having one or two or three CH2 moieties replaced with independently selected O, S, S(O), SO2 or NH and one or two CH moieties unreplaced or replaced with N and also means cycloalkene having one or two or three CH2 moieties unreplaced or replaced with independently selected O, S, S(O), SO2 or NH and one or two CH moieties replaced with N.
The term “heterocycloalkenyl,” as used herein, means cycloalkenyl having one or two or three CH2 moieties replaced with independently selected O, S, S(O), SO2 or NH and one or two CH moieties unreplaced or replaced with N and also means cycloalkenyl having one or two or three CH2 moieties unreplaced or replaced with independently selected O, S, S(O), SO2 or NH and one or two CH moieties replaced with N.
The term “alkenyl,” as used herein, means C2-alkenyl, C3-alkenyl, C4-alkenyl, C5-alkenyl and C6-alkenyl.
The term “alkyl,” as used herein, means C1-alkyl, C2-alkyl, C3-alkyl, C4-alkyl, C5-alkyl and C6-alkyl.
The term “alkynyl,” as used herein, means C2-alkynyl, C3-alkynyl, C4-alkynyl, C5-alkynyl and C6-alkynyl.
The term “C2-alkenyl,” as used herein, means ethenyl (vinyl).
The term “C3-alkenyl,” as used herein, means 1-propen-1-yl, 1-propen-2-yl (isopropenyl) and 1-propen-3-yl (allyl).
The term “C4-alkenyl,” as used herein, means 1-buten-1-yl, 1-buten-2-yl, 1,3-butadien-1-yl, 1,3-butadien-2-yl, 2-buten-1-yl, 2-buten-2-yl, 3-buten-1-yl, 3-buten-2-yl, 2-methyl-1-propen-1-yl and 2-methyl-2-propen-1-yl.
The term “C5-alkenyl,” as used herein, means 2-methylene-3-buten-1-yl, 2-methylenebut-1-yl, 2-methyl-1-buten-1-yl, 2-methyl-1,3-butadien-1-yl, 2-methyl-2-buten-1-yl, 2-methyl-3-buten-1-yl, 2-methyl-3-buten-2-yl, 3-methyl-1-buten-1-yl, 3-methyl-1-buten-2-yl, 3-methyl-1,3-butadien-1-yl, 3-methyl-1,3-butadien-2-yl, 3-methyl-2-buten-1-yl, 3-methyl-2-buten-2-yl, 3-methyl-3-buten-1-yl, 3-methyl-3-buten-2-yl, 1-penten-1-yl, 1-penten-2-yl, 1-penten-3-yl, 1,3-pentadien-1-yl, 1,3-penta-dien-2-yl, 1,3-pentadien-3-yl, 1,4-pentadien-1-yl, 1,4-pentadien-2-yl, 1,4-pentadien-3-yl, 2-penten-1-yl, 2-penten-2-yl, 2-penten-3-yl, 2,4-pentadien-1-yl, 2,4-pentadien-2-yl, 3-penten-1-yl, 3-penten-2-yl, 4-penten-1-yl and 4-penten-2-yl.
The term “C6-alkenyl,” as used herein, means 2,2-dimethyl-3-buten-1-yl, 2,3-dimethyl-1-buten-1-yl, 2,3-dimethyl-1,3-butadien-1-yl, 2,3-dimethyl-2-buten-1-yl, 2,3-dimethyl-3-buten-1-yl, 2,3-dimethyl-3-buten-2-yl, 3,3-dimethyl-1-buten-1-yl, 3,3-dimethyl-1-buten-2-yl, 2-ethenyl-1,3-butadien-1-yl, 2-ethenyl-2-buten-1-yl, 2-ethyl-1-buten-1-yl, 2-ethyl-1,3-butadien-1-yl, 2-ethyl-2-buten-1-yl, 2-ethyl-3-buten-1-yl, 1-hexen-1-yl, 1-hexen-2-yl, 1-hexen-3-yl, 1,3-hexadien-1-yl, 1,3-hexadien-2-yl, 1,3-hexadien-3-yl, 1,3,5-hexatrien-1-yl, 1,3,5-hexatrien-2-yl, 1,3,5-hexatrien-3-yl, 1,4-hexadien-1-yl, 1,4-hexadien-2-yl, 1,4-hexadien-3-yl, 1,5-hexadien-1-yl, 1,5-hexadien-2-yl, 1,5-hexadien-3-yl, 2-hexen-1-yl, 2-hexen-2-yl, 2-hexen-3-yl, 2,4-hexadien-1-yl, 2,4-hexadien-2-yl, 2,4-hexadien-3-yl, 2,5-hexadien-1-yl, 2,5-hexadien-2-yl, 2,5-hexadien-3-yl, 3-hexen-1-yl, 3-hexen-2-yl, 3-hexen-3-yl, 3,5-hexadien-1-yl, 3,5-hexadien-2-yl, 3,5-hexadien-3-yl, 4-hexen-1-yl, 4-hexen-2-yl, 4-hexen-3-yl, 5-hexen-1-yl, 5-hexen-2-yl, 5-hexen-3-yl, 2-methylene-3-methyl-3-buten-1-yl, 2-methylene-3-methylbut-1-yl, 2-methylene-3-penten-1-yl, 2-methylene-4-penten-1-yl, 2-methylenepent-1-yl, 2-methylenepent-3-yl, 3-methylene-1-penten-1-yl, 3-methylene-1-penten-2-yl, 3-methylenepent-1-yl, 3-methylene-1,4-pentadien-1-yl, 3-methylene-1,4-pentadien-2-yl, 3-methylene-pent-2-yl, 2-methyl-1-penten-1-yl, 2-methyl-1-penten-3-yl, 2-methyl-1,3-pentadien-1-yl, 2-methyl-1,3-pentadien-3-yl, 2-methyl-1,4-pentadien-1-yl, 2-methyl-1,4-pentadien-3-yl, 2-methyl-2-penten-1-yl, 2-methyl-2-penten-3-yl, 2-methyl-2,4-pentadien-1-yl, 2-methyl-2,4-pentadien-3-yl, 2-methyl-3-penten-1-yl, 2-methyl-3-penten-2-yl, 2-methyl-3-penten-3-yl, 2-methyl-4-penten-1-yl, 2-methyl-4-penten-2-yl, 2-methyl-4-penten-3-yl, 3-methyl-1-penten-1-yl, 3-methyl-1-penten-2-yl, 3-methyl-1,3-pentadien-1-yl, 3-methyl-1,3-pentadien-2-yl, 3-methyl-1,4-pentadien-1-yl, 3-methyl-1,4-pentadien-2-yl, 3-methyl-2-penten-1-yl, 3-methyl-2-penten-2-yl, 3-methyl-2,4-pentadien-1-yl, 3-methyl-3-penten-1yl, 3-methyl-3-penten-2-yl, 3-methyl-4-penten-1-yl, 3-methyl-4-penten-2-yl, 3-methyl-4-penten-3-yl, 4-methyl-1-penten-1-yl, 4-methyl-1-penten-2-yl, 4-methyl-1-penten-3-yl, 4-methyl-1,3-pentadien-1-yl, 4-methyl-1,3-pentadien-2-yl, 4-methyl-1,3-pentadien-3-yl, 4-methyl-1,4-pentadien-1-yl, 4-methyl-1,4-pentadien-2-yl, 4-methyl-1,4-pentadien-3-yl, 4-methylene-2-penten-3-yl, 4-methyl-2-penten-1-yl, 4-methyl-2-penten-2-yl, 4-methyl-2-penten-3-yl, 4-methyl-2,4-pentadien-1-yl, 4-methyl-2,4-pentadien-2-yl, 4-methyl-3-penten-1-yl, 4-methyl-3-penten-2-yl, 4-methyl-3-penten-3-yl, 4-methyl-4-penten-1-yl and 4-methyl-4-penten-2-yl,
The term “C1-alkyl,” as used herein, means methyl.
The term “C2-alkyl,” as used herein, means ethyl.
The term “C3-alkyl,” as used herein, means prop-1-yl and prop-2-yl (isopropyl).
The term “C4-alkyl,” as used herein, means but-1-yl, but-2-yl, 2-methylprop-1-yl and 2-methylprop-2-yl (tert-butyl).
The term “C5-alkyl,” as used herein, means 2,2-dimethylprop-1-yl (neo-pentyl), 2-methylbut-1-yl, 2-methylbut-2-yl, 3-methylbut-1-yl, 3-methylbut-2-yl, pent-1-yl, pent-2-yl and pent-3-yl.
The term “C6-alkyl,” as used herein, means 2,2-dimethylbut-1-yl, 2,3-dimethylbut-1-yl, 2,3-dimethylbut-2-yl, 3,3-dimethylbut-1-yl, 3,3-dimethylbut-2-yl, 2-ethylbut-1-yl, hex-1-yl, hex-2-yl, hex-3-yl, 2-methylpent-1-yl, 2-methylpent-2-yl, 2-methylpent-3-yl, 3-methylpent-1-yl, 3-methylpent-2-yl, 3-methylpent-3-yl, 4-methylpent-1-yl and 4-methylpent-2-yl.
The term “C2-alkynyl,” as used herein, means ethynyl (acetylenyl).
The term “C3-alkynyl,” as used herein, means 1-propyn-1-yl and 2-propyn-1-yl (propargyl).
The term “C4-alkynyl,” as used herein, means 1-butyn-1-yl, 1,3-butadiyn-1-yl, 2-butyn-1-yl, 3-butyn-1-yl and 3-butyn-2-yl.
The term “C5-alkynyl,” as used herein, means 2-methyl-3-butyn-1-yl, 2-methyl-3-butyn-2-yl, 3-methyl-1-butyn-1-yl, 1,3-pentadiyn-1-yl, 1,4-pentadiyn-1-yl, 1,4-pentadiyn-3-yl, 2,4-pentadiyn-1-yl, 1-pentyn-1-yl, 1-pentyn-3-yl, 2-pentyn-1-yl, 3-pentyn-1-yl, 3-pentyn-2-yl, 4-pentyn-1-yl and 4-pentyn-2-yl.
The term “C6-alkynyl,” as used herein, means 2,2-dimethyl-3-butyn-1-yl, 3,3-dimethyl-1-butyn-1-yl, 2-ethyl-3-butyn-1-yl, 2-ethynyl-3-butyn-1-yl, 1-hexyn-1-yl, 1-hexyn-3-yl, 1,3-hexadiyn-1-yl, 1,3,5-hexatriyn-1-yl, 1,4-hexadiyn-1-yl, 1,4-hexadiyn-1-yl, 1,4-hexadiyn-3-yl, 1,5-hexadiyn-1-yl, 1,5-hexadiyn-3-yl, 2-hexyn-1-yl, 2,5-hexadiyn-1-yl, 3-hexyn-1-yl, 3-hexyn-2-yl, 3,5-hexadiyn-2-yl, 4-hexyn-1-yl, 4-hexyn-2-yl, 4-hexyn-3-yl, 5-hexyn-1-yl, 5-hexyn-2-yl, 5-hexyn-3-yl, 2-methyl-3-pentyn-1-yl, 2-methyl-3-pentyn-2-yl, 2-methyl-4-pentyn-1-yl, 2-methyl-4-pentyn-2-yl, 2-methyl-4-pentyn-3-yl, 3-methyl-1-pentyn-1-yl, 3-methyl-4-pentyn-1-yl, 3-methyl-4-pentyn-2-yl, 3-methyl-1,4-pentadiyn-1-yl, 3-methyl-1,4-pentadiyn-3-yl, 3-methyl-4-pentyn-1-yl, 3-methyl-4-pentyn-3-yl, 4-methyl-1-pentyn-1-yl and 4-methyl-2-pentyn-1-yl.
The term “C4-cycloalkane,” as used herein, means cyclobutane.
The term “C5-cycloalkane,” as used herein, means cyclopentane.
The term “C6-cycloalkane,” as used herein, means cyclohexane.
The term “C4-cycloalkene,” as used herein, means cyclobutene and 1,3-cyclobutadiene.
The term “C5-cycloalkene,” as used herein, means cyclopentene and 1,3-cyclopentadiene.
The term “C6-cycloalkene,” as used herein, means cyclohexene, 1,3-cyclohexadiene and 1,4-cyclohexadiene.
The term “C3-cycloalkenyl,” as used herein, means cycloprop-1-en-1-yl and cycloprop-2-en-1-yl.
The term “C4-cycloalkenyl,” as used herein, means cyclobut-1-en-1-yl and cyclobut-2-en-1-yl.
The term “C5-cycloalkenyl,” as used herein, means cyclopent-1-en-1-yl, cyclopent-2-en-1-yl, cyclopent-3-en-1-yl and cyclopenta-1,3-dien-1-yl.
The term “C6-cycloalkenyl,” as used herein, means cyclohex-1-en-1-yl, cyclohex-2-en-1-yl, cyclohex-3-en-1-yl, cyclohexa-1,3-dien-1-yl, cyclohexa-1,4-dien-1-yl, cyclohexa-1,5-dien-1-yl, cyclohexa-2,4-dien-1-yl and cyclohexa-2,5-dien-1-yl.
The term “C3-cycloalkyl,” as used herein, means cycloprop-1-yl.
The term “C4-cycloalkyl,” as used herein, means cyclobut-1-yl.
The term “C5-cycloalkyl,” as used herein, means cyclopent-1-yl.
The term “C6-cycloalkyl,” as used herein, means cyclohex-1-yl.
Compounds of this invention may contain asymmetrically substituted carbon atoms in the R or S configuration, wherein the terms “R” and “S” are as defined in Pure Appl. Chem. (1976) 45, 13-10. Compounds having asymmetrically substituted carbon atoms with equal amounts of R and S configurations are racemic at those atoms. Atoms having excess of one configuration over the other are assigned the configuration in excess, preferably an excess of about 85%-90%, more preferably an excess of about 95%-99%, and still more preferably an excess greater than about 99%. Accordingly, this invention is meant to embrace racemic mixtures and relative and absolute diastereoisomers of the compounds thereof.
Compounds of this invention may also contain carbon-carbon double bonds or carbon-nitrogen double bonds in the Z or E configuration, in which the term “Z” represents the larger two substituents on the same side of a carbon-carbon or carbon-nitrogen double bond and the term “E” represents the larger two substituents on opposite sides of a carbon-carbon or carbon-nitrogen double bond. The compounds of this invention may also exist as a mixture of “Z” and “E” isomers.
Compounds of this invention may also exist as tautomers or equilibrium mixtures thereof wherein a proton of a compound shifts from one atom to another. Examples of tautomers include, but are not limited to, keto-enol, phenol-keto, oxime-nitroso, nitro-aci, imine-enamine and the like.
Compounds of this invention containing NH, C(O)OH, OH or SH moieties may have attached thereto prodrug-forming moieties. The prodrug-forming moieties are removed by metabolic processes and release the compounds having the freed NH, C(O)OH, OH or SH in vivo. Prodrugs are useful for adjusting such pharmacokinetic properties of the compounds as solubility and/or hydrophobicity, absorption in the gastrointestinal tract, bioavailability, tissue penetration, and rate of clearance.
Metabolites of compounds having formula (I) produced by in vitro or in vivo metabolic processes, may also have utility for treating diseases associated with overexpression or unregulation of protein kinases.
Certain precursor compounds which may be metabolized in vitro or in vivo to form compounds having formula (I) may also have utility for treating diseases associated with overexpression or unregulation of protein kinases.
Compounds having formula (I) may exist as acid addition salts, basic addition salts or zwitterions. Salts of compounds having formula (I) are prepared during their isolation or following their purification. Acid addition salts are those derived from the reaction of a compound having formula (I) with acid. Accordingly, salts including the acetate, adipate, alginate, bicarbonate, citrate, aspartate, benzoate, benzenesulfonate (besylate), bisulfate, butyrate, camphorate, camphorsufonate, digluconate, formate, fumarate, glycerophosphate, glutamate, hemisulfate, heptanoate, hexanoate, hydrochloride, hydrobromide, hydroiodide, lactobionate, lactate, maleate, mesitylenesulfonate, methanesulfonate, naphthylenesulfonate, nicotinate, oxalate, pamoate, pectinate, persulfate, phosphate, picrate, propionate, succinate, tartrate, thiocyanate, trichloroacetic, trifluoroacetic, para-toluenesulfonate and undecanoate salts of the compounds having formula (I) are meant to be embraced by this invention. Basic addition salts of compounds are those derived from the reaction of the compounds having formula (I) with the bicarbonate, carbonate, hydroxide or phosphate of cations such as lithium, sodium, potassium, calcium and magnesium.
Compounds having formula (I) may be administered, for example, bucally, ophthalmically, orally, osmotically, parenterally (intramuscularly, intraperintoneally intrastemally, intravenously, subcutaneously), rectally, topically, transdermally, vaginally and intraarterially as well as by intraarticular injection, infusion, and placement in the body, such as, for example, the vasculature.
Therapeutically effective amounts of a compound having formula (I) depend on recipient of treatment, disease treated and severity thereof, composition comprising it, time of administration, route of administration, duration of treatment, potency, rate of clearance and whether or not another drug is co-administered. The amount of a compound having formula (I) used to make a composition to be administered daily to a patient in a single dose or in divided doses is from about 0.03 to about 200 mg/kg body weight. Single dose compositions contain these amounts or a combination of submultiples thereof.
Compounds having formula (I) may be administered with or without an excipient. Excipients include, but are not limited to, encapsulators and additives such as absorption accelerators, antioxidants, binders, buffers, coating agents, coloring agents, diluents, disintegrating agents, emulsifiers, extenders, fillers, flavoring agents, humectants, lubricants. perfumes, preservatives, propellants, releasing agents, sterilizing agents, sweeteners, solubilizers, wetting agents, mixtures thereof and the like.
Excipients for preparation of compositions comprising a compound having formula (I) to be administered orally include, but are not limited to, agar, alginic acid, aluminum hydroxide, benzyl alcohol, benzyl benzoate, 1,3-butylene glycol, carbomers, castor oil, cellulose, cellulose acetate, cocoa butter, corn starch, corn oil, cottonseed oil, cross-povidone, diglycerides, ethanol, ethyl cellulose, ethyl laureate, ethyl oleate, fatty acid esters, gelatin, germ oil, glucose, glycerol, groundnut oil, hydroxypropylmethyl celluose, isopropanol, isotonic saline, lactose, magnesium hydroxide, magnesium stearate, malt, mannitol, monoglycerides, olive oil, peanut oil, potassium phosphate salts, potato starch, povidone, propylene glycol, Ringer's solution, safflower oil, sesame oil, sodium carboxymethyl cellulose, sodium phosphate salts, sodium lauryl sulfate, sodium sorbitol, soybean oil, stearic acids, stearyl fumarate, sucrose, surfactants, talc, tragacanth, tetrahydrofurfuryl alcohol, triglycerides, water, mixtures thereof and the like. Excipients for preparation of compositions comprising a compound having formula (I) to be administered ophthalmically or orally include, but are not limited to, 1,3-butylene glycol, castor oil, corn oil, cottonseed oil, ethanol, fatty acid esters of sorbitan, germ oil, groundnut oil, glycerol, isopropanol, olive oil, polyethylene glycols, propylene glycol, sesame oil, water, mixtures thereof and the like. Excipients for preparation of compositions comprising a compound having formula (I) to be administered osmotically include, but are not limited to, chlorofluorohydrocarbons, ethanol, water, mixtures thereof and the like. Excipients for preparation of compositions comprising a compound having formula (I) to be administered parenterally include, but are not limited to, 1,3-butanediol, castor oil, corn oil, cottonseed oil, dextrose, germ oil, groundnut oil, liposomes, oleic acid, olive oil, peanut oil, Ringer's solution, safflower oil, sesame oil, soybean oil, U.S.P. or isotonic sodium chloride solution, water, mixtures thereof and the like. Excipients for preparation of compositions comprising a compound having formula (I) to be administered rectally or vaginally include, but are not limited to, cocoa butter, polyethylene glycol, wax, mixtures thereof and the like.
Compounds having formula (I) are also expected to be useful when used with alkylating agents, angiogenesis inhibitors, antibodies, antimetabolites, antimitotics, antiproliferatives, aurora kinase inhibitors, Bcr-Abl kinase inhibitors, biologic response modifiers, cyclin-dependent kinase inhibitors, cell cycle inhibitors, cyclooxygenase-2 inhibitors, leukemia viral oncogene homolog (ErbB2) receptor inhibitors, growth factor inhibitors, heat shock protein (HSP)-90 inhibitors, histone deacetylase (HDAC) inhibitors inhibitors, hormonal therapies, immunologicals, intercalating antibiotics, kinase inhibitors, mammalian target of rapomycin inhibitors, mitogen-activated extracellular signal-regulated kinase inhibitors, non-steroidal anti-inflammatory drugs (NSAID's), platinum chemotherapeutics, polo-like kinase inhibitors, proteasome inhibitors, purine analogs, pyrimidine analogs, receptor tyrosine kinase inhibitors, retinoids/deltoids plant alkaloids, topoisomerase inhibitors and the like.
Alkylating agents include altretamine, AMD-473, AP-5280, apaziquone, bendamustine, brostallicin, busulfan, carboquone, carmustine (BCNU), chlorambucil, Cloretazine™ (VNP 40101M), cyclophosphamide, decarbazine, estramustine, fotemustine, glufosfamide, ifosfamide, KW-2170, lomustine (CCNU), mafosfamide, melphalan, mitobronitol, mitolactol, nimustine, nitrogen mustard N-oxide, ranimustine, temozolomide, thiotepa, treosulfan, trofosfamide and the like.
Angiogenesis inhibitors include endothelial-specific receptor tyrosine kinase (Tie-2) inhibitors, epidermal growth factor receptor (EGFR) inhibitors, insulin growth factor-2 receptor (IGFR-2) inhibitors, matrix metalloproteinase-2 (MMP-2) inhibitors, matrix metalloproteinase-9 (MMP-9) inhibitors, platelet-derived growth factor receptor (PDGFR) inhibitors, thrombospondin analogs vascular endothelial growth factor receptor tyrosine kinase (VEGFR) inhibitors and the like.
Aurora kinase inhibitors include AZD-1152, MLN-8054, VX-680 and the like.
Bcr-Abl kinase inhibitors include DASATINIB® (BMS-354825), GLEEVEC® (imatinib) and the like.
CDK inhibitors include AZD-5438, BMI-1040, BMS-032, BMS-387, CVT-2584, flavopyridol, GPC-286199, MCS-5A, PD0332991, PHA-690509, seliciclib (CYC-202, R-roscovitine), ZK-304709 and the like.
COX-2 inhibitors include ABT-963, ARCOXIA® (etoricoxib), BEXTRA® (valdecoxib), BMS347070, CELEBREX™ (celecoxib), COX-189 (lumiracoxib), CT-3, DERAMAXX® (deracoxib), JTE-522, 4-methyl-2-(3,4-dimethylphenyl)-1-(4-sulfamoylphenyl-1H-pyrrole), MK-663 (etoricoxib), NS-398, parecoxib, RS-57067, SC-58125, SD-8381, SVT-2016, S-2474, T-614, VIOXX® (rofecoxib) and the like.
EGFR inhibitors include ABX-EGF, anti-EGFr immunoliposomes, EGF-vaccine, EMD-7200, ERBITUX® (cetuximab), HR3, IgA antibodies, IRESSA® (gefitinib), TARCEVA® (erlotinib or OSI-774), TP-38, EGFR fusion protein, TYKERB® (lapatinib) and the like.
ErbB2 receptor inhibitors include CP-724-714, CI-1033 (canertinib), Herceptin® (trastuzumab), TYKERB® (lapatinib), OMNITARG® (2C4, petuzumab), TAK-165, GW-572016 (ionafarnib), GW-282974, EKB-569, PI-166, dHER2 (HER2 vaccine), APC-8024 (HER-2 vaccine), anti-HER/2neu bispecific antibody, B7.her2IgG3, AS HER2 trifunctional bispecfic antibodies, mAB AR-209, mAB 2B-1 and the like.
Histone deacetylase inhibitors include depsipeptide, LAQ-824, MS-275, trapoxin, suberoylanilide hydroxamic acid (SAHA), TSA, valproic acid and the like.
HSP-90 inhibitors include 17-AAG-nab, 17-AAG, CNF-101, CNF-1010, CNF-2024. 17-DMAG, geldanamycin, IPI-504, KOS-953, MYCOGRAB®, NCS-683664, PU24FCl, PU-3, radicicol, SNX-2112, STA-9090 VER49009 and the like.
MEK inhibitors include ARRY-142886, ARRY-438162 PD-325901, PD-98059 and the like.
mTOR inhibitors include AP-23573, CCI-779, everolimus, RAD-001, rapamycin, temsirolimus and the like.
Non-steroidal anti-inflammatory drugs include AMIGESIC® (salsalate), DOLOBID® (diflunisal), MOTRIN® (ibuprofen), ORUDIS® (ketoprofen), RELAFEN® (nabumetone), FELDENE® (piroxicam) ibuprofin cream, ALEVE® and NAPROSYN® (naproxen), VOLTAREN® (diclofenac), INDOCIN® (indomethacin), CLINORIL® (sulindac), TOLECTIN® (tolmetin), LODINE® (etodolac), TORADOL® (ketorolac), DAYPRO® (oxaprozin) and the like.
PDGFR inhibitors include C-451, CP-673, CP-868596 and the like.
Platinum chemotherapeutics include cisplatin, ELOXATIN® (oxaliplatin) eptaplatin, lobaplatin, nedaplatin, PARAPLATIN® (carboplatin), satraplatin and the like.
Polo-like kinase inhibitors include BI-2536 and the like.
Thrombospondin analogs include ABT-510, ABT-567, ABT-898, TSP-1 and the like.
VEGFR inhibitors include AVASTIN® (bevacizumab), ABT-869, AEE-788, ANGIOZYME™, axitinib (AG-13736), AZD-2171, CP-547,632, IM-862, Macugen (pegaptamib), NEXAVAR® (sorafenib, BAY43-9006), pazopanib (GW-786034), (PTK-787, ZK-222584), SUTENT® (sunitinib, SU-11248), VEGF trap, vatalanib, ZACTIMA™ (vandetanib, ZD-6474) and the like.
Antimetabolites include ALIMTA® (premetrexed disodium, LY231514, MTA), 5-azacitidine, XELODA® (capecitabine), carmofur, LEUSTAT® (cladribine), clofarabine, cytarabine, cytarabine ocfosfate, cytosine arabinoside, decitabine, deferoxamine, doxifluridine, eflomithine, EICAR, enocitabine, ethnylcytidine, fludarabine, hydroxyurea, 5-fluorouracil (5-FU) alone or in combination with leucovorin, GEMZAR® (gemcitabine), hydroxyurea, ALKERAN® (melphalan), mercaptopurine, 6-mercaptopurine riboside, methotrexate, mycophenolic acid, nelarabine, nolatrexed, ocfosate, pelitrexol, pentostatin, raltitrexed, Ribavirin, triapine, trimetrexate, S-1, tiazofurin, tegafur, TS-1, vidarabine, UFT and the like.
Antibiotics include intercalating antibiotics aclarubicin, actinomycin D, amrubicin, annamycin, adriamycin, BLENOXANE® (bleomycin), daunorubicin, CAELYX® or MYOCET® (doxorubicin), elsamitrucin, epirbucin, glarbuicin, ZAVEDOS® (idarubicin), mitomycin C, nemorubicin, neocarzinostatin, peplomycin, pirarubicin, rebeccamycin, stimalamer, streptozocin, VALSTAR® (valrubicin), zinostatin and the like.
Topoisomerase inhibitors include aclarubicin, 9-aminocamptothecin, amonafide, amsacrine, becatecarin, belotecan, BN-80915, CAMPTOSAR® (irinotecan hydrochloride), camptothecin, CARDIOXANE® (dexrazoxine), diflomotecan, edotecarin, ELLENCE® or PHARMORUBICIN® (epirubicin), etoposide, exatecan, 10-hydroxycamptothecin, gimatecan, lurtotecan, mitoxantrone, orathecin, pirarbucin, pixantrone, rubitecan, sobuzoxane, SN-38, tafluposide, topotecan and the like.
Antibodies include AVASTIN® (bevacizumab), CD40-specific antibodies, chTNT-1/B, denosumab, ERBITUX® (cetuximab), HUMAX-CD4® (zanolimumab), IGF1R-specific antibodies, lintuzumab, PANOREX® (edrecolomab), RENCAREX® (WX G250), RITUXAN® (rituximab), ticilimumab, trastuzimab and and the like.
Hormonal therapies include ARIMIDEX® (anastrozole), AROMASIN® (exemestane), arzoxifene, CASODEX® (bicalutamide), CETROTIDE® (cetrorelix), degarelix, deslorelin, DESOPAN® (trilostane), dexamethasone, DROGENIL®, (flutamide), EVISTA® (raloxifene), fadrozole, FARESTON® (toremifene), FASLODEX® (fulvestrant), FEMARA®, (letrozole), formestane, glucocorticoids, HECTOROL® or RENAGEL® (doxercalciferol), lasofoxifene, leuprolide acetate, MEGACE® (megesterol), MIFEPREX® (mifepristone), NILANDRON™ (nilutamide), NOLVADEX® (tamoxifen citrate), PLENAXIS™ (abarelix), predisone, PROPECIA® (finasteride), rilostane, SUPREFACT® (buserelin), TRELSTAR® (luteinizing hormone releasing hormone (LHRH)), vantas, VETORYL®, (trilostane or modrastane), ZOLADEX® (fosrelin, goserelin) and the like.
Deltoids and retinoids include seocalcitol (EB1089, CB1093), lexacalcitrol (KH1060), fenretinide, PANRETIN® (aliretinoin), ATRAGEN® (liposomal tretinoin), TARGRETIN® (bexarotene), LGD-1550 and the like.
Plant alkaloids include, but are not limited to, vincristine, vinblastine, vindesine, vinorelbine and the like.
Proteasome inhibitors include VELCADE® (bortezomib), mg132, NPI-0052, PR-171 and the like.
Examples of immunologicals include interferons and other immune-enhancing agents. Interferons include interferon alpha, interferon alpha-2a, interferon alpha-2b, interferon beta, interferon gamma-1a, ACTIMMUNE® (interferon gamma-1b), or interferon gamma-n1, combinations thereof and the like. Other agents include ALFAFERONE®, BAM-002, BEROMUN® (tasonermin), BEXXAR® (tositumomab), CamPath® (alemtuzumab), CTLA4 (cytotoxic lymphocyte antigen 4), decarbazine, denileukin, epratuzumab, GRANOCYTE® (lenograstim), lentinan, leukocyte alpha interferon, imiquimod, MDX-010, melanoma vaccine, mitumomab, molgramostim, MYLOTARGTM (gemtuzumab ozognamicin), NEUPOGEN® (filgrastim), OncoVAC-CL, OvaRex® (oregovomab), pemtumomab (Y-muHMFG1), PROVENGE®, sargaramostim, sizofilan, teceleukin, TheraCys®, ubenimex, VIRULIZIN®, Z-F100, WF-10, PROLEUKIN®, (aldesleukin), ZADAXIN® (thymalfasin), ZENAPAX® (daclizumab), ZEVALIN® (90Y-Ibritumomab tiuxetan) and the like.
Biological response modifiers are agents that modify defense mechanisms of living organisms or biological responses, such as survival, growth, or differentiation of tissue cells to direct them to have anti-tumor activity and include include krestin, lentinan, sizofiran, picibanil PF-3512676 (CpG-8954), ubenimex and the like.
Pyrimidine analogs include cytarabine (ara C), cytosine arabinoside, doxifluridine, FLUDARA® (fludarabine), 5-FU (5-fluorouracil), floxuridine, GEMZAR® (gemcitabine), TOMUDEX® (ratitrexed), TROXATYL™ (triacetyluridine troxacitabine) and the like.
Purine analogs include LANVIS® (thioguanine) and PURI-NETHOL® (mercaptopurine).
Antimitotic agents include batabulin, epothilone D (KOS-862), N-(2-((4-hydroxyphenyl)amino)pyridin-3-yl)-4-methoxybenzenesulfonamide, ixabepilone (BMS 247550), paclitaxel, TAXOTERE® (docetaxel), PNU100940 (109881), patupilone, XRP-9881, vinflunine, ZK-EPO and the like.
Compounds of the present invention are also intended to be used as a radiosensitizer that enhances the efficacy of radiotherapy. Examples of radiotherapy include, but are not limited to, external beam radiotherapy, teletherapy, brachtherapy and sealed and unsealed source radiotherapy.
Additionally, compounds having formula (I) may be combined with other chemptherapeutic agents such as ABRAXANE™ (ABI-007), ABT-100 (famesyl transferase inhibitor), ADVEXIN®, ALTOCOR® or MEVACOR® (lovastatin), AMPLIGEN® (poly I:poly C12U, a synthetic RNA), APTOSYN™ (exisulind), AREDIA® (pamidronic acid), arglabin, L-asparaginase, atamestane (1-methyl-3,17-dione-androsta-1,4-diene), AVAGE® (tazarotne), AVE-8062, BEC2 (mitumomab), cachectin or cachexin (tumor necrosis factor), canvaxin (vaccine), CeaVac™ (cancer vaccine), CELEUK® (celmoleukin), CEPLENE® (histamine dihydrochloride), CERVARIX™ (human papillomavirus vaccine), CHOP® (C: CYTOXAN® (cyclophosphamide); H: ADRIAMYCIN® (hydroxydoxorubicin); O: Vincristine (ONCOVIN®); P: prednisone), CyPat™, combrestatin A4P, DAB(389)EGF or TransMID-107R™ (diphtheria toxins), dacarbazine, dactinomycin, 5,6-dimethylxanthenone-4-acetic acid (DMXAA), eniluracil, EVIZON™ (squalamine lactate), DIMERICINE®0 (T4N5 liposome lotion), discodermolide, DX-895 If (exatecan mesylate), enzastaurin, EPO906, GARDASIL® (quadrivalent human papillomavirus (Types 6, 11, 16, 18) recombinant vaccine), gastrimmune, genasense, GMK (ganglioside conjugate vaccine), GVAX® (prostate cancer vaccine), halofuginone, histerelin, hydroxycarbamide, ibandronic acid, IGN-101, IL-13-PE38, IL-13-PE38QQR (cintredekin besudotox), IL-13-pseudomonas exotoxin, interferon-α, interferon-γ, JUNOVAN™ or MEPACT™ (mifamurtide), lonafarnib, 5,10-methylenetetrahydrofolate, miltefosine (hexadecylphosphocholine), NEOVASTAT®9(AE-941), NEUTREXIN® (trimetrexate glucuronate), NIPENT® (pentostatin), ONCONASE® (a ribonuclease enzyme), ONCOPHAGE® (melanoma vaccine treatment), OncoVAX (IL-2 Vaccine), ORATHECIN™ (rubitecan), OSIDEM® (antibody-based cell drug), OvaRex® MAb (murine monoclonal antibody), paditaxel, PANDIMEX™ (aglycone saponins from ginseng comprising 20(S)protopanaxadiol (aPPD) and 20(S)protopanaxatriol (aPPT)), panitumumab, PANVAC®-VF. (investigational cancer vaccine), pegaspargase, PEG Interferon A, phenoxodiol, procarbazine, rebimastat, REMOVAB® (catumaxomab), REVLIMID® (lenalidomide), RSR13 (efaproxiral), SOMATULINE® LA (lanreotide), SORIATANE® (acitretin), staurosporine (Streptomyces staurospores), talabostat (PT100), TARGRETIN® (bexarotene), Taxoprexin® (DHA-paclitaxel), TELCYTA™ (TLK286), temilifene, TEMODAR® (temozolomide), tesmilifene, thalidomide, THERATOPE® (STn-KLH), thymitaq (2-amino-3,4-dihydro-6-methyl-4-oxo-5-(4-pyridylthio)quinazoline dihydrochloride), TNFerade™ (adenovector: DNA carrier containing the gene for tumor necrosis factor-α), TRACLEER® or ZAVESCA® (bosentan), tretinoin (Retin-A), tetrandrine, TRISENOX® (arsenic trioxide), VIRULIZIN®, ukrain (derivative of alkaloids from the greater celandine plant), vitaxin (anti-alphavbeta3 antibody), XCYTRIN® (motexafin gadolinium), XINLAY™ (atrasentan), XYOTAX™ (paclitaxel poliglumex), YONDELIS™ (trabectedin), ZD-6126, ZINECARD® (dexrazoxane), zometa (zolendronic acid), zorubicin and the like.
To determine the inhibitory activity of representative compounds having formula (I) to protein kinases, the following assay was used:
In 384-well v-bottom polypropylene plates (Axygen #P-384-120SQ C), 10 μL recombinant Aurora Kinase-A (AurA, Upstate #14-511, 1 nM final concentration) was mixed with 10 μL biotinylated peptide substrate (Genemed, 2 μM final concentration), and various concentrations of representative compounds (2% DMSO final) in reaction buffer (25 mM HEPES, pH 7.5, 0.5 mM DTT, 10 mM mgCl2 100 μM Na3VO4, 0.075 mg/mL Triton X-100). The reaction was initiated by adding [33P]-ATP (Perkin Elmer, 5 μM final concentration, 2 mCi/umol,). The reaction was quenched after 1 hour by addition of 50 μl stop buffer (50 mM EDTA, 2M NaCl final concentration). 80 μL of the stopped reactions were transferred to 384-well streptavidin-coated FlashPlates (Perkin Elmer, #SMP410A0001PK), incubated 10 minutes at ambient temperature, washed 3 times with 0.05% Tween-20/PBS using an ELX-405 automated plate washer (BioTek) and counted on a TopCount Scintillation Plate Reader (Packard).
IC50 values values are shown in TABLE 1.
These data demonstrate the utility of compounds having formula (I) as inhibitors of Aurora-kinase A.
To determine the activity of other representative compounds of the invention, Active Aurora A enzyme was incubated in wells of a 384 well plate with biotinylated STK substrate-2 (Upstate), 1 mM ATP, and various concentrations of inhibitors in a Hepes buffer, pH 7.4 containing MgCl2, sodium othrovanadate, and Triton X-100. After 1 hour, the reaction was stopped with EDTA and anti-phospho-STK antibody Europium Cryptate (Upstate) and SA-XL665 (Upstate) were added to detect the phosphopeptide. The amount of phosphorylation was determined by the time-resolved fluorescence ratio of signals at 665 nm and 615 nm. The IC50's were calculated by an exponential fit of the inhibition values with the inhibitor concentrations using Assay Explorer software.
It is expected that, because compounds having formula (I) inhibit the activity of Aurora-kinase A, they could also have utility as inhibitors of protein kinases having close structural homology to Aurora-kinase A such as, for example, Aurora-kinase B and Aurora-kinase C.
The structural homology between protein kinases A, B and C is reported in Nature Reviews/Cancer, Vol. 4 December, 2004.
Accordingly, compounds having formula (I) are expected to have utility in treatment of diseases during which protein kinases such as any or all Aurora-kinase family members are expressed.
Diseases involving overexpression or unregulation of Aurora-kinase family members include, but are not limited to, acoustic neuroma, acute leukemia, acute lymphocytic leukemia, acute myelocytic leukemia (monocytic, myeloblastic, adenocarcinoma, angiosarcoma, astrocytoma, myelomonocytic and promyelocytic), acute t-cell leukemia, basal cell carcinoma, bile duct carcinoma, bladder cancer, brain cancer, breast cancer, bronchogenic carcinoma, cervical cancer, chondrosarcoma, chordoma, choriocarcinoma, chronic leukemia, chronic lymphocytic leukemia, chronic myelocytic (granulocytic) leukemia, chronic myleogeneous leukemia, colon cancer, colorectal cancer, craniopharyngioma, cystadenocarcinoma, diffuse large B-cell lymphoma, dysproliferative changes (dysplasias and metaplasias), embryonal carcinoma, endometrial cancer, endotheliosarcoma, ependymoma, epithelial carcinoma, erythroleukemia, esophageal cancer, estrogen-receptor positive breast cancer, essential thrombocythemia, Ewing's tumor, fibrosarcoma, follicular lymphoma, germ cell testicular cancer, glioma, heavy chain disease, hemangioblastoma, hematological cancers (leukemias such as acute lymphocytic leukemia, chronic lymphocytic leukemia and chronic myeloid leukemia) and lymphomas), hepatoma, hepatocellular cancer, hormone insensitive prostate cancer, leiomyosarcoma, liposarcoma, lung cancer, lymphagioendotheliosarcoma, lymphangiosarcoma, lymphoblastic leukemia, lymphoma (Hodgkin's and non-Hodgkin's), malignancies and hyperproliferative disorders of the bladder, breast, colon, lung, ovaries, pancreas, prostate, skin and uterus, lymphoid malignancies of T-cell or B-cell origin, leukemia, lymphoma, medullary carcinoma, medulloblastoma, melanoma, meningioma, mesothelioma, multiple myeloma, myelogenous leukemia, myeloma, myxosarcoma, neuroblastoma, non-small cell lung cancer, oligodendroglioma, oral cancer, osteogenic sarcoma, ovarian cancer, pancreatic cancer, papillary adenocarcinomas, papillary carcinoma, pinealoma, polycythemia vera, prostate cancer, rectal cancer, renal cell carcinoma, retinoblastoma, rhabdomyosarcoma, sarcoma, sebaceous gland carcinoma, seminoma, skin cancer, small cell lung carcinoma, solid tumors (carcinomas and sarcomas), small cell lung cancer, stomach cancer, squamous cell carcinoma, synovioma, sweat gland carcinoma, thyroid cancer, Waldenstrom's macroglobulinemia, testicular tumors, uterine cancer and Wilms' tumor.
It is also expected that compounds having formula (I) would inhibit the growth of cells derived from a cancer or neoplasm such as breast cancer (including estrogen-receptor positive breast cancer), colorectal cancer, endometrial cancer, lung cancer (including small cell lung cancer), lymphoma (including follicular or Diffuse Large B-cell), lymphoma (including non-Hodgkin's Iymphoma), neuroblastoma, ovarian cancer, prostate cancer (including hormone-insensitive prostate cancer) and testicular cancer (including germ cell testicular cancer).
It is also expected that compounds having formula (I) would inhibit the growth of cells derived from a pediatric cancer or neoplasm such as embryonal rhabdomyosarcoma, pediatric acute lymphoblastic leukemia, pediatric acute myelogenous leukemia, pediatric alveolar rhabdomyosarcoma, pediatric anaplastic ependymoma, pediatric anaplastic large cell lymphoma, pediatric anaplastic medulloblastoma, pediatric atypical teratoid/rhabdoid tumor of the central nervous syatem, pediatric biphenotypic acute leukemia, pediatric Burkitts lymphoma, pediatric cancers of Ewing's family of tumors such as primitive neuroectodermal rumors, pediatric diffuse anaplastic Wilm's tumor, pediatric favorable histology Wilm's tumor, pediatric glioblastoma, pediatric medulloblastoma, pediatric neuroblastoma, pediatric neuroblastoma-derived myelocytomatosis, pediatric pre-B-cell cancers (such as leukemia), pediatric psteosarcoma, pediatric rhabdoid kidney tumor, pediatric rhabdomyosarcoma, and pediatric T-cell cancers such as lymphoma and skin cancer.
For example, involvement of Aurora-kinases in bladder cancer, breast cancer, cervical cancer, colon cancer, endometrial cancer, esophageal cancer, lung cancer, ovarian cancer, pancreatic cancer, prostate cancer, rectal cancer, skin cancer, stomach cancer and thyroid cancer is reported in Nature Reviews/Cancer, Vol. 4 December, 2004.
Compounds having formula (I) may be made by synthetic chemical processes, examples of which are shown hereinbelow. It is meant to be understood that the order of the steps in the processes may be varied, that reagents, solvents and reaction conditions may be substituted for those specifically mentioned, and that vulnerable moieties may be protected and deprotected, as necessary.
Protecting groups for C(O)OH moieties include, but are not limited to, acetoxymethyl, allyl, benzoylmethyl, benzyl, benzyloxymethyl, tert-butyl, tert-butyldiphenylsilyl, diphenylmethyl, cyclobutyl, cyclohexyl, cyclopentyl, cyclopropyl, diphenylmethylsilyl, ethyl, para-methoxybenzyl, methoxymethyl, methoxyethoxymethyl, methyl, methylthiomethyl, naphthyl, para-nitrobenzyl, phenyl, n-propyl, 2,2,2-trichloroethyl, triethylsilyl, 2-(trimethylsilyl)ethyl, 2-(trimethylsilyl)ethoxymethyl, triphenylmethyl and the like.
Protecting groups for C(O) and C(O)H moieties include, but are not limited to, 1,3-dioxylketal, diethylketal, dimethylketal, 1,3-dithianylketal, O-methyloxime, O-phenyloxime and the like.
Protecting groups for NH moieties include, but are not limited to, acetyl, alanyl, benzoyl, benzyl(phenylmethyl), benzylidene, benzyloxycarbonyl (Cbz), tert-butoxycarbonyl (Boc), 3,4-dimethoxybenzyloxycarbonyl, diphenylmethyl, diphenylphosphoryl, formyl, niethanesulfonyl, para-methoxybenzyloxycarbonyl, phenylacetyl, phthaloyl, succinyl, trichloroethoxycarbonyl, triethylsilyl, trifluoroacetyl, trimethylsilyl, triphenylmethyl, triphenylsilyl, para-toluenesulfonyl and the like.
Protecting groups for OH and SH moieties include, but are not limited to, acetyl, allyl, allyloxycarbonyl, benzyloxycarbonyl (Cbz), benzoyl, benzyl, tert-butyl, tert-butyldimethylsilyl, tert-butyldiphenylsilyl, 3,4-dimethoxybenzyl, 3,4-dimethoxybenzyloxycarbonyl, 1,1-dimethyl-2-propenyl, diphenylmethyl, formyl, methanesulfonyl, methoxyacetyl, 4-methoxybenzyloxycarbonyl, para-methoxybenzyl, methoxycarbonyl, methyl, para-toluenesulfonyl, 2,2,2-trichloroethoxycarbonyl, 2,2,2-trichloroethyl, triethylsilyl, trifluoroacetyl, 2-(trimethylsilyl)ethoxycarbonyl, 2-trimethylsilylethyl, triphenylmethyl, 2-(triphenylphosphonio)ethoxycarbonyl and the like.
The following abbreviations have the meanings indicated. ADDP means 1,1′-(azodicarbonyl)dipiperidine; AD-mix-β means a mixture of (DHQD)2PHAL, K3Fe(CN)6, K2CO3 and K2SO4); AIBN means 2,2′-azobis(2-methylpropionitrile); 9-BBN means 9-borabicyclo[3.3.1]nonane; Cp means cyclopentadiene; (DHQD)2PHAL means hydroquinidine 1,4-phthalazinediyl diethyl ether; DBU means 1,8-diazabicyclo[5.4.0]undec-7-ene; DIBAL means diisobutylaluminum hydride; DIEA means diisopropylethylamine; DMAP means N,N-dimethylaminopyridine; DME means 1,2-dimethoxyethane; DMF means N,N-dimethylformamide; dmpe means 1,2-bis(dimethylphosphino)ethane; DMSO means dimethylsulfoxide; dppa means diphenylphosphoryl azide; dppb means 1,4-bis(diphenylphosphino)butane; dppe means 1,2-bis(diphenylphosphino)ethane; dppf means 1,1′-bis(diphenylphosphino)ferrocene; dppm means 1,1-bis(diphenylphosphino)methane; EDAC means 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide; Fmoc means fluorenylmethoxycarbonyl; HATU means O-(7-azabenzotriazol-1-yl)-N,N′N′N′-tetramethyluronium hexafluorophosphate; HMPA means hexamethylphosphoramide; IPA means isopropyl alcohol; LDA means lithium diisopropylamide; LHMDS means lithium bis(hexamethyldisilylamide); MP—BH3 means macroporus triethylammonium methylpolystyrene cyanoborohydride; LAH means lithium aluminum hydride; NCS means N-chlorosuccinimide; PyBOP means benzotriazol-1-yloxytripyrrolidinophosphonium hexafluorophosphate; TDA-1 means tris(2-(2-methoxyethoxy)ethyl)amine; TEA means triethylamine; TFA means trifluoroacetic acid; THF means tetrahydrofuran; NCS means N-chlorosuccinimide; NMM means N-methylmorpholine; NMP means N-methylpyrrolidine; and PPh3 means triphenylphosphine.
Compounds having formula (1) can be described herein and converted to compounds having formula (2) by the former and DPPA followed by hydrolysis of the product with water. The reactions are typically conducted in solvents such as benzene, toluene, THF, mixtures thereof and the like at temperatures between about 50° C. and 110° C.
Introduction of moieties represented by A1 can be accomplished by reacting the compounds having formula (1), a compound having formula H2NR1 or HN(R1)2, a coupling agent and a base, with or without DMAP. Examples of coupling agents include DCC, EDCI and the like. Examples of bases include TEA, DIEA, pyridine and the like. The reactions are typically conducted in solvents such as THF, dichloromethane, DMF, DMSO, chloroform, mixtures thereof and the like at temperatures between about 0° C. and 25° C.
Introduction of moieties represented by A1 can also be accomplished by reacting the compounds having formula (2) and the appropriate isocyanate, carbonyl chloride, sulfonyl chloride, carbamoyl chloride. The reactions are typically conducted in solvents such as THF, ethyl acetate, dichloromethane, DMF, DMSO, chloroform, mixtures thereof and the like at temperatures between about 0° C. and 110° C., depending on the reactivity of the starting materials.
The following examples are presented to provide what is believed to be the most useful and readily understood description of procedures and conceptual aspects of this invention.
A mixture of 5-amino-4-cyano-thiophene-3-carboxylic acid ethyl ester (2.4 g, prepared as described in Annali. di Chimica, 64, 833, 1974) in formamide (45 mL) at 170° C. was stirred for 8 hours and concentrated. The concentrate was flash chromatographed on silica gel with 10-50% ethyl acetate/hexanes.
A mixture of EXAMPLE 1A (0.62 g) and LiOH.H2O (0.54 g) in THF (54 mL), water (13 mL) and methanol (13 mL) at 80° C. was stirred for 16 hours, cooled to ambient temperature and concentrated. The concentrate was taken up in water, cooled in an ice bath, stirred for 30 minutes and treated with 1N HCl until acidic, stirred for 30 minutes and filtered.
A mixture of 1-isocyanato-3-methylbenzene (0.6 mL) was added to a mixture of (4-aminophenyl)carbamic acid tert-butyl ester (1 g) in dichloromethane (48 mL) 0° C. The mixture was stirred for 30 minutes, warmed to ambient temperature, stirred for 24 hours and filtered. The filtrant was suspended in dichloromethane (80 mL), cooled in an ice bath, treated with TFA (5 mL), stirred for 15 minutes, warmed to ambient temperature, stirred for 18 hours and concentrated. The concentrate was concentrated twice from methanol and toluene.
Diisopropylethyl amine (0.3 mL) was added to a mixture of EXAMPLE 1B (0.2 g), EXAMPLE 1C (0.336 g) and HATU (0.452 g) in DMF (5.7 mL) at 0° C. The mixture was stirred for 0.5 hours, warmed to ambient temperature, stirred for for 20 hours, cooled to 0° C., diluted with water (80 mL), stirred for 1 hour and filtered. The filtrant was washed with water, dried and triturated with 2:1 dichloromethane/methanol. 1H NMR (400 MHz, DMSO-d6) δ 10.63 (s, 1H), 8.66 (s, 1H), 8.55 (s, 1H), 8.37 (s, 1H), 8.32 (s, 1H), 7.98 (br s, 2H), 7.63 (d, 2H), 7.46 (d, 2H), 7.30 (s, 1H), 7.18 (m, 2H), 6.79 (d, 1H), 2.28 (s, 3H).
This example was prepared by substituting 1-fluoro-3-isocyanatobenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (500 MHz, DMSO-d6) δ 10.67 (s, 1H), 8.89 (s, 1H), 8.76 (s, 1H), 8.37 (s, 1H), 8.32 (s, 1H), 8.02 (brs, 2H), 7.64 (d, 2H), 7.51 (s, 1H),7.47 (d, 2H), 7.30 (m, 1H), 7.12 (d, 1H), 6.78 (m, 1H).
This example was prepared by substituting 1-fluoro-3-isocyanato-4-methylbenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (500 MHz, DMSO-d6) δ 10.67 (s, 1H), 8.76 (s, 1H), 8.72 (s, 1H), 8.39 (s, 1H), 8.34 (s, 1H), 7.93 (s, 2H), 7.64 (d, 2H), 7.45 (m, 3H), 7.16 (m, 1H), 7.03 (d, 1H), 2.17 (s, 3H).
This example was prepared by substituting 1-isocyanato-4-methylbenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (400 MHz, DMSO-d6) δ 10.63 (d, 1H), 8.62 (d, 1H), 8.51 (d, 1H), 8.37 (d, 1H) 8.32 (d, 1H), 8.00 (brs, 2H), 7.62 (d, 2H), 7.46 (d, 2H), 7.33 (d, 2H), 7.08 (d, 2H), 2.24 (m, 3H).
This example was prepared by substituting 1-fluoro-4-isocyanatobenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (500 MHz, DMSO-d6) δ 10.66 (s, 1H), 8.68 (s, 2H), 8.37 (s, 1H), 8.32 (s, 1H), 7.92 (brs, 2H), 7.63 (d, 2H), 7.47 (d, 4H), 7.12 (t, 2H).
This example was prepared by substituting 1-chloro-2-fluoro-4-isocyanatobenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (500 MHz, DMSO-d6) δ 10.67 (s, 1H), 8.86 (s, 1H), 8.79 (s, 1H), 8.38 (s, 1H), 8.33 (s, 1H), 8.07 (brs, 2H), 7.81 (d, 1H), 7.64 (d, 2H), 7.47 (d, 2H), 7.32 (m, 2H).
This example was prepared by substituting 1-ethyl-3-isocyanatobenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (300 MHz, DMSO-d6) δ 10.64 (s, 1H), 8.65 (s, 1H), 8.57 (s, 1H), 8.38 (s, 1H), 8.33 (s, 1H), 7.63 (d, 2H), 7.46 (d, 2H), 7.24 (m, 5H), 6.82 (d, 1H), 2.58 (m, 2H), 1.18 (t, 3H).
This example was prepared by substituting 1-chloro-3-isocyanatobenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (500 MHz, DMSO-d6) δ 10.67 (s, 1H), 8.87 (s, 1H), 8.78 (s, 1H), 8.38 (s. 1H). 8.32 (s, 1H), 7.72 (s, 1H), 7.64 (d, 2H), 7.68 (brs, 2H), 7.47 (d, 2H), 7.28 (m, 2H), 7.02 (d, 1H).
This example was prepared by substituting 1-cyano-3-isocyanatobenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (300 MHz, DMSO-d6) δ 10.67 (s, 1H), 9.00 (s, 1H), 8.86 (s, 1H), 8.37 (s, 1H), 8.32 (s, 1H), 7.98 (m, 1H), 7.99 (brs, 2H), 7.66 (m, 3H), 7.46 (m, 4H).
This example was prepared by substituting 1-fluoro-2-isocyanatobenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (500 MHz, DMSO-d6) δ 10.68 (s, 1H), 9.11 (s, 1H), 8.54 (s, 1H), 8.38 (s, 1H), 8.32 (s, 1H), 8.16 (t, 1H), 7.83 (brs, 2H), 7.66 (d, ,2H), 7.48 (d, 2H), 7.24 (m, 1H), 7.14 (t, 1H), 7.01 (m, 1H).
This example was prepared by substituting 1-isocyanato-3-trifluoromethylbenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (300 MHz, DMSO-d6) δ 10.67 (s, 1H), 9.02 (s, 1H), 8.81 (s, 1H), 8.38 (s, 1H), 8.32 (s, 1H), 8.03 (s, 1H), 8.00 (brs, 2H), 7.65 (d, 2H), 7.56 (m, 2H), 7.48 (d, 2H), 7.31 (d, 1H).
This example was prepared by substituting 1-fluoro-4-isocyanato-2-trifluoromethylbenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (300 MHz, DMSO-d6) δ 10.67 (s, 1H), 9.01 (s, 1H), 8.83 (s, 1H), 8.38 (s, 1H), 8.32 (s, 1H), 8.02 (dd, 2H), 7.98 (brs, 2H), 7.65 (d, 2H), 7.46 (m, 3H).
This example was prepared by substituting 1-isocyanato-3-methoxybenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (400 MHz, DMSO-d6) δ 10.64 (s, 1H), 8.66 (s, 1H), 8.64 (s, 1H), 8.38 (s, 1H), 8.32 (s, 1H), 8.02 (brs, 2H), 7.63 (d, 2H), 7.47 (d, 2H), 7.19 (s, 1H), 7.16 (d, 1H), 6.93 (d, 1H), 6.55 (d, 1H), 3.74 (s, 3H).
This example was prepared by substituting 1-fluoro-3-isocyanato-4-methylbenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (400 MHz, DMSO-d6) δ 10.66 (s, 1H), 9.19 (s, 1H), 8.38 (s, 1H), 8.32 (s, 1H), 8.02 (s, 3H), 7.86 (dd, 1H), 7.66 (d, 2H), 7.49 (d, 2H), 7.19 (t, 1H), 6.74 (m, 1H), 2.23 (s, 3H).
This example was prepared by substituting 1-isocyanato-4-trifluoromethylbenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (500 MHz, DMSO-d6) δ 10.69 (s, 1H), 9.09 (s, 1H) 8.39 (s, 1H), 8.39 (s, 1H), 8.34 (s, 1H), 7.88 (brs, 2H), 7.65 (, 6H), 7.49 (d, 2H).
This example was prepared by substituting 1-fluoro-2-isocyanato-4-methylbenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (500 MHz, DMSO-d6) δ 10.67 (s, 1H), 9.09 (s, 1H), 8.47 (s, 1H), 8.39 (s, 1H), 8.33 (s, 1H), 8.00 (d, 1H), 7.81 (brs, 2H), 7.65 (d, 2H), 7.47 (d, 2H), 7.10 (m, 1H), 6.80 (s, 1H), 2.28 (s, 3H).
This example was prepared by substituting 1-isocyanato-2-methylbenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (400 MHz, DMSO-d6) δ 10.65 (s, 1H), 9.03 (s, 1H), 8.39 (s, 1H), 8.34 (s, 1H), 8.11 (brs, 2H), 7.89 (s, 1H), 7.84 (d, 1H), 7.64 (d, 2H), 7.48 (d, 2H), 7.15 (m, 2H), 6.94 (t, 1H), 2.25 (s, 3H).
This example was prepared by substituting 1-isocyanato-4-methoxybenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (400 MHz, DMSO-d6) δ 10.65 (s, 1H), 8.59 (s, 1H), 8.43 (s, 1H), 8.41 (s, 1H), 8.35 (s, 1H), 8.08 (brs, 2H), 7.62 (d, 2H), 7.46 (d, 2H), 7.35 (d, 2H), 6.87 (d, 2H), 3.72 (s, 3H).
This example was prepared by substituting 1-isocyanato-3, 5-dimethylbenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (300 MHz, DMSO-d6) δ 10.64 (s, 1H), 8.64 (s, 1H), 8.47 (s, 1H), 8.37 (s, 1H), 8.32 (s, 1H), 8.02 (brs, 2H), 7.63 (d, 2H), 7.46 (d, 2H), 7.07 (s, 2H), 6.61 (m, 1H), 2.23 (s, 6H).
This example was prepared by substituting 1-fluoro-2-isocyanato-4-trifluoromethylbenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (500 MHz, DMSO-d6) δ 10.69 (s, 1H), 9.21 (s, 1H), 8.88 (d, 1H), 8.64 (dd, 1H), 8.38 (s, 1G), 8.32 (s, 1H), 8.04 (brs, 2H), 7.68 (d, 2H), 7.50 (m, 3H), 7.39 (m, 1H).
This example was prepared by substituting isocyanatobenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (400 MHz, DMSO-d6) δ 10.64 (s, 1H), 8.67 (s, 1H), 8.63 (s, 1H), 8.38 (s, 1H), 8.33 (s, 1H), 8.01 (brs, 2H), 7.63 (d, 2H), 7.46 (m, 4H), 7.28 (m, 2H), 6.97 (m, 1H).
Bromine (0.75 mL) was added dropwise to mixture of 5-amino-4-cyanothiophene-3-carboxylic acid ethyl ester (2.9 g) in dichloromethane (150 mL) at 0° C. The mixture was stirred for 1.5 hours. diluted with dichloromethane, washed with 10% NaHSO3 and brine and dried (MgSO4), filtered and concentrated.
A mixture of EXAMPLE 22A (0.2 g), 1-methyl-4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-1H-pyrazole (0.368 g), Na2CO3 (0.211 g), Pd(PPh3)4 (0.05 g) in DME (4 mL) and water (2 mL) at 120° C. was stirred in a sealed vial for 30 minutes in a Smith Synthesizer microwave oven (at 300 W), cooled to ambient temperature and partitioned between water and ethyl acetate. The extract was washed with brine, dried (MgSO4), filtered and concentrated. The concentrate was flash chromatographed on silica gel with 1% methanot/dichloromethane.
This example was prepared by substituting EXAMPLE 22B for 5-amino-4-cyano-thiophene-3-carboxylic acid ethyl ester in EXAMPLE 1A and EXAMPLE 1B.
This example was prepared by substituting EXAMPLE 22C and 1-chloro-3-isocyanatobenzene for EXAMPLE 1B and 1-isocyanato-3-methylbenzene in EXAMPLES 1C and 1D, respectively. 1H NMR (400 MHz, DMSO-d6) δ 10.63 (s, 1H), 8.85 (s, 1H), 8.76 (s, 1H), 8.32 (s, 1H), 8.09 (s, 1H), 7.71 (m, 1H), 7.61 (s, 1H), 7.55 (d, 2H), 7.45 (d, 2H), 7.28 (m, 2H), 7.01 (m, 3H), 3.85 (s, 3H).
This example was prepared by substituting EXAMPLE 22C for EXAMPLE 1B in EXAMPLE 1D. 1H NMR (400 MHz, DMSO-d6) δ 10.61 (s, 1H), 8.66 (s, 1H), 8.54 (s, 1H), 8.32 (s, 1H), 8.08 (s, 1H), 7.60 (s, 1H), 7.53 (d, 2H), 7.44 (d, 2H), 7.29 (s, 1H), 7.22 (d, 1H), 7.15 (t, 1H), 7.00 (brs, 2H), 6.78 (d, 1H), 3.84 (s, 3H), 2.27 (s, 3H).
This example was prepared by substituting EXAMPLE 22C and 1-fluoro-2-isocyanato-4-methylbenzene for EXAMPLE 1B and 1-isocyanato-3-methylbenzene in EXAMPLES 1C and 1D, respectively. 1H NMR (400 MHz, DMSO-d6) δ 10.63 (s, 1H), 9.08 (s, 1H), 8.44 (d, 1H), 8.33 (s, 1H), 8.08 (s, 1H), 7.99 (dd, 1H), 7.60 (m, 1H), 7.55 (m, 2H), 7.45 (m, 2H), 7.09 (dd, 1H), 7.00 (brs, 2H), 6.80 (m, 1H), 3.85 (s, 3H), 2.27 (s, 3H).
This example was prepared by substituting EXAMPLE 22C and 1-fluoro-4-isocyanato-2-trifluoromethylbenzene for EXAMPLE 1B and 1-isocyanato-3-methylbenzene in EXAMPLES 1C and 1D, respectively. 1H NMR (400 MHz, DMSO-d6) δ 10.64 (s, 1H), 9.01 (s, 1H), 8.82 (s, 1H), 8.32 (s, 1H), 8.09 (s, 1H), 8.00 (dd, 1H), 7.64 (m, 1H), 7.60 (s, 1H), 7.55 (d, 2H), 7.44 (m, 3H), 7.00 (brs, 2H), 3.85 (s, 3H).
This example was prepared by substituting EXAMPLE 22C and 1-fluoro-2-isocyanato-4-trifluoromethylbenzene for EXAMPLE 1B and 1-isocyanato-3-methylbenzene in EXAMPLES 1C and 1D, respectively. 1H NMR (500 MHz, DMSO-d6) δ 10.67 (s, 1H), 9.21 (s, 1H), 8.87 (d, 1H), 8.63 (dd, 1H), 8.33 (s, 1H), 8.10 (s, 1H), 7.59 (m, 3H), 7.48 (m, 3H), 7.39 (m, 1H), 7.02 (brs, 2H), 3.85 (s, 3H).
This example was prepared by substituting EXAMPLE 22C and 1-isocyanato-4-trifluoromethylbenzene for EXAMPLE 1B and 1-isocyanato-3-methylbenzene in EXAMPLES 1C and 1D, respectively. 1H NMR (500 MHz, DMSO-d6) δ 10.67 (s, 1H), 9.08 (s, 1H), 8.84 (s, 1H), 8.33 (s, 1H), 8.10 (s, 1H), 7.65 (m, 4H), 7.60 (s, 1H), 7.56 (d, 2H), 7.47 (d, 2H), 7.02 (brs, 2H), 3.85 (s, 3H).
This example was prepared by substituting EXAMPLE 22C and 4-phenoxyphenylamine for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D. 1H NMR (400 MHz, DMSO-d6) δ 10.73 (s, 1H), 8.33 (s, 1H), 8.10 (s, 1H), 7.63 (t, 4H), 7.39 (t, 2H), 7.13 (t, 1H), 7.01 (m, 5H), 3.85 (s, 3H).
This example was prepared by substituting 4-phenoxyphenylamine for EXAMPLE 1C in EXAMPLE 1D. 1H NMR (300 MHz, DMSO-d6) δ 10.76 (s, 1H), 8.39 (s, 1H), 8.32 (s, 1H), 7.74 (m, 2H), 7.39 (m, 2H), 7.13 (m, 1H), 7.07 (m, 2H), 7.01 (m, 2H).
A mixture of 1-fluoro-4-nitrobenzene (0.5 g), 3-methylphenol (0.383 g), 37% w/w KF—Al2O3 (0.4 g) and 18-crown-6 (0.093 g) in acetonitrile (6 mL) at reflux was stirred for 24 hours, cooled and partitioned between water and ethyl acetate. The extract was washed with water, dried (MgSO4), filtered and concentrated. The concentrate was flash chromatographed on silica gel with 0-10% ethyl acetate/hexanes.
A mixture of EXAMPLE 30A (0.36 g), iron powder (0.45 g) and NH4Cl (0.086 mg) in ethanol (46 mL), THF (17 mL) and water (6 mL) at 85° C. was stirred for 7 hours, cooled to ambient temperature, stirred for 18 hours, heated and filtered through diatomaceous earth (Celite®) while hot. The filtrate was concentrated and partitioned between water and ethyl acetate. The organic layer was washed with brine, dried (MgSO4), filtered and concentrated. The concentrate was flash chromatographed on silica gel with 10% ethyl acetate/hexanes.
This example was prepared by substituting EXAMPLE 22C and 30B for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D. 1H NMR (400 MHz, DMSO-d6) δ 10.73 (s, 1H), 8.33 (s, 1H), 8.10 (s, 1H), 7.63 (m, 3H), 7.26 (t, 1H), 7.03 (m, 2H), 6.99 (brs, 2H), 6.95 (d, 1H), 6.84 (m, 1H), 6.80 (dd, 1H), 3.85 (s, 3H), 2.29 (s, 3H).
This example was prepared by substituting EXAMPLE 22C and 4-(4-chlorophenoxy)-phenylamine (prepared by substituting 4-chlorophenol for 3-methylphenol in EXAMPLE 30B) for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D. 1H NMR (400 MHz, DMSO-d6) δ 10.76 (s, 1H), 8.33 (s, 1H), 8.10 (s, 1H), 7.66 (d, 2H), 7.61 (s, 1H), 7.42 (d, 2H), 7.08 (d, 2H), 7.03 (d, 2H), 6.98 (brs, 2H), 3.85 (s, 3H).
This example was prepared by substituting EXAMPLE 22C and 4-(4-methyl-phenoxy)phenylamine (prepared by substituting 4-methylphenol for 3-methylphenol in EXAMPLE 30B) for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D. 1H NMR (400 MHz, DMSO-d6) δ 10.71 (s, 1H), 8.33 (s, 1H), 8.10 (s, 1H), 7.63 (s, 1H), 7.60 (brs, 2H), 7.19 (d, 2H), 6.96 (m, 6H), 3.85 (s, 3H), 2.29 (s, 3H).
This example was prepared by substituting EXAMPLE 22C and 4-(3-chlorophenoxy)-phenylamine (prepared by substituting 3-chlorophenol for 3-methylphenol in EXAMPLE 30B) for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D. 1H NMR (400 MHz, DMSO-d6) δ 10.78 (s, 1H), 8.33 (s, 1H), 8.10 (s, 1H), 7.68 (d, 2H), 7.62 (s, 1H), 7.40 (t, 1H), 7.19 (m, 1H), 7.11 (d, 2H), 7.06 (t, 1H), 6.97 (m, 3H), 3.85 (s, 3H).
This example was prepared by substituting EXAMPLE 22C and 4-phenylsulfanylphenylamine for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D. 1H NMR (400 MHz, DMSO-d6) δ 10.84 (s, 1H), 8.33 (s, 1H), 8.09 (s, 1H), 7.67 (m, 2H), 7.59 (d, 1H), 7.38 (m, 4H), 7.28 (m, 3H), 6.96 (brs, 2H), 3.84 (s, 3H).
This example was prepared by substituting 4-(4-methylphenoxy)phenylamine (prepared by substituting 4-methylphenol for 3-methylphenol in EXAMPLE 30B) for EXAMPLE 1C in EXAMPLE 1D. 1H NMR (300 MHz, DMSO-d6) δ 10.73 (s, 1H), 8.38 (s, 1H), 8.31 (s, 1H), 7.96 (m, 2H), 7.71 (d, 2H), 7.19 (d, 2H), 7.01 (d, 2H), 6.91 (d, 2H), 2.29 (s, 3H).
This example was prepared as described in EXAMPLES 22B and 22C by substituting 4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-1H-pyrazole for 1-methyl-4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-1H-pyrazole in EXAMPLE 22B and coupling the product therefrom as described in EXAMPLE 1D by substituting 4-phenoxyphenylaamine for EXAMPLE 1C. 1H NMR (400 MHz, DMSO-d6) δ 10.74 (s, 1H), 8.33 (s, 1H), 8.09 (s, 1H), 7.70 (s, 1H), 7.65 (m, 2H), 7.38 (m, 2H), 7.13 (t, 1H), 7.03 (m, 7H).
This example was prepared as described in EXAMPLES 22B and 22C by substituting 4,4,5,5-tetramethyl-2-thiophen-3-yl[1,3,2]dioxaborolane for 1-methyl-4-(4,4,5,5-tetramethyl[1.3.2]dioxaborolan-2-yl)-1H-pyrazole in EXAMPLE 22B and coupling the product therefrom as described in EXAMPLE 1D by substituting 4-phenoxyphenylamine for EXAMPLE 1C. 1H NMR (500 MHz, DMSO-d6) δ 10.71 (s, 1H), 8.37 (s, 1H), 7.85 (m, 1H), 7.68 (m, 1H), 7.58 (d, 2H), 7.39 (t, 2H), 7.28 (d, 1H), 7.13 (t, 2H), 7.01 (t, 5H).
A mixture of EXAMPLE 22A (0.1 g) and 1-methylpiperazine (1 mL) was stirred at 130° C. for 8 hours, cooled and partitioned between water and ethyl acetate. The extract was washed with water and brine and dried (MgSO4), filtered and concentrated.
This example was prepared by substituting EXAMPLE 38A for 5-amino-4-cyano-thiophene-3-carboxylic acid ethyl ester in EXAMPLES 1A-D. 1H NMR (400 MHz, DMSO-d6) δ 10.60 (s, 1H), 8.65 (s, 1H), 8.56 (s, 1H), 8.20 (s, 1H), 7.64 (d, 2H), 7.50 (s, 2H), 7.46 (d, 2H), 7.30 (s, 1H), 7.23 (m, 1H), 7.15 (t, 1H), 6.79 (d, 1H), 3.12 (m, 4H), 2.43 (m, 4H), 2.28 (s, 3H), 2.18 (s, 3H).
1M borane THF in THF (0.28 mL) was added to mixture of N-(4-(formylamino)phenyl)-N′-(3-methylphenyl)urea (0.05 g, prepared by substituting formic acid for EXAMPLE 1B in EXAMPLE 1D) in THF (2 mL) at 0° C. The mixture was stirred for 1.5 hours at ambient temperature, cooled to 0° C., treated with methanolic HCl (2 mL), stirred at reflux for 1 hour, cooled to ambient temperature and concentrated. The concentrate was reconcentrated twice from methanol then flash chromatographed on silica 5% methanol/dichloromethane.
This example was prepared by substituting EXAMPLE 39A for EXAMPLE 1C in EXAMPLE 1D. 1H NMR (500 MHz, DMSO-d6) δ 8.70 (s, 1H), 8.57 (s, 1H), 8.31 (s, 1H), 7.37 (d, 4H), 7.35 (brs, 2H), 7.26 (s, 2H), 7.20 (d, 1H), 7.14 (m, 1H), 7.09 (d, 3H), 6.78 (d, 1H), 3.42 (s, 3H).
A mixture of 3-bromothieno[3,2-c]pyridin-4-ylamine (2 g, prepared as described in WO 05/010009) and PdCl2(dppf)-dichloromethane (0.715 g) in methanol (60 mL) and triethylamine (3.7 mL) in a sealed tube under CO (60 psi) was stirred at 100° C. for 16 hours, cooled to ambient temperature, filtered and concentrated. The concentrate was triturated with water and filtered.
A suspension of EXAMPLE 40A (0.87 g) in 9M HCl (50 mL) was heated to reflux for 18 hours, filtered hot and concentrated.
This example was prepared by substituting EXAMPLE 40B and 4-phenoxyphenylamine for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D. 1H NMR (DMSO-d6, 300 MHz) δ 10.79 (s, 1H), 8.28 (s, 1H), 7.87 (d, 1H), 7.77 (d, 2H), 7.39 (m, 2H), 7.25 (d, 1H), 7.13 (t, 1H), 7.07 (d, 2H), 7.01 (d, 2H), 6.80 (brs, 2H).
This example was prepared by substituting EXAMPLE 40B and 3-phenoxyphenylamine for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D. 1H NMR (DMSO-d6, 300 MHz) δ 10.82 (s, 1H), 8.28 (s, 1H), 7.86 (d, 1H), 7.56 (d, 1H), 7.40 (m, 4H), 7.24 (d, 1H), 7.17 (t, 1H), 7.07 (d, 2H), 6.81 (d, 1H), 6.73 (brs, 2H).
This example was prepared by substituting EXAMPLE 40B and 4-benzylphenylamine for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D. 1H NMR (DMSO-d6, 300 MHz) δ 10.69 (s, 1H), 8.25 (s, 1H), 7.86 (d, 1H), 7.66 (d, 2H), 7.24 (m, 8H), 6.78 (brs, 2H). 3.93 (s, 2H).
This example was prepared by substituting EXAMPLE 40B for EXAMPLE 1B in EXAMPLE 1D. 1H NMR (DMSO-d6, 300 MHz) δ 10.67 (s, 1H), 8.67 (s, 1H), 8.57 (s, 1H), 8.26 (s, 1H), 7.87 (d, 1H), 7.67 (d, 2H), 7.47 (d, 2H), 7.30 (s, 1H), 7.23 (m, 2H), 7.15 (t, 1H), 6.83 (s, 2H), 6.80 (d, 1H), 2.28 (s, 3H).
This example was prepared by substituting EXAMPLE 40B and N-(4-aminophenyl)benzamide for EXAMPLES 1B and 1C, respectively in EXAMPLE 1D. 1H NMR (DMSO-d6, 300 MHz) δ 10.76 (s, 1H), 10.28 (s, 1H), 8.29 (s, 1H), 7.98 (d, 2H), 7.88 (d, 1H), 7.81 (d, 2H), 7.74 (d, 2H), 7.56 (m, 3H), 7.26 (d, 1H), 6.83 (brs, 2H).
A mixture of EXAMPLE 40B (0.73 g) in DMF (30 mL) at ambient temperature was treated with NIS (1.42 g), stirred for 18 hours, diluted with water, treated with 10% aqueous Na2S2O3 and filtered.
This example was prepared by substituting EXAMPLE 45A and (4-aminophenyl)carbamic acid tert-butyl ester for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D. The Boc protecting group was removed by treatment of the product therefrom with TFA as described in EXAMPLE 1C.
A mixture of EXAMPLE 45B (1.93 g), 1-methyl-4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-1H-pyrazole (1.08 g), PdCl2(dppf) (0.19 g) and Na2CO3 (1.3 g) in DME (30 mL) and water (10 mL) at 80° C. was stirred for 18 hours, cooled, treated with water and ethyl acetate and filtered.
A mixture of EXAMPLE 45C (0.03 g) in DMF (0.5 mL) at −20° C. was treated with 1-isocyanato-3-methylbenzene (0.1 mL), the warmed to ambient temperature and stirred for 18 hours and filtered. The filtrant was flash chromatographed on silica gel with 0-8% methanol/dichloromethane. 1H NMR (300 MHz, DMSO-d6) δ 10.70 (s, 1H), 8.67 (s, 1H), 8.57 (s, 1H), 8.33 (s, 1H), 8.14 (d, 1H), 8.06 (s, 1H), 7.86 (d, 1H), 7.67 (d, 2H), 7.47 (d, 2H), 7.30 (s, 1H), 7.23 (d, 1H), 7.15 (t, 1H), 6.82 (s, 2H), 6.79 (d, 1H), 3.93 (s, 3H), 2.28 (s, 3H).
This example was prepared by substituting EXAMPLE 45B and N-(4-aminophenyl)benzamide for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D then by substituting the product thereform for EXAMPLE 45B in EXAMPLE 45C. 1H NMR (DMSO-d6, 300 MHz) δ 10.80 (s, 1H), 10.29 (s, 1H), 8.36 (s, 1H), 8.14 (s, 1H), 8.06 (s, 1H), 7.97 (d, 2H), 7.87 (s, 1H), 7.77 (m, 4H), 7.56 (m, 3H), 6.83 (brs, 2H), 3.93 (s, 3H).
This example was prepared by substituting EXAMPLE 45B and 4-phenoxyphenylamine for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D then by substituting the product thereform for EXAMPLE 45B in EXAMPLE 45C. 1H NMR (DMSO-d6, 300 MHz) δ 10.84 (s, 1H), 8.36 (s, 1H), 8.14 (s, 1H), 8.06 (s, 1H), 7.87 (s, 1H), 7.80 (d, 2H), 7.39 (m, 2H), 7.13 (t, 1H), 7.09 (d, 2H), 7.03 (d, 2H), 6.81 (brs, 2H), 3.93 (s, 3H).
This example was prepared by substituting EXAMPLE 45B and 3-phenoxyphenylamine for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D then by substituting the product therefrom for EXAMPLE 45B in EXAMPLE 45C. 1H NMR (DMSO-d6, 300 MHz) δ 10.85 (s, 1H), 8.35 (s, 1H), 8.13 (s, 1H), 8.05 (s, 1H), 7.85 (s, 1H), 7.58 (d, 1H), 7.46 (m, 2H), 7.42 (d, 2H), 7.17 (t, 1H), 7.08 (d, 2H), 6.81 (m, 1H), 6.73 (brs, 2H), 3.92 (s, 3H).
This example was prepared by substituting EXAMPLE 45B and 4-benzylphenylamine for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D then by substituting the product therefrom for EXAMPLE 45B in EXAMPLE 45C. 1H NMR (DMSO-d6, 300 MHz) δ 10.75 (s, 1H), 8.32 (s, 1H), 8.13 (s, 1H), 8.05 (s, 1H), 7.86 (s, 1H), 7.67 (d, 2H), 7.32-7.18 (m, 7H), 6.79 (brs, 2H), 3.94 (s, 2H), 3.93 (s, 3H).
This example was prepared as described in EXAMPLE 40A and EXAMPLE 40B, except substituting 5-iodo-7-(4-(4-methyl-piperazin-1-yl)cyclohexyl)-7H-pyrrolo[2,3-d]pyrimidin-4-ylamine (WO2005/74603) for 3-bromo-thieno[3,2-c]pyridin-4-ylamine in EXAMPLE 40A.
This example was prepared by substituting EXAMPLE 50A and 4-phenoxyphenylamine for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D. 1HNMR (DMSO-d6, 300 MHz) δ 10.13 (s, 1H), 8.30 (s, 1H), 8.12 (s, 1H), 7.93 (brs, 2H), 7.70-7.74 (m, 1H), 7.66-7.70 (m, 1H), 7.36-7.44 (m, 2H), 7.08-7.17 (m, 1H), 6.98-7.07 (m, 4H), 4.60-4.72 (m, 1H), 3.32 (hidden, 1H), 2.48-2.59 (m, 4H), 2.33-2.48 (m, 4H), 2.15-2.23 (m, 4H), 1.96-2.15 (m, 3H), 1.74-1.85 (m, 2H), 1.53-1.68 (m, 2H).
This example was prepared by substituting EXAMPLE 50A and 3-phenoxyphenylamine for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D. 1HNMR (DMSO-d6, 300 MHz) δ 10.12 (s, 1H), 8.28 (s, 1H), 8.11 (s, 1H), 7.87 (bs, 2H), 7.49-7.56 (m, 1H), 7.33-7.46 (m, 4H), 7.13-7.21 (m, 1H), 7.06-7.10 (m, 1H), 7.03-7.06 (m, 1H), 6.74-6.81 (m, 1H), 4.58-4.71 (m, 1H), 2.32-2.60 (m, 8H), 2.25-2.30 (m, 1H), 1.93-2.24 (m, 7H), 1.73-1.85 (m, 2H), 1.52-1.68 (m, 2H).
This example was prepared by substituting EXAMPLE 50A for EXAMPLE 1B in EXAMPLE 1D. 1H NMR (DMSO-d6, 300 MHz) δ 10.03 (s, 1H), 8.64 (s, 46H), 8.56 (s, 1H), 8.30 (s, 1H), 8.11 (s, 1H), 7.99 (bs, 2H), 7.59-7.63 (m, 1H), 7.56-7.59 (m, 1H), 7.45-7.48 (m, 1H), 7.42-7.45 (m, 1H), 7.31 (s, 1H), 7.20-7.26 (m, 1H), 7.15 (t, 1H), 6.79 (d, 1H), 4.59-4.72 (m, 1H), 2.37-2.51 (m, 9H), 2.28 (s, 3H), 2.20 (s, 3H), 1.96-2.16 (m, 4H), 1.74-1.86 (m, 2H), 1.53-1.68 (m, 2H).
This example was prepared by substituting EXAMPLE 50A and 4-(4-aminophenylsulfanyl)phenylamine for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D. 1HNMR(DMSO-d6, 300 MHz) δ 10.09 (s, 1H), 8.29 (s, 1H), 8.11 (s, 1H), 7.88 (bs, 2H), 7.59-7.63 (m, 1H), 7.56-7.59 (m, 1H), 7.17-7.21 (m, 1H), 7.14-7.17 (m, 1H), 7.08-7.11 (m, 1H), 7.05-7.08 (m, 1H), 6.81-6.83 (m, 1H), 6.79-6.81 (m, 1H), 5.47 (s, 2H), 4.58-4.71 (m, 1H), 2.56-2.70 (m, 9H), 2.20 (s, 3H), 1.94-2.16 (m, 4H), 1.73-1.85 (m, 2H), 1.52-1.67 (m, 2H).
This example was prepared by substituting EXAMPLE 50A and 4-benzylphenylamine for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D. 1HNMR (DMSO-d6, 300 MHz) δ 10.04 (s, 1H), 8.29 (s, 1H), 8.11 (s, 1H), 7.92 (bs, 2H), 7.60-7.63 (m, 1H), 7.57-7.60 (m, 1H), 7.15-7.34 (m, 7H), 4.59-4.72 (m, 1H), 3.93 (s, 2H), 2.37-2.59 (m, 8H), 2.25-2.29 (m, 1H), 2.22 (s, 3H), 1.94-2.15 (m, 4H), 1.74-1.85 (m, 2H), 1.53-1.68 (m, 2H).
This example was prepared by substituting EXAMPLE 50A and 4-benzenesulfonylphenylamine for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D. 1HNMR(DMSO-d6, 300 MHz) δ 10.41 (s, 1H), 8.34 (s, 1H), 8.13 (s, 1H), 7.96 (s, 5H), 7.92-7.94 (m, 1H), 7.87 (bs, 2H), 7.59-7.73 (m, 3H), 4.59-4.72 (m, 1H), 2.36-2.48 (m, 8H), 2.16-2.22 (m, 4H), 1.94-2.16 (m, 4H), 1.75-1.85 (m, 2H), 1.53-1.69 (m, 2H).
This example was prepared as described in EXAMPLES 40A and 40B by substituting 3-iodo-1-(4-morpholin-4-ylcyclohexyl)-1 H-pyrazolo[3,4-d]pyrimidin-4-ylamine (prepared as described in WO 05/74603) for 3-bromothieno[3,2-c]pyridin-4-ylamine in EXAMPLE 40A.
This example was prepared by substituting EXAMPLE 56A and 4-phenoxyphenylamine for EXAMPLES 1B and 1C, respectively, in EXAMPLE 1D. 1H NMR (DMSO-d6, 300 MHz) δ 10.41 (s, 1H), 8.53 (s, 1H), 8.25 (s, 1H), 8.06 (bs, 1H), 7.83-7.87 (m, 1H), 7.79-7.83 (m, 1H), 7.36-7.45 (m, 2H), 7.10-7.17 (m, 1H), 6.99-7.09 (m, 4H), 4.83-4.96 (m, 1H), 3.55-3.63 (m, 4H), 2.47-2.57 (m, 4H), 2.29-2.42 (m, 1H), 2.09-2.29 (m, 2H), 1.96-2.09 (m, 4H), 1.40-1.57 (m, 2H).
This example was prepared by substituting 3-bromo-7-iodo-thieno[3,2-c]pyridin-4-ylamine (prepared as described in WO 05/10009) for EXAMPLE 45B in EXAMPLE 45C.
A mixture of 4-ethynylphenylamine (0.3 g), 4,4,5,5-tetramethyl[1,3,2]-dioxaborolane (0.56 mL) and ZrCp2ClH (0.083 g) in THF (6 mL) was stirred at 50° C. for 1.5 hours and concentrated. The concentrate was flash chromatographed on silica gel with 30% ethyl acetate/hexanes.
This example was prepared by substituting EXAMPLES 57A and 57B for EXAMPLE 45B and 1-methyl-4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-1H-pyrazole, respectively, in EXAMPLE 45C. 1H NMR (300 MHz, DMSO-d6) δ 3.92 (s, 3H) 5.32 (s, 2H) 6.01 (s, 2H) 6.57 (d, 2H) 6.86 (d, 1H) 7.27-7.42 (m, 3H) 7.60 (s, 1H) 7.85 (s, 1H) 8.11 (s, 1H).
This example was prepared by substituting EXAMPLE 57B for EXAMPLE 45C in EXAMPLE45D.
This example was prepared by substituting EXAMPLES 57A and 58A for EXAMPLE 45B and 1-methyl-4-(4,4,5 5-tetramethyl[1,3,2]dioxaborolan-2-yl)-1H-pyrazole, respectively, in EXAMPLE 45C. 1H NMR (300 MHz, DMSO-d6) δ 2.28 (s, 3H) 3.93 (s, 3H) 6.08 (s, 2H) 6.80 (d, 1H) 7.00 (d, 1H) 7.16 (t, 1H) 7.20-7.27 (m, 1H) 7.31 (s, 1H) 7.44-7.54 (m, 2H) 7.54-7.68 (m, 3H) 7.73 (s, 1H) 7.86 (s, 1H) 8.01 (s, 1H) 8.12 (s, 1H) 8.62 (s, 1H) 8.79 (s, 1H).
This example was prepared by substituting 1-ethynyl-4-phenoxybenzene for 4-ethynylphenylamine in EXAMPLE 57B then substituting the product therefrom and EXAMPLE 57A for 1-methyl-4-(4,4,5,5-tetramethyl [1,3,2]dioxaborolan-2-yl)-1H-pyrazole and EXAMPLE 45B, respectively, in EXAMPLE 45C. 1H NMR (300 MHz, DMSO-d6) δ 3.93 (s, 3H) 6.10 (s, 2H) 6.99-7.11 (m, 5H) 7.16 (t, 1H) 7.36-7.47 (m, 2H) 7.61-7.78 (m, 4H) 7.86 (s, 1H) 8.02 (s, 1H) 8.12 (s, 1H).
This example was prepared by substituting EXAMPLE 57A and 2-(2-biphenyl-4-yl-vinyl)-4,4,5,5-tetramethyl[1,3,2]dioxaborolane for EXAMPLE 45B and 1-methyl-4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-1H-pyrazole, respectively, in EXAMPLE 45C. 1H NMR (300 MHz, DMSO-d6) δ 3.93 (s, 3 H) 6.11 (s, 2 H) 7.13 (d, 1H) 7.33-7.42 (m, 1H) 7.48 (t, 2H) 7.68-7.85 (m, 8H) 7.87 (s, 1H) 8.03 (s, 1H) 8.13 (s, 1H).
EXAMPLES 61-65 were prepared following the procedures of EXAMPLE 45D and substituting the appropriate isocyanate (X) for 1-isocyanato-3-methylbenzene.
X=1-isocyanatobenzene. 1H NMR (300 MHz, DMSO-d6) δ 10.72 (s, 1H), 8.70 (s, 1H), 8.66 (s, 1H), 8.33 (s, 1H), 8.14 (s, 1H), 8.06 (s, 1H), 7.87 (s, 1H), 7.67 (d, J=8.8 Hz, 2H), 7.43-7.50 (m, 4H), 7.25-7.31 (m, 2H), 6.97 (t, J=7.3Hz, 1H), 6.83 (s, 2H), 3.93 (s, 3H).
X=1-fluoro-3-isocyanatobenzene. 1H NMR (300 MHz, DMSO-d6) δ 10.73 (s, 1H), 8.88 (s, 1H), 8.75 (s, 1H), 8.34 (s, 1H), 8.14 (s, 1H), 8.06 (s, 1H), 7.87 (s, 1H), 7.68 (d, J=8.8 Hz, 2H), 7.44-7.53 (m, 3H), 7.31 (td, J=8.1, 6.8 Hz, 1H), 7.12 (ddd, J=8.1, 2.0, 0.7 Hz, 1H), 6.83 (s, 2H), 6.74-6.82 (m, 1H), 3.93 (s, 3H).
X=isocyanatocyclohexane. 1H NMR (300 MHz, DMSO-d6) δ 10.65 (s, 1H), 8.35 (s, 1H), 8.31 (s, 1H), 8.13 (s, 1H), 8.05 (s, 1H), 7.86 (s, 1H), 7.59 (d, J=9.2Hz, 2H), 7.38 (d, J=9.2 Hz, 2H), 6.82 (s, 2H), 6.08 (d, J=8.1 Hz, 1H), 3.93 (s, 3H), 1.75-1.85 (m, 2H), 1.60-1.72 (m, 2H), 1.47-1.59 (m, 1H), 1.08-1.40 (m, 5H).
X=1-isocyanato-4-methylbenzene. 1H NMR (300 MHz, DMSO-d6) δ 10.71 (s, 1H), 8.67 (s, 1H), 8.57 (s, 1H), 8.33 (s, 1H), 8.14 (d, J=0.7Hz, 1H), 8.06 (s, 1H), 7.87 (d, J=1.0 Hz, 1H), 7.66 (d, J=9.2 Hz, 2H), 7.46 (d, J=9.2 Hz, 2H), 7.34 (d, J=8.5 Hz, 2H), 7.08 (d, J=8.5 Hz, 2H), 6.83 (s, 2H), 3.93 (s, 3H), 2.24 (s, 3H).
X=1-isocyanato-2-methylbenzene. 1H NMR (300 MHz, DMSO-d6) δ 10.72 (s, 1H), 9.05 (s, 1H), 8.33 (s, 1H), 8.14 (s, 1H), 8.06 (s, 1H), 7.91 (s, 1H), 7.83-7.87 (m, 2H), 7.68 (d, J=8.8 Hz, 2H), 7.48 (d, J=8.8 Hz, 2H), 7.11-7.20 (m, 2H), 6.94 (td, J=7.4, 1.2 Hz, 1H), 6.83 (s, 2H), 3.93 (s, 3H), 2.25 (s, 3H).
This example was prepared by substituting (3-aminophenyl)carbamic acid tert-butyl ester for (4-aminophenyl)carbamic acid tert-butyl ester in EXAMPLE 45B.
This example was prepared by substituting EXAMPLE 66A and isocyanatobenzene for EXAMPLE 45C and 1-isocyanato-3-methylbenzene, respectively, in EXAMPLE 45D. 1H NMR (300 MHz, DMSO-d6) δ 10.79 (s, 1H), 8.77 (s, 1H), 8.60 (s, 1H), 8.36 (s, 1H), 8.14 (s, 1H), 8.07 (s, 1H), 7.99 (s, 1H), 7.87 (s, 1H), 7.43-7.49 (m, 2H), 7.24-7.38 (m, 5H), 6.97 (t, J=7.3 Hz, 1H), 6.80 (s, 2H), 3.93 (s, 3H).
This example was prepared by substituting EXAMPLE 66A and 1-isocyanato-2-methylbenzene for EXAMPLE 45C and 1-isocyanato-3-methylbenzene, respectively, in EXAMPLE 45D. 1H NMR (300 MHz, DMSO-d6) δ 10.81 (s, 1H), 9.15 (s, 1H), 8.37 (s, 1H), 8.14 (s, 1H), 8.07 (s, 1H), 8.00-8.03 (m, 1H), 7.86-7.90 (m, 3H), 7.31-7.38 (m, 1H), 7.25-7.31 (m, 2H), 7.11-7.20 (m, 2H), 6.94 (td, J=7.4, 1.2Hz, 1H), 6.80 (s, 2H), 3.93 (s, 3H), 2.26 (s, 3H).
This example was prepared by substituting EXAMPLE 66A and I -isocyanato-4-methylbenzene for EXAMPLE 45C and 1-isocyanato-3-methylbenzene, respectively, in EXAMPLE 45D. 1H NMR (300 MHz, DMSO-d6) δ 10.78 (s, 1H), 8.73 (s, 1H), 8.49 (s, 1H), 8.36 (s, 1H), 8.14 (s, 1H), 8.06 (s, 1H), 7.96-7.98 (m, 1H), 7.87 (d, J=0.7 Hz, 1H), 7.26-7.37 (m, 5H), 7.09 (d, J=8.5 Hz, 2H), 6.80 (s, 2H), 3.93 (s, 3H), 2.24 (s, 3H).
This example was prepared by substituting EXAMPLE 66A for EXAMPLE 45C in EXAMPLE 45D. 1H NMR (300 MHz, DMSO-d6) δ 10.79 (s, 1H), 8.80 (s, 1H), 8.55 (s, 1H), 8.36 (s, 1H), 8.14 (s, 1H), 8.06 (s, 1H), 7.99 (s, 1H), 7.87 (s, 1H), 7.26-7.38 (m, 4H), 7.20-7.26 (m, 1H), 7.15 (t, J=7.6 Hz, 1H), 6.76-6.82 (m, 3H), 3.93 (s, 3H), 2.28 (s, 3H).
This example was prepared by substituting EXAMPLE 45A and N-(3-aminophenyl)benzamide for EXAMPLE 1B and EXAMPLE 1C, respectively, in EXAMPLE 1D and substituting the product therefrom for EXAMPLE 45B in EXAMPLE 45C. 1H NMR (300 MHz, DMSO-d6) δ 10.86 (s, 1H), 10.35 (s, 1H), 8.36-8.39 (m, 2H), 8.14 (s, 1H), 8.07 (s, 1H), 7.98 (dd, J=8.3, 1.5 Hz, 2H), 7.87 (d, J=1.0 Hz, 1H), 7.50-7.63 (m, 4H), 7.44-7.48 (m, 1H), 7.35 (t, J=8.0 Hz, 1H), 6.82 (s, 2H), 3.93 (s, 3H).
This example was prepared as described in EXAMPLE 1D by substituting EXAMPLE 45A and tert-butyl 4-aminopiperidine-1-carboxylate for EXAMPLE 1B and EXAMPLE 1C, respectively, and substituting the product therefrom for EXAMPLE 45B in EXAMPLE 45C. The Boc group was removed with TFA as described in EXAMPLE 1C.
This example was prepared by substituting EXAMPLE 71A and isocyanatobenzene for 45C and 1-isocyanato-3-methylbenzene, respectively, in EXAMPLE 45D. 1H NMR (300 MHz, DMSO-d6) δ 8.84 (d, J=7.5 Hz, 1H), 8.54 (s, 1H), 8.12 (s, 1H), 8.11 (s, 1H), 8.02 (s, 1H), 7.84 (d, J=1.0 Hz, 1H), 7.46 (d, J=7.8 Hz, 2H), 7.23 (t, J=8.0 Hz, 2H), 6.97 (s, 2H), 6.93 (t, J=7.3 Hz, 1H), 3.98-4.17 (m, 3H), 3.92 (s, 3H), 2.97 (t, J=11.5 Hz, 2H), 1.89 (dd, J=12.7, 3.2 Hz, 2H), 1.44-1.59 (m, 2H).
A mixture of EXAMPLE 71A (75 mg), benzoic acid (26 mg), HoBT (57 mg) and NMM (0.23 mL) in DMF (2 mL) at 0° C. was treated with EDCI (80 mg), allowed to warm to a room temperature, stirred for 5 hours, diluted with water and extracted with ethyl acetate. The extract was dried (Na2SO4), filtered and concentrated. The concantrate was triturated with dichloromethane, filtered and air dried. 1H NMR (300 MHz, DMSO-d6) δ 8.86 (d, J=7.5 Hz, 1H), 8.12 (s, 1H), 8.11 (d, J=0.7 Hz, 1H), 8.02 (s, 1H), 7.84 (d, J=1.0 Hz, 1H), 7.44-7.49 (m, 3H), 7.36-7.41 (m, 2H), 6.95 (s, 2H), 4.33-4.52 (brm, 1H), 4.04-4.17 (brm, 1H), 3.92 (s, 3H), 3.52-3.71 (brm, 1H), 2.94-3.27 (brm, 2H), 1.77-2.03 (brm, 2H), 1.39-1.64 (brm, 2H).
This example was prepared by substituting tert-butyl trans-4-aminocyclohexylcarbamate for EXAMPLE 71A in EXAMPLE 72 and removing the Boc with TFA as described in EXAMPLE 1C.
This example was prepared by coupling EXAMPLES 45A and 73A as described in EXAMPLE 72 and substituting the product therefrom for EXAMPLE 45B in EXAMPLE 45C. 1H NMR (300 MHz, DMSO-d6) δ 8.80 (d, J=7.8 Hz, 1H), 8.27 (d, J=8.1 Hz, 1H), 8.11 (s, 1H), 8.09 (s, 1H), 8.02 (s, 1H), 7.82-7.88 (m, 3H), 7.42-7.55 (m, 3H), 6.97 (s, 2H), 3.92 (s, 3H), 3.73-3.85 (brm, 2H), 1.89-2.01 (brm, 4H), 1.39-1.57 (m, 4H).
An ice cold solution of tert-butyl trans-4-aminocyclohexylcarbamate (250 mg) and isocyanatobenzene (0.11 mL) in DMF (5 mL) was treated with NMM (0.22 mL), stirred at ambient temperature for 5 hours, diluted with water and filtered. The filtrate was dissolved in dichloromethane (10 mL) and treated with TFA (1 mL). The mixture was stirred at ambient temperature for 3 hours and concentrated.
This example was prepared by coupling EXAMPLES 45A and 74A as described in EXAMPLE 72 and substituting the product therefrom for EXAMPLE 45B in EXAMPLE 45C. 1H NMR (300 MHz, DMSO-d6) δ 8.77 (d, J=7.8 Hz, 1H), 8.32 (s, 1H), 8.11 (s, 1H), 8.08 (s, 1H), 8.02 (s, 1H), 7.83 (s, 1H), 7.37 (d, J=7.5 Hz, 2H), 7.17-7.25 (m, 2H), 6.96 (s, 2H), 6.88 (t, J=7.3 Hz, 1H), 6.10 (d, J=7.5 Hz, 1H), 3.92 (s, 3H), 3.74-3.87 (brm, 1H), 3.38-3.49 (brm, 1H), 1.89-1.99 (brm, 4H), 1.21-1.54 (m, 4H).
This example was prepared by substituting 1-fluoro-2-isocyanatobenzene for isocyanatobenzene in EXAMPLE 74A then EXAMPLE 74B. 1H NMR (300 MHz, DMSO-d6) δ 8.77 (d, J=7.8 Hz, 1H), 8.09-8.17 (m, 3H), 8.08 (s, 1H), 8.02 (s, 1H), 7.83 (s, 1H), 7.16 (ddd, J=11.8, 8.1, 1.5 Hz, 1H), 7.07 (t, J=7.1 Hz, 1H), 6.96 (s, 2H), 6.87-6.95 (m, 1H), 6.62 (d, J=7.5 Hz, 1H), 3.92 (s, 3H), 3.75-3.88 (m, 1H), 3.39-3.51 (m, 1H), 1.88-2.02 (m, 4H), 1.37-1.56 (m, 2H), 1.20-1.36 (m, 2H).
This example was prepared by substituting tert-butyl 4-aminobenzylcarbamate for tert-butyl trans-4-aminocyclohexylcarbamate in EXAMPLES 74A and 74B. 1H NMR (300 MHz, DMSO-d6) δ 9.42 (t, J=5.8 Hz, 1H), 8.71 (s, 1H), 8.70 (s, 1H), 8.16 (s, 1H), 8.11 (d, J=0.7 Hz, 1H), 8.02 (s, 1H), 7.84 (d, J=0.7 Hz, 1H), 7.41-7.47 (m, 4H), 7.24-7.31 (m, 4H), 7.02 (s, 2H), 6.92-6.99 (m, 1H), 4.45 (d, J=5.8Hz, 2H), 3.92 (s, 3H).
This example was prepared by substituting tert-butyl 3-aminobenzylcarbamate for tert-butyl trans-4-aminocyclohexylcarbamate in EXAMPLES 74A and 74B. 1H NMR (300 MHz, DMSO-d6) δ 9.48 (t, J=5.9 Hz, 1H), 8.68 (s, 1H), 8.62 (s, 1H), 8.19 (s, 1H), 8.11 (s, 1H), 8.02 (s, 1H), 7.84 (s, 1H), 7.36-7.47 (m, 4H), 7.23-7.30 (m, 3H), 7.03 (s, 2H), 6.93-7.01 (m, 2H), 4.49 (d, J=5.8 Hz, 2H), 3.92 (s, 3H).
This example was prepared by substituting 3-bromo-7-iodothieno[3,2-c]pyridin-4-amine for EXAMPLE 45B in EXAMPLE 45C and substituting the product therefrom for 3-bromo-thieno[3,2-c]pyridn-4-ylamine in EXAMPLES 40A and 40B.
This example was prepared by coupling EXAMPLE 78A and 4-(aminomethyl)-N-phenylpiperidine-1-carboxamide (prepared by substituting tert-butyl piperidin-4-ylmethylcarbamate for tert-butyl trans-4-aminocyclohexylcarbamate in EXAMPLE 74A) as described in EXAMPLE 72. 1H NMR (300 MHz, DMSO-d6) δ 8.97 (t, J=5.6Hz, 1H), 8.45 (s, 1H), 8.12 (s, 1H), 8.11 (s, 1H), 8.02 (s, 1H), 7.84 (s, 1H), 7.45 (d, J=7.8 Hz, 2H), 7.18-7.25 (m, 2H), 6.99 (s, 2H), 6.91 (t, J=7.3 Hz, 1H), 4.14 (d, J=12.9 Hz, 2H), 3.92 (s, 3H), 3.23 (t, J=5.9 Hz, 2H), 2.79 (t, J=11.9 Hz, 2H), 1.72-1.86 (m, 3H), 1.08-1.24 (m, 2H).
This example was prepared by substituting 78A and tert-butyl 4-aminobenzylcarbamate for benzoic acid and 71A, respectively, in EXAMPLE 72, removing the Boc group with TFA as described in EXAMPLE 1C and substituting the product therefrom for tert-butyl trans-4-aminocyclohexylcarbamate in EXAMPLE 74A. 1H NMR (300 MHz, DMSO-d6) δ 10.78 (s, 1H), 8.53 (s, 1H), 8.35 (s, 1H), 8.14 (s, 1H), 8.06 (s, 1H), 7.86 (s, 1H), 7.71 (d, J=7.8 Hz, 2H), 7.39-7.43 (m, 2H), 7.32 (d, J=8.1 Hz, 2H), 7.19-7.25 (m, 2H), 6.87-6.93 (m, 1H), 6.80 (s, 2H), 6.59 (t, J=6.4 Hz, 1H), 4.29 (d, J=5.8 Hz, 2H), 3.93 (s, 3H).
This example was prepared by substituting EXAMPLE 78A and tert-butyl 3-aminobenzylcarbamate for benzoic acid and EXAMPLE 71A, respectively, in EXAMPLE 72, removing the Boc group with TFA as described in EXAMPLE 1C and substituting the product therefrom for tert-butyl trans-4-aminocyclohexylcarbamate in EXAMPLE 74A. 1H NMR (300 MHz, DMSO-d6) δ 10.81 (s, 1H), 8.56 (s, 1H), 8.34 (s, 1H), 8.13 (d, J=0.7 Hz, 1H), 8.06 (s, 1H), 7.86 (d, J=0.7 Hz, 1H), 7.72-7.74 (m, 1H), 7.62-7.66 (m, 1H), 7.39-7.43 (m, 2H), 7.35 (t, J=8.0 Hz, 1H), 7.18-7.25 (m, 2H), 7.10 (d, J=7.8 Hz, 1H), 6.89 (t, J=7.3 Hz, 1H), 6.78 (s, 2H), 6.64 (t, J=5.9 Hz, 1H), 4.32 (d, J=6.4Hz, 2H), 3.93 (s, 3H).
A mixture of (1S,4S)-4-(tert-butoxycarbonylamino)cyclohexanecarboxylic acid (245 mg) in toluene (10 mL) was treated with triethylamine (0.14 nmL) and DPPA (0.22 mL), heated at 70° C. for 45 minutes, cooled to ambient temperature and treated with aniline (0.188 mL). The mixture was stirred overnight at ambient temperature, diluted with ether and washed with 0.5 N HCl, saturated NaHCO3, water and brine and dried (Na2SO4), filtered and concentrated. The concentrate was purified by silica gel chromatography to provide tert-butyl (1S,4S)-4-(3-phenylureido)cyclohexylcarbamate which was dissolved in dichloromethane (2 mL) and TFA (2 mL), stirred at ambient temperature for 12 hours and concentrated.
This example was prepared by substituting EXAMPLE 78A and EXAMPLE 81A for benzoic acid and EXAMPLE 71A respectively, in EXAMPLE 72. 1H NMR (300 MHz, DMSO-d6) δ 8.78 (d, J=6.8 Hz, 1H), 8.41 (s, 1H), 8.11 (s, 1H), 8.07 (s, 1H), 8.02 (s, 1H), 7.84 (s, 1H), 7.37 (d, J=7.5 Hz, 2H), 7.21 (t, J=7.8 Hz, 2H), 6.85-6.93 (m, 3H), 6.17 (d, J=6.8 Hz, 1H), 3.92 (s, 3H), 3.83-3.90 (m, 1H), 3.66-3.73 (m, 1H), 1.62-1.79 (m, 8H).
This example was prepared by substituting racemic cis-3-(tert-butoxycarbonylamino)cyclohexanecarboxylic acid for cis-4-(tert-butoxycarbonylamino)cyclohexanecarboxylic acid in EXAMPLES 81A and 81B. 1H NMR (300 MHz, DMSO-d6) δ 8.81 (d, J=7.8 Hz, 1H), 8.30 (s, 1H), 8.11 (s, 1H), 8.07 (s, 1H), 8.02 (s, 1H), 7.83 (s, 1H), 7.37 (d, J=7.8 Hz, 2H), 7.21 (t, J=7.8 Hz, 2H), 6.93 (s, 2H), 6.88 (t, J=7.1 Hz, 1H), 6.16 (d, J=7.8 Hz, 1H), 3.91 (s, 3H), 3.78-3.94 (m, 1H), 3.47-3.62 (m, 1H), 2.11-2.20 (m, 1H), 1.73-1.92 (m, 3H), 1.00-1.48 (m, 4H).
This example was prepared by substituting (±)-(1R,3S)-3-(tert-butoxycarbonylamino)cyclohexanecarboxylic acid and aniline for benzoic acid and EXAMPLE 71A respectively, in EXAMPLE 72 and removing the Boc with TFA as described in EXAMPLE 1C.
This example was prepared by substituting EXAMPLE 78A and EXAMPLE 83A for benzoic acid and EXAMPLE 71A respectively, in EXAMPLE 72. 1H NMR (300 MHz, DMSO-d6) δ 9.91 (s, 1H), 8.85 (d, J=7.8 Hz, 1H), 8.11 (s, 1H), 8.09 (s, 1H), 8.01 (s, 1H), 7.83 (s, 1H), 7.60 (d, J=7.8 Hz, 2H), 7.28 (t, J=8.0 Hz, 2H), 7.02 (t, J=7.3 Hz, 1H), 6.95 (s, 2H), 3.91 (s, 3H), 3.83-3.97 (m, 1H), 2.00-2.09 (m, 1H), 1.77-1.96 (m, 3H), 1.13-1.61 (m, 4H).
4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (2 g) was added portionwise to an ice cold suspension of NaH (280 mg) in DMF (25 mL). The mixture was stirred at 0° C. for 30 minutes, treated with (2-bromoethoxy)(tert-butyl)diphenylsilane (4.16 g), warmed to 50° C. for 2 hours, quenched with water and extracted with ethyl acetate. The extract was dried (Na2SO4), filtered and concentrated, and the concentrate was purified by silica gel chromatography.
This example was prepared by substituting EXAMPLE 78A and tert-butyl 3-aminobenzylcarbamate for benzoic acid and EXAMPLE 71A respectively, in EXAMPLE 72.
This example was prepared by substituting EXAMPLE 84B and EXAMPLE 84A for EXAMPLE 45B and 1-methyl-4-(4,4,5,5-tetramethyl-[ 1,3,2]dioxaborolan-2-yl)-1H-pyrazole in EXAMPLE 45C, removing the Boc with TFA as described in EXAMPLE 1C and substituting the product therefrom for tert-butyl (1R,4R)-4-aminocyclohexylcarbamate in EXAMPLE 74A.
EXAMPLE 84C (0.71 g) and 1M TBAF in THF (1.8 mL) in THF (10 mL) was stirred at ambient temperature for 4 hours, diluted with water and extracted with dichloromethane and methanol. The extract, with the solid at the layer interface, was combined, concentrated and chromatographed on silica gel. The product was further purified by triturating with DMF/water/methanol. 1H NMR (300 MHz, DMSO-d6) δ 10.85 (s, 1H), 8.57 (s, 1H), 8.39 (s, 1H), 8.16 (d, J=0.7 Hz, 1H), 8.08 (s, 1H), 7.90 (d, J=0.7 Hz, 1H), 7.71-7.74 (m, 1H), 7.64 (d, J=7.5 Hz, 1H), 7.41 (dd, J=8.6, 1.2 Hz, 2H), 7.35 (t, J=8.0 Hz, 1H), 7.18-7.25 (m, 2H), 7.11 (d, J=7.8 Hz, 1H), 6.94 (s, 2H), 6.89 (t, J=7.3 Hz, 1H), 6.64 (t, J=6.1 Hz, 1H), 4.95 (t, J=5.3 Hz, 1H), 4.32 (d, J=6.1 Hz, 2H), 4.23 (t, J=5.6 Hz, 2H), 3.80 (q, J=5.1 Hz, 2H).
A mixture of EXAMPLE 84D (164 mg) in dimethylacetamide (2.5 mL) was treated with (tBuO)2PNEt2 (0.31 mL) and tetrazole (132 mg), stirred at ambient temperature for 2 hours, cooled to −10° C. and treated with 30% H2O2 (0.1 mL). The mixture was stirred at ambient temperature for 2.5 hours, treated with of 30% H2O2 (0.3 mL), stirred for 3 hours and partitioned between 10% Na2S2O3 and ethyl acetate. The extract was dried (Na2SO4), filtered and concentrated, and the concentrate was purified by silica gel chromatography.
A mixture of EXAMPLE 85A (90 mg) in methanol (5 mL) was treated with 4M HCl in dioxane (0.2 mL), stirred for 1 hour, diluted with diethylether and filtered. 1H NMR (300 MHz, DMSO-d6) δ 11.09 (s, 1H), 8.90 (s, 1H), 8.90 (s, 2H), 8.76 (s, 1H), 8.33 (d, J=0.7 Hz, 1H), 8.07 (s, 1H), 8.01 (d, J=1.0 Hz, 1H), 7.63-7.68 (m, 2H), 7.35-7.47 (m, 3H), 7.13-7.28 (m, 3H), 6.89 (t, J=7.3 Hz, 1H), 6.74-6.81 (m, 1H), 4.46 (t, J=5.1 Hz, 2H), 4.33 (d, J=4.1 Hz, 2H), 4.20-4.27 (m, 2H).
This example was prepared by substituting EXAMPLE 22C and 2-fluoro-1-isocyanato-3-(trifluoromethyl)benzene for EXAMPLE 1B and 1-isocyanato-3-methylbenzene, respectively, in EXAMPLES 1C and 1D, respectively. 1H NMR (400 MHz, DMSO-d6) δ 10.65 (s, 1H,) 9.18 (s, 1H), 8.82 (d, J=2.46 Hz, 1H), 8.45 (m, 1H), 8.33 (s, 1H), 8.09 (s, 1H), 7.60 (m, 1H), 7.57 (d, J=8.90 Hz, 2H), 7.47 (d, J=9.21 Hz, 2H), 7.35 (m, 2H), 7.00 (brs, 2H) 3.85 (s, 3H).
This example was prepared by substituting EXAMPLE 22C and isocyanatobenzene for EXAMPLE 1B and 1-isocyanato-3-methylbenzene, respectively, in EXAMPLES 1C and 1D, respectively. 1H NMR (500 MHz, DMSO-d6) δ 10.64 (s, 1H), 8.69 (s, 1H), 8.64 (s, 1H), 8.33 (s, 1H), 8.09 (s, 1H), 7.60 (s, 1H), 7.54 (d, J=9.15 Hz, 2H), 7.45 (m, 4H), 7.28 (m, 2H), 7.02 (brs, 2H), 6.96 (t, J=7.32 Hz, 1H), 3.85 (s, 3H).
This example was prepared as described in EXAMPLES 22B-C by substituting 4,4,5,5-tetramethyl-2-thiophen-3-yl-[1,3,2]dioxaborolane for 1-methyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-pyrazole in EXAMPLE 22B and coupling as described in EXAMPLE 1D but substituting 1-(4-aminophenyl)-3-phenylurea for EXAMPLE 1C. 1H NMR (400 MHz, DMSO-d6) δ 10.58 (s, 1H), 8.66 (s, 1H), 8.61 (s, 1H), 8.36 (s, 1H), 7.83 (m, 1H), 7.67 (m, 2H), 7.45 (m, 5H), 7.27 (m, 3H), 7.07 (brs, 2H), 6.96 (t, J=7.36 Hz, 1H).
This example was prepared by substituting morpholine for 1-methylpiperazine in EXAMPLE 38A and following the procedures of EXAMPLE 1, but substituting the product therefrom for 5-amino-4-cyano-thiophene-3-carboxylic acid ethyl ester in EXAMPLE 1A and isocyanatobenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (500 MHz, DMSO-d6) δ 10.64 (s, 1H), 8.68 (s, 1H), 8.64 (s, 1H), 8.22 (s, 1H), 7.67 (d, J=8.85 Hz, 2H), 7.50 (brs, 2H), 7.46 (t, J=9.15 Hz, 4H), 7.28 (m, 2H), 6.97 (t, J=7.32 Hz, 1H), 3.70 (m, 4H), 3.10 (m, 4H).
This example was prepared as described in EXAMPLE 1 by substituting 3-isocyanatothiophene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (400 MHz, DMSO-d6) δ 10.63 (s, 1H), 8.89 (s, 1H), 8.63 (s, 1H), 8.37 (s, 1H), 8.32 (s, 1H), 7.98 (brs, 2H), 7.63 (d, J=8.90 Hz, 2H), 7.47 (d, J=8.90 Hz, 2H), 7.43 (m, 1H), 7.28 (dd, J=3.07, 1.23 Hz, 1H), 7.05 (dd, J=4.91, 1.23 Hz, 1H).
This example was prepared as described in EXAMPLE 1 by substituting isocyanatocyclopentane for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (400 MHz, DMSO-d6) δ 10.57 (s, 1H), 8.35 (s, 1H), 8.31 (s, 1H), 8.25 (s, 1H), 7.92 (brs, 2H), 7.56 (d, J=8.90 Hz, 2H), 7.38 (d, J=9.21 Hz, 2H), 6.11 (d, J=7.06 Hz, 1H), 3.94 (m, 1H), 1.84 (m, 2H), 1.63 (m, 2H), 1.53 (m, 2H), 1.36 (m, 2H).
This example was prepared as described in EXAMPLE 1 by substituting 3-isocyanatopyridine for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (400 MHz, DMSO-d6) δ 10.65 (s, 1H), 8.83 (s, 2H), 8.62 (s, 1H), 8.37 (s, 1H), 8.32 (s, 1H), 8.19 (d, J=3.38 Hz, 1H), 7.95 (m, 1H), 7.96 (brs, 2H), 7.65 (d, J=8.90 Hz, 2H), 7.48 (d, J=8.90 Hz, 2H), 7.32 (m, 1H).
This example was prepared as described in EXAMPLE 1C by substituting 1-isocyanato-4-nitrobenzene and 5-methylisoxazol-3-amine for 1-isocyanato-3-methylbenzene and (4-aminophenyl)carbamic acid tert-butyl ester, respectively, in EXAMPLE 1C.
A mixture of EXAMPLE 93A (700 mg), iron powder (830 mg), NH4Cl (155 mg) in ethanol (25 mL), THF (28 mL) and water (11 mL) at 85° C. was stirred for 9 hours, cooled to ambient temperature and filtered through diatomaceous earth (CELITE®) with ethanol. The filtrate was concentrated and the concentrate was purified by silica gel chromatography.
This example was prepared by substituting EXAMPLE 93B for EXAMPLE 1C in EXAMPLE 1D. 1H NMR (400 MHz, DMSO-d6) δ 10.71 (s, 1H), 9.44 (s, 1H), 8.87 (s, 1H), 8.46 (s, 1H), 8.39 (s, 1H), 8.28 (brs, 2H), 7.65 (d, J=8.90 Hz, 2H), 7.47 (d, J=9.21 Hz, 2H), 6.53 (s, 1H), 2.37 (s, 3H).
This example was prepared as described in EXAMPLE 1 by substituting isocyanatocyclopropane for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (300 MHz, DMSO-d6) δ 10.62 (s, 1H), 8.39 (s, 1H), 8.34 (s, 1H), 8.31 (s, 1H), 7.92 (brs, 2H), 7.56 (d, J=9.16 Hz, 2H), 7.41 (d, J=9.16 Hz, 2H), 6.37 (s, 1H), 2.54 (m, 1H), 0.63 (m, 2H), 0.40 (m, 2H).
This example was prepared as described in EXAMPLE 1 by substituting 2,4-difluoro-1-isocyanatobenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (500 MHz, DMSO-d6) δ 10.67 (s, 1H), 9.05 (s, 1H), 8.49 (s, 1H), 8.37 (s, 1H), 8.32 (s, 1H), 8.10 (m, 1H), 7.65 (d, J=8.54 Hz, 4H), 7.47 (d, J=8.54 Hz, 2H), 7.31 (t, J=8.85 Hz, 1H), 7.05 (t, J=7.93 Hz, 1H).
This example was prepared as described in EXAMPLE 1 by substituting 1,2-difluoro-4-isocyanatobenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (500 MHz, DMSO-d6) δ 10.67 (s, 1H), 8.87 (s, 1H), 8.77 (s, 1H), 8.37 (s, 1H), 8.32 (s, 1H), 7.95 (brs, 2H), 7.68 (m, 1H), 7.64 (d, J=8.85 Hz, 2H), 7.47 (d, J=8.85 Hz, 2H), 7.34 (m, 1H), 7.12 (d, J=9.15 Hz, 1H).
A mixture of 3-(morpholinomethyl)aniline (0.46 g), triethylamine (0.37 mL) and 4-nitrophenylcarbonochloridate (0.53 g) at ambient temperature was stirred for 2 hours, treated with triethylamine (0.37 mL) and tert-butyl 4-aminophenylcarbamate (0.5 g), stirred for 18 hours and partitioned between water and ethyl acetate. The extract was washed with water and brine and dried (Na2SO4), filtered and concentrated. The concentrate was purified by silica gel chromatography to provide tert-butyl 4-(3-(3-(morpholinomethyl)phenyl)ureido)phenylcarbamate, which was dissolved in dichloromethane (30 mL), cooled in an ice bath, treated with TFA (1.8 mL), stirred for 30 minutes, warmed at ambient temperature, stirred for 18 hours and concentrated with a toluene/methanol azeotrope.
This example was prepared by substituting EXAMPLE 97A for EXAMPLE 1C in EXAMPLE 1D. 1H NMR (400 MHz, DMSO-d6) δ 10.63 (s, 1H), 8.65 (s, 1H), 8.63 (s, 1H), 8.37 (s, 1H), 8.32 (s, 1H), 7.96 (brs, 2H), 7.63 (d, J=8.90 Hz, 2H), 7.47 (d, J=8.90 Hz, 3H), 7.34 (d, J=8.90 Hz, 1H), 7.23 (t, J=7.67 Hz, 1H), 6.92 (d, J=7.36Hz, 1H), 3.59 (m, 4H), 3.47 (s, 2H), 2.40 (s, 4H).
This example was prepared by substituting EXAMPLE 74A for EXAMPLE 1C in EXAMPLE 1D. 1H NMR (400 MHz, DMSO-d6) δ 9.34 (brs, 1H), 8.83 (d, J=7.67 Hz, 1H), 8.37 (s, 1H), 8.30 (s, 1H), 8.28 (s, 1H), 8.04 (brs, 2H), 7.37 (m, 2H), 7.21 (m, 2H), 6.88 (m, 1H), 6.08 (d, J=6.44 Hz, 1H), 3.44 (brs, 1H), 1.94 (m, 4H), 1.47 (m, 2H), 1.28 (m, 2H).
This example was prepared as described in EXAMPLE 93 by substituting 3,5-dimethylisoxazol-4-amine for 5-methylisoxazol-3-amine. 1H NMR (300 MHz, DMSO-d6) δ 10.66 (s, 1H), 8.84 (s, 1H), 8.40 (s, 1H), 8.34 (s, 1H), 8.01 (brs, 2H), 7.70 (s, 1H), 7.61 (d, J=9.16 Hz, 2H), 7.46 (d, J=8.82 Hz, 2H), 2.29 (s, 3H), 2.13 (s, 3H).
This example was prepared as described in EXAMPLE 93 by substituting thiazol-2-amine for 5-methylisoxazol-3-amine. 1H NMR (400 MHz, DMSO-d6) δ 10.67 (s, 1H) 10.46 (s, 1H), 8.98 (s, 1H), 8.38 (s, 1H), 8.32 (s, 1H), 7.98 (brs, 2H), 7.67 (d, J=8.9 Hz, 2H), 7.50 (d, J=8.90 Hz, 2H), 7.37 (d, J=3.68 Hz, 1H), 7.11 (d, J=3.07 Hz, 1H).
This example was prepared as described in EXAMPLE 93 by substituting isoxazol-3-amine for 5-methylisoxazol-3-amine. 1H NMR (500 MHz, DMSO-d6) δ 10.69 (s, 1H), 9.58 (s, 1H), 8.86 (s, 1H), 8.74 (s, 1H), 8.38 (s, 1H), 8.32 (s, 1H), 7.83 (brs, 2H), 7.67 (d, J=8.24 Hz, 2H), 7.48 (d, J=8.54 Hz, 2H), 6.85 (s, 1H).
This example was prepared as described in EXAMPLE 1 by substituting tert-butyl piperidin-4-ylcarbamate and isocyanatobenzene for (4-aminophenyl)carbamic acid tert-butyl ester and 1-isocyanato-3-methylbenzene, respectively, in EXAMPLE 1C. 1H NMR (400 MHz, DMSO-d6) δ 9.10 (brs, 1H), 8.85 (d, J=7.67 Hz, 1H), 8.53 (s, 1H), 8.34 (s, 1H), 8.26 (s, 1H), 7.94 (brs, 1H), 7.46 (d, J=7.67 Hz, 2H), 7.22 (m, 2H), 6.93 (t, J=7.36 Hz, 1H), 4.14 (d, J=13.50 Hz, 2H), 4.06 (m, 1H), 2.95 (t, J=11.66 Hz, 2H), 1.88 (d, J=12.27 Hz, 2H), 1.53 (m, 2H).
This example was prepared as described in EXAMPLE 1 by substituting (3-aminophenyl)carbamic acid tert-butyl ester and isocyanatobenzene for (4-aminophenyl)carbamic acid tert-butyl ester and 1-isocyanato-3-methylbenzene, respectively, in EXAMPLE 1B. 1H NMR (500 MHz, DMSO-d6) δ 10.74 (s, 1H), 8.78 (s, 1H), 8.61 (s, 1H), 8.41 (s, 1H), 8.32 (s, 1H), 8.12 (brs, 1H), 7.97 (m, 1H), 7.46 (d, J=7.63 Hz, 2H), 7.34 (m, 1H), 7.29 (t, J=8.24 Hz, 5H), 6.98 (t, J=7.32 Hz, 1H).
A solution of EXAMPLE 1A (750 mg) in THF (34 mL) at −78° C. was treated with 2M LDA in THF (5.1 mL), stirred for 2 hours, treated with iodine (855 mg) in THF (6 mL), stirred for 1 hour, warmed to and at 0° C., stirred for for 2 hours, quenched with saturated NH4Cl and extracted with ethyl acetate. The extract was washed with 10% Na2SO3 and brine and dried (MgSO4), filtered and concentrated. The concentrate was purified by silica gel chromatography.
EXAMPLE 104A (50 mg), 3-methoxyprop-1-yne (0.015 ml), Cl2Pd(PPh3)2 (5 mg), CuI (0.8 mg), triethylamine (0.36 mL) and DMF (0.18 mL) was degassed with nitrogen, heated in a sealed tube at 60° C. for 40 minutes with stirring in a Smith Synthesizer microwave oven (at 200 W). The mixture was partitioned between water and dichloromethane and the extract was washed with brine and dried (MgSO4), filtered and concentrated. The concentrate and was purified by silica gel chromatography.
This example was prepared as described in EXAMPLE 1 by substituting EXAMPLE 104B for EXAMPLE 1A in EXAMPLE 1B and isocyanatobenzene for 1-isocyanato-3-methylbenzene in EXAMPLE 1C. 1H NMR (500 MHz, DMSO-d6) δ 10.87 (s, 1H), 8.70 (s, 1H), 8.64 (s, 1H), 8.39 (s, 1H), 7.47 (m, 10H), 6.97 (s, 1H), 4.38 (s, 2H), 3.22 (s, 3H).
This example was prepared as described in EXAMPLE 104 by substituting ethynyltrimethylsilane for 3-methoxyprop-1-yne. 1H NMR (400 MHz, DMSO-d6) δ 10.84 (s, 1H), 8.71 (s, 1H), 8.64 (s, 1H), 8.40 (s, 1H), 7.65 (d, J=8.90 Hz, 2H), 7.47 (t, J=8.90 Hz, 6H), 7.28 (t, J=8.59,Hz, 2H), 6.97 (t, J=7.36 Hz, 1H), 5.08 (s, 1H).
This example was prepared as described in EXAMPLE 104 by substituting 3-ethynylthiophene for 3-methoxyprop-1-yne. 1H NMR (500 MHz, DMSO-d6) δ 10.94 (s, 1H), 8.71 (s, 1H), 8.65 (s, 1H), 8.40 (s, 1H), 7.89 (m, 1H), 7.70 (d, J=8.85 Hz, 2H), 7.66 (m, 1H), 7.47 (m, 6H), 7.28 (t, J=7.63 Hz, 2H), 7.10 (d, J=5.19 Hz, 1H), 6.97 (t, J=7.32 Hz, 1H).
This example was prepared as described in EXAMPLE 104 by substituting N,N-dimethylprop-2-yn-1-amine for 3-methoxyprop-1-yne. 1H NMR (400 MHz, DMSO-d6) δ 10.84 (s, 1H), 8.69 (s, 1H), 8.64 (s, 1H), 8.38 (s, 1H), 7.65 (d, J=9.21 Hz, 2H), 7.46 (m, 6H), 7.27 (t, J=8.59 Hz, 2H), 6.97 (t, J=7.36 Hz, 1H), 3.54 (s, 2H), 2.12 (s, 6H).
This example was prepared as described in EXAMPLE 1D by substituting N-(4-aminophenyl)-2-fluorobenzamide for EXAMPLE 1C. 1H NMR (500 MHz, DMSO-d6) δ 10.74 (s, 1H), 10.45 (s, 1H), 8.40 (s, 1H), 8.34 (s, 1H), 8.02 (brs, 2H), 7.71 (m, 5H), 7.58 (m, 1H), 7.35 (m, 2H).
This example was prepared as described in EXAMPLE 1D by substituting N-(4-aminophenyl)-3-fluorobenzamide for EXAMPLE 1C. 1H NMR (500 MHz, DMSO-d6) δ 10.75 (s, 1H), 10.36 (s, 1H), 8.40 (s, 1H), 8.33 (s, 1H), 7.78 (m, 8H), 7.60 (s, 1H), 7.46 (s, 1H).
This example was prepared as described in EXAMPLE 1D by substituting N-(4-aminophenyl)-4-fluorobenzamide for EXAMPLE 1C. 1H NMR (500 MHz, DMSO-d6) δ 10.74 (s, 1H), 10.30 (s, 1H), 8.41 (s, 1H), 8.34 (s, 1H), 8.05 (m, 2H), 7.90 (brs, 2H), 7.78 (d, J=8.24 Hz, 2H), 7.71 (d, J=8.24 Hz, 2H), 7.37 (t, J=8.85, 8.24 Hz, 1H).
This example was prepared as described in EXAMPLE 1D by substituting N-(4-aminophenyl)-2-methylbenzamide for EXAMPLE 1C. 1H NMR (400 MHz, DMSO-d6) δ 10.70 (s, 1H), 10.30 (s, 1H), 8.40 (s, 1H), 8.32 (s, 1H), 8.01 (brs, 2H), 7.76 (d, J=8.90 Hz, 2H), 7.68 (d, J=8.90 Hz, 2H), 7.46 (d, J=7.67 Hz, 1H), 7.39 (m, 1H), 7.30 (m, 2H), 2.40 (s, 3H).
This example was prepared as described in EXAMPLE 1D by substituting N-(4-aminophenyl)-3-methylbenzamide for EXAMPLE 1C. 1H NMR (400 MHz, DMSO-d6) δ 10.71 (s, 1H), 10.22 (s, 1H), 8.40 (s, 1H), 8.33 (s, 1H), 8.03 (brs, 2H), 7.77 (m, 4H), 7.70 (d, J=9.21 Hz, 2H), 7.40 (m, 2H), 2.41 (s, 3H).
A solution of CaCl2 (104 mg) in ethanol (2.3 mL) was treated with methyl 3-(3-(4-aminophenyl)ureido)benzoate (50 mg) in THF (2.3 mL) and NaBH4 (71 mg), and the mixture was stirred at reflux for 18 hours, treated with NaBH4 (280 mg) in 4 portions over 8 hours, cooled to ambient temperature and concentrated. The concentrate was treated with water and washed with dichloromethane. The heterogeneous water layer was filtered, and the solid was collected, washed with water and air dried.
This example was prepared as described in EXAMPLE 1D by substituting EXAMPLE 113A for EXAMPLE 1C. 1H NMR (500 MHz, DMSO-d6) δ 10.69 (s, 1H), 8.69 (s, 1H), 8.66 (s, 1H), 8.43 (s, 1H), 8.36 (s, 1H), 7.96 (brs, 2H), 7.63 (d, J=8.85 Hz, 2H), 7.48 (d, J=8.85 Hz, 2H), 7.43 (s, 1H), 7.32 (d, J=8.24 Hz, 1H), 7.22 (t, J=7.93 Hz, 1H), 6.92 (d, J=7.63 Hz, 1H), 4.47 (s, 2H), 3.70 (brs, 1H).
This example was prepared by substituting tert-butyl 3-aminobenzylcarbamate for EXAMPLE 1C in EXAMPLE 1D, removing the Boc with TFA as described in EXAMPLE 1C and substituting the product therefrom and isocyanatobenzene for EXAMPLE 45C and 1-isocyanato-3-methylbenzene, respectively, in EXAMPLE 45D. 1H NMR (500 MHz, DMSO-d6) δ 10.75 (s, 1H), 8.57 (s, 1H), 8.39 (s, 1H), 8.32 (s, 1H), 7.97 (br s, 2H), 7.69 (s, 1H), 7.62 (d, J=7.32 Hz, 1H), 7.41 (d, J=7.63 Hz, 2H), 7.35 (t, J=7.63 Hz, 1H), 7.22 (t, J=7.32 Hz, 2H), 7.11 (d, J=7.32 Hz, 1H), 6.89 (t, J=6.71 Hz, 1H), 6.64 (s, 1H), 4.32 (d, J=5.19 Hz, 2H).
This example was prepared as described in EXAMPLE 1 by substituting (3-aminophenyl)carbamic acid tert-butyl ester and 1-isocyanato-2-methylbenzene for (4-aminophenyl)carbamic acid tert-butyl ester and 1-isocyanato-3-methylbenzene, respectively, in EXAMPLE 1B. 1H NMR (500 MHz, DMSO-d6) δ 10.74 (s, 1H), 9.15 (s, 1H), 8.41 (s, 1H), 8.33 (s, 1H), 8.00 (s, 1H), 7.88 (m, 4H), 7.30 (m, 3H), 7.16 (m, 2H), 6.95 (t, J=7.32 Hz, 1H), 2.26 (s, 3H).
This example was prepared by substituting tert-butyl 3-aminobenzylcarbamate for EXAMPLE 1C in EXAMPLE 1D, removing the Boc with TFA as described in EXAMPLE 1C and substituting the product therefrom for EXAMPLE 45C in EXAMPLE 45D. 1H NMR (500 MHz, DMSO-d6) δ 10.75 (s, 1H), 8.48 (s, 1H), 8.39 (s, 1H), 8.33 (s, 1H), 7.90 (br s, 2H), 7.68 (s, 1H), 7.62 (d, J=7.93 Hz, 1H), 7.35 (t, J=7.93 Hz, 1H), 7.25 (s, 1H), 7.18 (d, J=7.93 Hz, 1H), 7.10 (m, 2H), 6.71 (d, J=7.32 Hz, 1H), 6.62 (t, J=5.80 Hz, 1H), 4.32 (d, J=5.80 Hz, 2H), 2.24 (s, 3H).
This example was prepared by substituting tert-butyl 3-aminobenzylcarbamate for EXAMPLE 1C in EXAMPLE 1D, removing the Boc with TFA as described in EXAMPLE 1C and substituting the product therefrom and 1-fluoro-3-isocyanatobenzene for EXAMPLE 45C and 1-isocyanato-3-methylbenzene, respectively, in EXAMPLE 45D. 1H NMR (500 MHz, DMSO-d6) δ 10.75 (m, 1H), 8.84 (m, 1H), 8.39 (m, 1H), 8.32 (m, 1H), 7.98 (m, 2H), 7.68 (m, 1H), 7.62 (d, J=8.24 Hz, 1H), 7.47 (d, J=12.21 Hz, 1H), 7.35 (t, =7.93 Hz, 1H), 7.24 (m, 1H), 7.11 (d, J=7.63 Hz, 1H), 7.05 (d, J=9.15 Hz, 1H), 6.72 (m, 2H), 4.32 (d, J=6.10 Hz, 2H).
This example was prepared as described in EXAMPLE 1 by substituting (3-aminophenyl)carbamic acid tert-butyl ester for (4-aminophenyl)carbamic acid tert-butyl ester in EXAMPLE 1B. 1H NMR (500 MHz, DMSO-d6) δ 10.74 (m, 1H), 8.77 (m, 1H), 8.55 (m, 1H), 8.41 (m, 1H), 8.33 (m, 1H), 7.97 (m, 1H), 7.75 (m, 2H), 7.29 (m, 5H), 7.16 (t, J=7.63 Hz, 1H), 6.80 (d, J=7.32 Hz, 1H), 2.28 (s, 3H).
This example was prepared as described in EXAMPLE 1 by substituting (3-aminophenyl)carbamic acid tert-butyl ester and 1-isocyanato-4-methylbenzene for (4-aminophenyl)carbamic acid tert-butyl ester and 1-isocyanato-3-methylbenzene, respectively, in EXAMPLE 1B. 1H NMR (500 MHz, DMSO-d6) δ 10.73 (s, 1H), 8.74 (s, 1H), 8.51 (s, 1H), 8.41 (s, 1H), 8.33 (s, 1H), 7.96 (s, 1H), 7.77 (br s, 2H), 7.30 (m, 5H), 7.09 (m, 2H), 2.24 (s, 3H).
This example was prepared as described in EXAMPLE 1 by substituting (3-aminophenyl)carbamic acid tert-butyl ester and 1-fluoro-2-isocyanatobenzene for (4-aminophenyl)carbamic acid tert-butyl ester and 1-isocyanato-3-methylbenzene, respectively, in EXAMPLE 1B. 1H NMR (500 MHz, DMSO-d6) δ 10.75 (s, 1H), 9.21 (s, 1H), 8.54 (d, J=2.14 Hz, 1H), 8.41 (s, 1H) 8.33 (s, 1H), 8.17 (t, J=8.24 Hz, 1H), 7.98 (s, 1H), 7.73 (br s, 2H), 7.35 (m, 1H), 7.30 (m, 2H), 7.24 (m, 1H), 7.15 (t, J=7.32 Hz, 1H), 7.01 (m, 1H).
This example was prepared as described in EXAMPLE 1 by substituting (3-aminophenyl)carbamic acid tert-butyl ester and 1-fluoro-3-isocyanatobenzene for (4-aminophenyl)carbamic acid tert-butyl ester and 1-isocyanato-3-methylbenzene, respectively, in EXAMPLE 1B. 1H NMR (500 MHz, DMSO-d6) δ 10.75 (s, 1H), 8.85 (s, 2H), 8.41 (s, 1H), 8.32 (s, 1H), 7.97 (s, 1H), 7.96 (br s, 2H), 7.50 (d, J=11.90 Hz, 1H), 7.36 (m, 1H), 7.29 (m, 3H), 7.12 (d, J=7.93 Hz, 1H), 6.79 (t, J=6.10 Hz, 1H).
This example was prepared as described in EXAMPLE 1 by substituting (3-aminophenyl)carbamic acid tert-butyl ester and 1-fluoro-4-isocyanatobenzene for (4-aminophenyl)carbamic acid tert-butyl ester and 1-isocyanato-3-methylbenzene, respectively, in EXAMPLE 1B. 1H NMR (500 MHz, DMSO-d6) δ 10.73 (m, 1H), 8.78 (m, 1H), 8.65 (m, 1H), 8.40 (m, 1H), 8.33 (m, 1H), 7.97 (m, 1H), 7.78 (m, 2H), 7.47 (m, 2H), 7.33 (m, 1H), 7.28 (m, 2H), 7.13 (t, J=8.85 Hz, 2H).
This example was prepared by substituting tert-butyl 3-aminobenzylcarbamate for EXAMPLE 1C in EXAMPLE 1D, removing the Boc with TFA as described in EXAMPLE 1C and substituting the product therefrom and 1-isocyanato-3-(trifluoromethyl)benzene for EXAMPLE 45C and 1-isocyanato-3-methylbenzene, respectively, in EXAMPLE 45D. 1H NMR (500 MHz, DMSO-d6) δ 10.75 (s, 1H), 9.04 (s, 1H), 8.39 (s, 1H), 8.32 (s, 1H), 7.97 (br s, 2H), 7.63 (m, 6H), 7.35 (s, 1H), 7.11 (s, 1H), 6.82 (s, 1H), 4.34 (s, 2H).
This example was prepared by substituting 2-(2-aminothiazol-5-yl)-N-(3-fluorophenyl)acetamide for EXAMPLE 1C in EXAMPLE 1D. 1H NMR (500 MHz, DMSO-d6) δ 12.95 (br s, 1H), 10.47 (s, 1H), 8.61 (s, 1H), 8.32 (s, 1H), 7.97 (br s, 2H), 7.61 (d, J=11.90 Hz, I1H), 7.44 (s, 1H), 7.34 (m, 2H), 6.90 (t, J=6.41 Hz, 1H), 3.91 (s, 2H).
A solution of 4-amino-N-methoxythieno[2,3-d]pyrimidine-5-carboxamide (3 mmol) (prepared by substituting O-methylhydroxylamine for EXAMPLE 1C in EXAMPLE 1D) in THF (12 mL) was added to a suspension of LAH (235 mg) in THF (12 mL) at −78° C. The mixture was stirred for 30 minutes, treated sequentially with water (0.24 mL), 1M NaOH (0.24 mL) and water, (0.72 mL), filtered through diatomaceous earth (CELITE®) and concentrated.
A solution of (4-nitrobenzyl)triphenylphosphonium bromide (1.66 g) in THF (20 mL) at 0° C. was treated with 1.6M n-butyllithium in hexanes (2.2 mL), stirred for 40 minutes, treated with EXAMPLE 125A in THF (20 mL), stirred at 0° C. for 3 hours and at ambient temperature for 18 hours, treated with 5% methanol in dichloromethane, washed with water and dried (Na2SO4), filtered and concentrated. The concentrate was triturated with methanol and air dried.
This example was prepared as described for EXAMPLE 93B and substituting EXAMPLE 125B for EXAMPLE 93A.
A mixture of EXAMPLE 125C (110 mg) and 5% Pd on carbon (50 mg) in methanol (10 mL) was shaken under hydrogen (60 psi) at 50° C. for 40 hours, filtered and concentrated.
This example was prepared as described for EXAMPLE 45D and substituting EXAMPLE 125D and isocyanatobenzene for EXAMPLE 45C and 1-isocyanato-3-methylbenzene, respectively. 1H NMR (400 MHz, DMSO-d6) δ 8.65 (s, 1H), 8.61 (s, 1H), 8.25 (s, 1H), 7.44 (d, J=7.98 Hz, 2H), 7.35 (d, J=8.59 Hz, 2H), 7.27 (t, J=7.98 Hz, 2H), 7.15 (d, J=8.29 Hz, 2H), 7.10 (s, 1H), 6.99 (s, 2H), 6.95 (m, 1H), 3.22 (t, J=8.29 Hz, 2H), 2.90 (t, J=8.29 Hz, 2H).
This example was prepared by substituting 1-(4-aminophenyl)-3-(3-(3-hydroxypropoxy)phenyl)urea for EXAMPLE 1C in EXAMPLE 1D. 1H NMR (500 MHz, DMSO-d6) δ 10.68 (s, 1H), 8.70 (s, 1H), 8.66 (s, 1H), 8.48 (br s, 1H), 8.41 (s, 1H), 8.36 (s, 1H), 7.95 (br s, 1H), 7.63 (d, J=8.85 Hz, 2H), 7.47 (d, J=8.85 Hz, 2H), 7.22 (m, 1H), 7.16 (t, J=8.24 Hz, 1H), 6.89 (d, J=7.93 Hz, 1H), 6.54 (m, 1H), 4.00 (t, J=6.41 Hz, 2H), 3.56 (t, J=6.41 Hz, 2H), 1.86 (m, 2H).
Example 127 This example was prepared by substituting tert-butyl 4-(aminomethyl)phenylcarbamate for EXAMPLE 1C in EXAMPLE 1D, removing the Boc with TFA as described in EXAMPLE 1C and substituting the product therefrom and isocyanatobenzene for EXAMPLE 45C and 1-isocyanato-3-methylbenzene, respectively, in EXAMPLE 45D. 1H NMR (400 MHz, DMSO-d6) δ 9.50 (t, J=6.14Hz, 1H), 9.06 (s, 1H), 8.68 (s, 1H), 8.66 (s, 1H), 8.31 (s, 1H), 8.27 (s, 1H), 7.81 (br s, 1H), 7.43 (m, 4H), 7.27 (m, 4H), 6.96 (t, J=7.36 Hz, 1H), 4.44 (d, J=5.83 Hz, 2H).
This example was prepared by substituting tert-butyl 4-(aminomethyl)phenylcarbamate for EXAMPLE 1C in EXAMPLE 1D, removing the Boc with TFA as described in EXAMPLE 1C and substituting the product therefrom for EXAMPLE 45C in EXAMPLE 45D. 1H NMR (400 MHz, DMSO-d6) δ 9.52 (t, J=5.83 Hz, 1H), 9.21 (br s, 1H), 8.67 (s, 1H) 8.59 (s, 1H), 8.34 (s, 1H), 8.30 (s, 1H), 7.92 )br s, 1H), 7.43 (d, J=8.59 Hz, 2H), 7.29 (d, J=5.83 Hz, 2H), 7.25 (s, 1H), 7.21 (d, J=8.59 Hz, 1H), 7.14 (m, 1H), 6.78 (d, J=7.98 Hz, 1H), 4.44 (d, J=5.83 Hz, 2H), 2.27 (s, 3H).
This example was prepared by substituting tert-butyl 4-(aminomethyl)phenylcarbamate for EXAMPLE 1C in EXAMPLE 1D, removing the Boc with TFA as described in EXAMPLE 1C and substituting the product therefrom and 1-fluoro-3-isocyanatobenzene for EXAMPLE 45C and 1-isocyanato-3-methylbenzene, respectively, in EXAMPLE 45D. 1H NMR (400 MHz, DMSO-d6) δ 9.52 (t, J=5.83 Hz, 1H), 9.18 (brs, 1H), 8.95 (s, 1H), 8.80 (s, 1H), 8.34 (s, 1H), 8.30 (s, 1H), 7.91 (br s, 1H), 7.49 (m, 1H), 7.43 (d, J=8.59 Hz, 2H), 7.29 (m, 3H), 7.11 (m, 1H), 6.77 (s, 1H), 4.45 (d, J=5.83 Hz, 2H).
The foregoing is meant to illustrate the invention but not to limit it. Variations and changes obvious to one skilled in the art are intended to be within the scope of the invention as defined in the claims.
This application claims priority to U.S. Provisional Parent Application Ser. No. 60/749,074, filed Dec. 8, 2005.
| Number | Date | Country | |
|---|---|---|---|
| 60749074 | Dec 2005 | US |
