IP Library Granted Patent US 7,868,177
Granted Patent B2
US 7,868,177 · App. 11/709,994 · Granted Jan 11, 2011

Multi-cyclic compounds and method of use

Assignee: Amgen Inc.
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Quick Facts
Patent No.
US 7,868,177
App. No.
11/709,994
Granted
Jan 11, 2011
Kind
B2
Abstract

The present invention relates to chemical compounds having a general formula I wherein A, B, C 1 , C 2 , D, L 1 , L 2 and R 3-4 are defined herein, and synthetic intermediates, which are capable of modulating various protein kinase receptor enzymes and, thereby, influencing various disease states and conditions related to the activities of such kinases. For example, the compounds are capable of modulating Tie-2 and Aurora kinase enzymes thereby influencing angiogenesis and the process of cell cycle and cell proliferation, respectively, to treat cancer and cancer-related diseases. The invention also includes pharmaceutical compositions, including the compounds, and methods of treating disease states related to the activity of various protein kinases.

Claims (241)

1. A compound of Formula I:

or a stereoisomer or pharmaceutically acceptable salt thereof, wherein

A is a ring selected from

wherein each of A 1 and A 3 independently, is N or CR 8 and A 2 is NR 9 , O or S;

B is a fully unsaturated 5-6 membered first monocyclic ring, said first ring (1) formed of carbon atoms optionally including 1-3 heteroatoms selected from O, N, or S, (2) optionally fused to a partially or fully saturated or fully unsaturated 5-6 membered second monocyclic ring formed of carbon atoms optionally including 1-3 heteroatoms selected from O, N, or S, and (3) wherein 0, 1, 2 or 3 atoms of each of said first and second ring is optionally substituted independently with 1-4 substituents of R 5 ;

C 1 is N or CR 10 ;

C 2 is N or CH, provided that (1) when C 1 is N then C 2 is CH or (2) when C 1 is CR 10 then C 2 is N;

D is

wherein D 1 is N or CR 11 ;

D 2 is N or CR 12 ;

R 1 is H, OR 14 , SR 14 , OR 15 , SR 15 , NR 14 R 15 , NR 15 R 15 , (CHR 15 ) n R 14 , (CHR 15 ) n R 15 or R 15 ,

wherein n is 0, 1, 2, 3 or 4;

R 1a is H, CN or C 1-10 alkyl;

alternatively R 1 taken together with either of R 11 and R 1a and the carbon or nitrogen atoms to which they are attached form a partially or fully unsaturated 5- or 6-membered ring of carbon atoms optionally including 1-3 heteroatoms selected from O, N and S, and the ring optionally substituted independently with 1-3 substituents of R 15 , SR 14 , OR 14 , SR 15 , OR 15 , OC(O)R 15 , COOR 15 , C(O)R 15 , C(O)NR 15 R 15 , NR 14 R 15 or NR 15 R 15 ; and

R 2 is SR 14 , OR 14 , SR 15 , OR 15 , NR 14 R 15 , NR 15 R 15 , C(O)R 14 , C(O)R 15 , COOR 15 , OC(O)R 15 , C(O)C(O)R 15 , C(O)NR 14 R 15 , C(O)NR 15 R 15 , NR 15 C(O)R 14 , NR 15 C(O)R 15 , NR 15 C(O)NR 14 R 15 , NR 15 C(O)NR 15 R 15 , NR 15 C(O)C(O)R 15 , NR 15 (COOR 15 ), OC(O)NR 15 R 15 , S(O) 2 R 14 , S(O) 2 R 15 , S(O) 2 NR 14 R 15 , S(O) 2 NR 15 R 15 , NR 15 S(O) 2 NR 14 R 15 , NR 15 S(O) 2 NR 15 R 15 , NR 15 S(O) 2 R 14 , NR 15 S(O) 2 R 15 or R 15 ;

L 1 is NR 3 , O, S, C(O), S(O), SO 2 or CR 3 R 3 ;

L 2 is NR 3 , O, S, C(O), S(O), SO 2 or CR 3 R 3 ;

each of R 3 and R 4 , independently, is SR 14 , OR 14 , SR 15 , OR 15 , NR 14 R 15 , NR 15 R 15 , C(O)R 14 , C(O)R 15 , COOR 15 , OC(O)R 15 , C(O)C(O)R 15 , C(O)NR 14 R 15 , C(O)NR 15 R 15 , NR 15 C(O)R 14 , NR 15 C(O)R 15 , NR 15 C(O)NR 14 R 15 , NR 15 C(O)NR 15 R 15 , NR 15 C(O)C(O)R 15 , NR 15 (COOR 15 ), OC(O)NR 15 R 15 , S(O) 2 R 14 , S(O) 2 R 15 , S(O) 2 NR 14 R 15 , S(O) 2 NR 15 R 15 , NR 15 S(O) 2 NR 15 R 15 , NR 15 S(O) 2 R 14 , NR 15 S(O) 2 R 15 , NR 15 S(O) 2 NR 14 R 15 , NR 15 C(O)C(O)NR 14 R 15 , NR 15 C(O)C(O)NR 15 R 15 or R 15 ;

alternatively, either of R 3 or R 4 , independently, taken together with R 10 and the carbon atoms to which they are attached form a partially or fully unsaturated 5- or 6-membered ring of carbon atoms optionally including 1-3 heteroatoms selected from O, N, or S, and the ring optionally substituted independently with 1-3 substituents of R 13 , R 14 or R 15 ;

each R 5 , independently, is SR 14 , OR 14 , SR 15 , OR 15 , NR 14 R 15 , NR 15 R 15 , C(O)R 14 , C(O)R 15 , COOR 15 , OC(O)R 15 , C(O)C(O)R 15 , C(O)NR 14 R 15 , C(O)NR 15 R 15 , NR 15 C(O)R 14 , NR 15 C(O)R 15 , NR 15 C(O)NR 14 R 15 , NR 15 C(O)NR 15 R 15 , NR 15 C(O)C(O)R 15 , NR 15 (COOR 15 ), OC(O)NR 15 R 15 , S(O) 2 R 14 , S(O) 2 R 15 , S(O) 2 NR 14 R 15 , S(O) 2 NR 15 R 15 , NR 15 S(O) 2 NR 15 R 15 , NR 15 S(O) 2 R 14 , NR 15 S(O) 2 R 15 , NR 15 S(O) 2 NR 14 R 15 , NR 15 C(O)C(O)NR 14 R 15 , NR 15 C(O)C(O)NR 15 R 15 or R 15 ;

each of R 6 , R 7 and R 8 , independently, is R 13 , R 14 or R 15 ;

alternatively, R 6 and R 7 taken together with the carbon atoms to which they are attached form a partially or fully unsaturated 5- or 6-membered ring of carbon atoms optionally including 1-3 heteroatoms selected from O, N, or S, and the ring optionally substituted independently with 1-4 substituents of R 13 , R 14 or R 15 ;

R 9 is R 15 ;

each of R 10 , R 11 and R 12 , independently, is SR 14 , OR 14 , SR 15 , OR 15 , NR 14 R 15 , NR 15 R 15 , C(O)R 14 , C(O)R 15 , COOR 15 , OC(O)R 15 , C(O)C(O)R 15 , C(O)NR 14 R 15 , C(O)NR 15 R 15 , NR 15 C(O)R 14 , NR 15 C(O)R 15 , NR 15 C(O)NR 14 R 15 , NR 15 C(O)NR 15 R 15 , NR 15 C(O)C(O)R 15 , NR 15 (COOR 15 ), OC(O)NR 15 R 15 , S(O) 2 R 14 , S(O) 2 R 15 , S(O) 2 NR 14 R 15 , S(O) 2 NR 15 R 15 , NR 15 S(O) 2 NR 15 R 15 , NR 15 S(O) 2 R 14 , NR 15 S(O) 2 R 15 , NR 15 S(O) 2 NR 14 R 15 , NR 15 C(O)C(O)NR 14 R 15 , NR 15 C(O)C(O)NR 15 R 15 or R 15 ;

R 13 is SR 14 , OR 14 , SR 15 , OR 15 , NR 14 R 15 , NR 15 R 15 , C(O)R 14 , C(O)R 15 , OC(O)R 14 , OC(O)R 15 , COOR 14 , COOR 15 , C(O)NR 14 R 15 , C(O)NR 15 R 15 , NR 15 C(O)R 14 , NR 15 C(O)R 15 , C(O)C(O)R 15 , NR 15 C(O)NR 14 R 15 , NR 15 C(O)NR 15 R 15 , NR 15 C(O)C(O)R 15 , NR 15 (COOR 14 ), NR 15 (COOR 15 ), NR 15 C(O)C(O)NR 14 R 15 , NR 15 C(O)C(O)NR 15 R 15 , S(O) 2 R 14 , S(O) 2 R 15 , S(O) 2 NR 14 R 15 , S(O) 2 NR 15 R 15 , NR 15 S(O) 2 R 14 , NR 15 S(O) 2 R 15 , NR 15 S(O) 2 NR 14 R 15 or NR 15 S(O) 2 NR 15 R 15 ;

R 14 is a partially or fully saturated or fully unsaturated 5-8 membered monocyclic, 6-12 membered bicyclic, or 7-14 membered tricyclic ring system, the ring system formed of carbon atoms optionally including 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, the heteroatoms selected from O, N, or S, wherein 0, 1, 2 or 3 atoms of each ring is optionally substituted independently with 1-3 substituents of R 15 ; and

R 15 is H, halo, haloalkyl, haloalkoxyl, oxo, CN, OH, SH, NO 2 , NH 2 , acetyl, C 1-10 -alkyl, C 2-10 -alkenyl, C 2-10 -alkynyl, C 3-10 -cycloalkyl, C 4-10 -cycloalkenyl, C 1-10 -alkylamino-, C 1-10 -alkoxyl, C 1-10 -thioalkoxyl or a saturated or partially or fully unsaturated 5-8 membered monocyclic, 6-12 membered bicyclic, or 7-14 membered tricyclic ring system, said ring system formed of carbon atoms optionally including 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S, wherein each of the C 1-10 -alkyl, C 2-10 -alkenyl, C 2-10 -alkynyl, C 3-10 -cycloalkyl, C 4-10 -cycloalkenyl, C 1-10 -alkylamino-, C 1-10 -dialkylamino-, C 1-10 -alkoxyl, C 1-10 -thioalkoxyl and ring of said ring system is optionally substituted independently with 1-3 substituents of halo, haloalkyl, CN, NO 2 , NH 2 , OH, oxo, methyl, methoxyl, ethyl, ethoxyl, propyl, propoxyl, isopropyl, cyclopropyl, butyl, isobutyl, tert-butyl, methylamino, dimethylamino, ethylamino, diethylamino, propylamino, isopropylamino, dipropylamino, diisopropylamino, benzyl or phenyl;

provided that (1) no more than one of D 1 and D 2 is N, and (2) each of L 1 and L 2 is, independently, bound to the first ring of B.

2. The compound of claim 1 , wherein D 1 is N, D 2 is CR 12 .

3. The compound of claim 1 , wherein D 2 is N and D 1 is CR 11 .

4. The compound of claim 1 , wherein

C 1 is CR 19 ;

C 2 is N; and

R 2 is H, halo, NO 2 , CN, C 1-10 alkyl or C 1-10 alkoxyl.

5. The compound of claim 1 , wherein

L 1 is NR 15 , O, S, S(O) or SO 2 ; and

R 2 is H, halo, NO 2 , CN, C 1-10 alkyl or C 1-10 alkoxyl.

6. The compound of claim 1 , wherein

L 1 is NR 15 , O or S;

L 2 is NR 15 wherein R 15 is H or C 1-3 alkyl;

R 2 is H, halo, NO 2 , CN, C 1-10 alkyl or C 1-10 alkoxyl;

each of R 3 , R 4 and R 9 , independently, is H; and

C 1 is CR 10 .

7. The compound of claim 1 , wherein the first monocyclic ring of B is phenyl, pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, triazinyl, thiophenyl, furyl, pyrrolyl, pyrazolyl, imidazolyl, triazolyl, tetrazolyl, thiazolyl, thiadiazolyl, oxazolyl, oxadiazolyl, isoxazolyl, or isothiazolyl; and

where the first monocyclic ring of B is a fully unsaturated 6-membered ring, then L 1 and L 2 , together, are para to one another on said first monocyclic ring of B.

8. The compound of claim 7 , wherein R 6 and R 7 taken together with the carbon atoms to which they are attached form a partially or fully unsaturated 5- or 6-membered ring of carbon atoms optionally including 1-3 nitrogen atoms, and the ring optionally substituted independently with 1-4 substituents of R 13 , R 14 or R 15 .

9. The compound of claim 8 , wherein A is

wherein A 1 is N and A 2 is NH, O or S.

10. The compound of claim 9 , wherein R 6 and R 7 taken together with the carbon atoms to which they are attached form a phenyl ring optionally substituted independently with 1-3 substituents of R 15 .

11. The compound of claim 1 , wherein A is

12. The compound of claim 1 , wherein A is

13. A compound of Formula II:

or a stereoisomer or pharmaceutically acceptable salt thereof, wherein

A 1 is N or CR 8 ;

A 2 is NR 9 , O or S;

A′ is a fused ring selected from phenyl, pyridine, pyrimidine and pyridazine, each of which is optionally substituted independently with 1-3 substituents of R 13 , R 14 or R 15 ;

each of B 1 , B 2 , B 3 and B 4 , independently, is N or CR 5 , provided that no more than two of B 1 , B 2 , B 3 and B 4 is N;

alternatively, each of B 1 and B 2 , independently, is CR 5 , wherein both R 5 groups taken together with the carbon atoms to which they are attached form a 5- or 6-membered ring of carbon atoms, said ring optionally including 1-3 heteroatoms selected from N, O or S, and optionally substituted with 1-4 substituents of R 13 , R 14 or R 15 ;

C 1 is N or CR 10 ;

D 1 is N or CR 11 ;

D 2 is N or CR 12 ;

L 1 is NR 3 , O, S or CR 3 R 3 ;

L 2 is NR 3 , O, S or CR 3 R 3 ;

R 1 is OR 14 , SR 14 , OR 15 , SR 15 , NR 14 R 15 , NR 15 R 15 , (CHR 15 ) n R 14 , (CHR 15 ) n R 15 or R 15 , wherein n is 0, 1, 2, 3 or 4;

alternatively R 1 and R 11 taken together with the carbon atoms to which they are attached form a partially or fully unsaturated 5- or 6-membered ring of carbon atoms optionally including 1-3 heteroatoms selected from O, N and S, and the ring optionally substituted independently with 1-4 substituents of R 15 , SR 14 , OR 14 , SR 15 , OR 15 , OC(O)R 15 , COOR 15 , C(O)R 15 , C(O)NR 15 R 15 , NR 14 R 15 or NR 15 R 15 ;

R 2 is SR 14 , OR 14 , SR 15 , OR 15 , NR 14 R 15 , NR 15 R 15 , C(O)R 14 , C(O)R 15 , COOR 15 , OC(O)R 15 , C(O)C(O)R 15 , C(O)NR 14 R 15 , C(O)NR 15 R 15 , NR 15 C(O)R 14 , NR 15 C(O)R 15 , NR 15 C(O)NR 14 R 15 , NR 15 C(O)NR 15 R 15 , NR 15 C(O)C(O)R 15 , NR 15 (COOR 15 ), OC(O)NR 15 R 15 , S(O) 2 R 14 , S(O) 2 R 15 , S(O) 2 NR 14 R 15 , S(O) 2 NR 15 R 15 , NR 15 S(O) 2 NR 14 R 15 , NR 15 S(O) 2 NR 15 R 15 , NR 15 S(O) 2 R 14 , NR 15 S(O) 2 R 15 or R 15 ;

each of R 3 and R 4 , independently, is SR 14 , OR 14 , SR 15 , OR 15 , NR 14 R 15 , NR 15 R 15 , C(O)R 14 , C(O)R 15 or R 15 ;

alternatively, either of R 3 or R 4 , independently, taken together with R 10 and the carbon atoms to which they are attached form a partially or fully unsaturated 5- or 6-membered ring of carbon atoms optionally including 1-3 heteroatoms selected from O, N, or S, and the ring optionally substituted independently with 1-4 substituents of R 13 , R 14 or R 15 ;

each R 5 is, independently, is SR 14 , OR 14 , SR 15 , OR 15 , NR 14 R 15 , NR 15 R 15 , C(O)R 14 , C(O)R 15 , COOR 15 , OC(O)R 15 , C(O)C(O)R 15 , C(O)NR 14 R 15 , C(O)NR 15 R 15 , NR 15 C(O)R 14 , NR 15 C(O)R 15 , NR 15 C(O)NR 14 R 15 , NR 15 C(O)NR 15 R 15 , NR 15 C(O)C(O)R 15 , NR 15 (COOR 15 ), OC(O)NR 15 R 15 , S(O) 2 R 14 , S(O) 2 R 15 , S(O) 2 NR 14 R 15 , S(O) 2 NR 15 R 15 , NR 15 S(O) 2 NR 15 R 15 , NR 15 S(O) 2 R 14 , NR 15 S(O) 2 R 15 , NR 15 S(O) 2 NR 14 R 15 , NR 15 C(O)C(O)NR 14 R 15 , NR 15 C(O)C(O)NR 15 R 15 or R 15 ;

R 8 is SR 14 , OR 14 , SR 15 , OR 15 , NR 14 R 15 , NR 15 R 15 , C(O)R 14 , C(O)R 15 or R 15 ;

R 9 is H, halo, haloalkyl, haloalkoxyl, oxo, CN, OH, SH, NO 2 , NH 2 , acetyl, C 1-10 -alkyl, C 1-10 -alkoxyl, C 2-10 -alkenyl, C 2-10 -alkynyl or a saturated or partially or fully unsaturated 5-8 membered monocyclic, 6-12 membered bicyclic, or 7-14 membered tricyclic ring system, said ring system formed of carbon atoms optionally including 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S, wherein each of the C 1-10 -alkyl, C 1-10 -alkoxyl, C 2-10 -alkenyl, C 2-10 -alkynyl, and ring of said ring system is optionally substituted independently with 1-3 substituents of halo, haloalkyl, CN, NO 2 , NH 2 , OH, oxo, methyl, methoxyl, ethyl, ethoxyl, propyl, propoxyl, isopropyl, cyclopropyl, butyl, isobutyl, tert-butyl, methylamino, dimethylamino, ethylamino, diethylamino, propylamino, isopropylamino, dipropylamino, diisopropylamino, benzyl or phenyl;

each of R 10 , R 11 and R 12 , independently, is SR 14 , OR 14 , SR 15 , OR 15 , NR 14 R 15 , NR 15 R 15 , C(O)R 14 , C(O)R 15 or R 15 ;

R 13 is SR 14 , OR 14 , SR 15 , OR 15 , NR 14 R 15 , NR 15 R 15 , C(O)R 14 , C(O)R 15 , OC(O)R 14 , OC(O)R 15 , COOR 14 , COOR 15 , C(O)NR 14 R 15 , C(O)NR 15 R 15 , NR 15 C(O)R 14 , NR 15 C(O)R 15 , C(O)C(O)R 15 , NR 15 C(O)NR 14 R 15 , NR 15 C(O)NR 15 R 15 , NR 15 C(O)C(O)R 15 , NR 15 (COOR 14 ), NR 15 (COOR 15 ), NR 15 C(O)C(O)NR 14 R 15 , NR 15 C(O)C(O)NR 15 R 15 , S(O) 2 R 14 , S(O) 2 R 15 , S(O) 2 NR 14 R 15 , S(O) 2 NR 15 R 15 , NR 15 S(O) 2 R 14 , NR 15 S(O) 2 R 15 , NR 15 S(O) 2 NR 14 R 15 or NR 15 S(O) 2 NR 15 R 15 ;

R 14 is a partially or fully saturated or fully unsaturated 5-8 membered monocyclic, 6-12 membered bicyclic, or 7-14 membered tricyclic ring system, the ring system formed of carbon atoms optionally including 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, the heteroatoms selected from O, N, or S, wherein 0, 1, 2 or 3 atoms of each ring is optionally substituted independently with 1-3 substituents of R 15 ; and

R 15 is H, halo, haloalkyl, haloalkoxyl, oxo, CN, OH, SH, NO 2 , NH 2 , acetyl, C 1-10 -alkyl, C 2-10 -alkenyl, C 2-10 -alkynyl, C 3-10 -cycloalkyl, C 4-10 -cycloalkenyl, C 1-10 -alkylamino-, C 1-10 -dialkylamino-, C 1-10 -alkoxyl, C 1-10 -thioalkoxyl or a saturated or partially or fully unsaturated 5-8 membered monocyclic, 6-12 membered bicyclic, or 7-14 membered tricyclic ring system, said ring system formed of carbon atoms optionally including 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S, wherein each of the C 1-10 -alkyl, C 2-10 -alkenyl, C 2-10 -alkynyl, C 3-10 -cycloalkyl, C 4-10 -cycloalkenyl, C 1-10 -alkylamino-, C 1-10 -dialkylamino-, C 1-10 -alkoxyl, C 1-10 -thioalkoxyl and ring of said ring system is optionally substituted independently with 1-3 substituents of halo, haloalkyl, CN, NO 2 , NH 2 , OH, oxo, methyl, methoxyl, ethyl, ethoxyl, propyl, propoxyl, isopropyl, cyclopropyl, butyl, isobutyl, tert-butyl, methylamino, dimethylamino, ethylamino, diethylamino, propylamino, isopropylamino, dipropylamino, diisopropylamino, benzyl or phenyl;

provided that no more than one of D 1 and D 2 is N.

14. The compound of claim 13 , wherein

A 1 is N;

A 2 is NR 9 , O or S;

each of B 1 , B 2 , B 3 and B 4 , independently, is CR 5 ;

C 1 is CR 10 ;

D 1 is N or CR 11 ;

D 2 is N or CR 12 ;

L 1 is NH, O or S;

L 2 is NH;

R 1 is H, halo, haloalkyl, NO 2 , NH 2 , acetyl, C 1-10 -alkyl, C 2-10 -alkenyl, C 2-10 -alkynyl, C 3-10 -cycloalkyl, C 1-10 -alkylamino-, C 1-10 -dialkylamino-, C 1-10 -alkoxyl, C 1-10 -thioalkoxyl, NHR 14 , NHR 15 , OR 15 , SR 15 or CH 2 R 15 ;

R 2 is H, halo, NO 2 , CN, C 1-10 alkyl or C 1-10 alkoxyl;

each of R 3 and R 4 , independently, is SR 15 , OR 15 , NR 14 R 15 , NR 15 R 15 , C(O)R 14 , C(O)R 15 or R 15 ;

each R 5 is, independently, is SR 15 , OR 15 , NR 15 R 15 , C(O)R 15 , C(O)NR 15 R 15 , NR 15 C(O)R 15 , NR 15 C(O)NR 15 R 15 , NR 15 (COOR 15 ), S(O) 2 R 15 , S(O) 2 NR 15 R 15 , NR 15 S(O) 2 NR 15 R 15 , NR 15 S(O) 2 R 15 , NR 15 C(O)C(O)NR 14 R 15 or R 15 ; and

R 8 is SR 15 , OR 15 , NR 15 R 15 , C(O)R 15 or R 15 ;

R 9 is H, CN, acetyl or C 1-10 -alkyl; and

each of R 10 , R 11 and R 12 , independently, is SR 15 , OR 15 , NR 15 R 15 , C(O)R 14 , C(O)R 15 or R 15 ;

provided that no more than one of D 1 and D 2 is N.

15. The compound of claim 13 wherein,

R 1 is NR 14 R 15 , NR 15 R 15 , (CHR 15 ) n R 14 , (CHR 15 ) n R 15 or R 15 ; alternatively R 1 and R 11 taken together with the carbon atoms to which they are attached form a partially or fully unsaturated 5- or 6-membered ring of carbon atoms optionally including 1-3 heteroatoms selected from O, N and S, and the ring optionally substituted independently with 1-4 substituents of R 15 ;

R 2 is H, halo, haloalkyl, CN, NO 2 , NH 2 , OH, methyl, methoxyl, ethyl, ethoxyl, propyl, propoxyl, isopropyl, cyclopropyl, butyl, isobutyl, tert-butyl, methylamino, dimethylamino, ethylamino, diethylamino, propylamino, isopropylamino, dipropylamino, diisopropylamino, benzyl or phenyl;

each of R 3 and R 4 , independently, is H, halo, haloalkyl, CN, NO 2 , NH 2 , OH, methyl, methoxyl, ethyl, ethoxyl, propyl, propoxyl, isopropyl, cyclopropyl, butyl, isobutyl, tert-butyl, methylamino, dimethylamino, ethylamino, diethylamino, propylamino, isopropylamino, dipropylamino, diisopropylamino, benzyl or phenyl;

each R 5 is, independently, is H, halo, haloalkyl, CN, NO 2 , NH 2 , OH, methyl, methoxyl, ethyl, ethoxyl, propyl, propoxyl, isopropyl, cyclopropyl, butyl, isobutyl, tert-butyl, methylamino, dimethylamino, ethylamino, diethylamino, propylamino, isopropylamino, dipropylamino or diisopropylamino;

R 8 is H, halo, haloalkyl, CN, NO 2 , NH 2 , OH, methyl, methoxyl, ethyl, ethoxyl, propyl, propoxyl, isopropyl, cyclopropyl, butyl, isobutyl, tert-butyl, methylamino, dimethylamino, ethylamino, diethylamino, propylamino, isopropylamino, dipropylamino or diisopropylamino;

R 9 is H or C 1-10 -alkyl; and

each of R 10 , R 11 and R 12 , independently, is H, halo, haloalkyl, CN, NO 2 , NH 2 , OH, methyl, methoxyl, ethyl, ethoxyl, propyl, propoxyl, isopropyl, cyclopropyl, butyl, isobutyl, tert-butyl, methylamino, dimethylamino, ethylamino, diethylamino, propylamino, isopropylamino, dipropylamino or diisopropylamino.

16. A compound of Formula III:

or a stereoisomer or pharmaceutically acceptable salt thereof, wherein

A 1 is N or CR 8 ;

A 2 is NR 9 , O or S;

each of B 1 , B 2 , B 3 and B 4 , independently, is N or CR 5 , provided that no more than two of B 1 , B 2 , B 3 and B 4 is N;

C 1 is CR 10 ;

L 1 is O, S, C(O), S(O), SO 2 or CR 3 R 3 ;

L 2 is NR 3 , O, S or CR 3 R 3 ;

R 1 is OR 14 , SR 14 , OR 15 , SR 15 , NR 14 R 15 , NR 15 R 15 , (CHR 15 ) n R 14 , (CHR 15 ) n R 15 or R 15 ;

R 2 is SR 14 , OR 14 , SR 15 , OR 15 , NR 14 R 15 , NR 15 R 15 , C(O)R 14 , C(O)R 15 , COOR 15 , OC(O)R 15 , C(O)C(O)R 15 , C(O)NR 14 R 15 , C(O)NR 15 R 15 , NR 15 C(O)R 14 , NR 15 C(O)R 15 , NR 15 C(O)NR 14 R 15 , NR 15 C(O)NR 15 R 15 , NR 15 C(O)C(O)R 15 , NR 15 (COOR 15 ), OC(O)NR 15 R 15 , S(O) 2 R 14 , S(O) 2 R 15 , S(O) 2 NR 14 R 15 , S(O) 2 NR 15 R 15 , NR 15 S(O) 2 NR 14 R 15 , NR 15 S(O) 2 NR 15 R 15 , NR 15 S(O) 2 R 14 , NR 15 S(O) 2 R 15 or R 15 ;

each of R 3 and R 4 , independently, is SR 14 , OR 14 , SR 15 , OR 15 , NR 14 R 15 , NR 15 R 15 , C(O)R 14 , C(O)R 15 or R 15 ;

alternatively, either of R 3 or R 4 , independently, taken together with R 10 and the carbon atoms to which they are attached form a partially or fully unsaturated 5- or 6-membered ring of carbon atoms optionally including 1-3 heteroatoms selected from O, N, or S, and the ring optionally substituted independently with 1-4 substituents of R 13 , R 14 or R 15 ;

each R 5 is, independently, is SR 14 , OR 14 , SR 15 , OR 15 , NR 14 R 15 , NR 15 R 15 , C(O)R 14 , NR 15 C(O)R 15 , COOR 15 , OC(O)R 15 , C(O)C(O)R 15 , C(O)NR 14 R 15 , C(O)NR 15 R 15 , NR 15 C(O)R 14 , NR 15 C(O)R 15 , NR 15 C(O)NR 14 R 15 , NR 15 C(O)NR 15 R 15 , NR 15 C(O)C(O)R 15 , NR 15 (COOR 15 ), OC(O)NR 15 R 15 , S(O) 2 R 14 , S(O) 2 R 15 , S(O) 2 NR 14 R 15 , S(O) 2 NR 15 R 15 , NR 15 S(O) 2 NR 15 R 15 , NR 15 S(O) 2 R 14 , NR 15 S(O) 2 R 15 , NR 15 S(O) 2 NR 14 R 15 , NR 15 , C(O)C(O)NR 14 R 15 , NR 15 C(O)C(O)NR 15 R 15 or R 15 ;

each of R 6 , R 7 and R 8 , independently, is R 13 , R 14 or R 15 ;

alternatively, R 6 and R 7 taken together with the carbon atoms to which they are attached form a partially or fully unsaturated 5- or 6-membered ring of carbon atoms optionally including 1-3 heteroatoms selected from O, N, or S, and the ring optionally substituted independently with 1-4 substituents of R 13 , R 14 or R 15 ;

R 9 is R 15 ;

each of R 10 , R 11 and R 12 , independently, is SR 14 , OR 14 , SR 15 , OR 15 , NR 14 R 15 , NR 15 R 15 , C(O)R 14 , C(O)R 15 or R 15 ;

R 13 is SR 14 , OR 14 , SR 15 , OR 15 , NR 14 R 15 , NR 15 R 15 , C(O)R 14 , C(O)R 15 , OC(O)R 14 , OC(O)R 15 , COOR 14 , COOR 15 , C(O)NR 14 R 15 , C(O)NR 15 R 15 , NR 15 C(O)R 14 , NR 15 C(O)R 15 , C(O)C(O)R 15 , NR 15 C(O)NR 14 R 15 , NR 15 C(O)NR 15 R 15 , NR 15 C(O)C(O)R 15 , NR 15 (COOR 14 ), NR 15 (COOR 15 ), NR 15 C(O)C(O)NR 14 R 15 , NR 15 C(O)C(O)NR 15 R 15 , S(O) 2 R 14 , S(O) 2 R 15 , S(O) 2 NR 14 R 15 , S(O) 2 NR 15 R 15 , NR 15 S(O) 2 R 14 , NR 15 S(O) 2 R 15 , NR 15 S(O) 2 NR 14 R 15 or NR 15 S(O) 2 NR 15 R 15 ;

R 14 is a partially or fully saturated or fully unsaturated 5-8 membered monocyclic, 6-12 membered bicyclic, or 7-14 membered tricyclic ring system, the ring system formed of carbon atoms optionally including 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, the heteroatoms selected from O, N, or S, wherein 0, 1, 2 or 3 atoms of each ring is optionally substituted independently with 1-3 substituents of R 15 ;

R 15 is H, halo, haloalkyl, haloalkoxyl, oxo, CN, OH, SH, NO 2 , NH 2 , acetyl, C 1-10 -alkyl, C 2-10 -alkenyl, C 2-10 -alkynyl, C 3-10 -cycloalkyl, C 4-10 -cycloalkenyl, C 1-10 -alkylamino-, C 1-10 -dialkylamino-, C 1-10 -alkoxyl, C 1-10 -thioalkoxyl or a saturated or partially or fully unsaturated 5-8 membered monocyclic, 6-12 membered bicyclic, or 7-14 membered tricyclic ring system, said ring system formed of carbon atoms optionally including 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S, wherein each of the C 1-10 -alkyl, C 2-10 -alkenyl, C 2-10 -alkynyl, C 3-10 -cycloalkyl, C 4-10 -cycloalkenyl, C 1-10 -alkylamino-, C 1-10 -dialkylamino-, C 1-10 -alkoxyl, C 1-10 -thioalkoxyl and ring of said ring system is optionally substituted independently with 1-3 substituents of halo, haloalkyl, CN, NO 2 , NH 2 , OH, oxo, methyl, methoxyl, ethyl, ethoxyl, propyl, propoxyl, isopropyl, cyclopropyl, butyl, isobutyl, tert-butyl, methylamino, dimethylamino, ethylamino, diethylamino, propylamino, isopropylamino, dipropylamino, diisopropylamino, benzyl or phenyl; and

n is 0, 1, 2, 3 or 4.

17. A compound or a stereoisomer or pharmaceutically acceptable salt thereof, selected from:

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-5-(trifluoromethyl)-1H-benzimidazol-2-amine;

N-(4-((3-(4-(methylamino)-1,3,5-triazin-2-yl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1,3-benzoxazol-2-amine;

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1,3-benzothiazol-2-amine;

5,6-difluoro-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

4-methyl-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-((2-(4-morpholinyl)ethyl)amino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

6-chloro-5-fluoro-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-(methylsulfanyl)-4-pyrimidinyl)-2-pyridinyl) oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

N˜1˜-(4-(2-((4-(1H-benzimidazol-2-ylamino)-1-naphthalenyl) oxy)-3-pyridinyl)-2-pyrimidinyl)-N˜2˜,N˜2˜-dimethyl-1,2-ethanediamine;

N˜1˜-(4-(2-((4-(1H-benzimidazol-2-ylamino)-1-naphthalenyl) oxy)-3-pyridinyl)-2-pyrimidinyl)-N˜3˜,N˜3˜-dimethyl-1,3-propanediamine;

N-(4-((3-(2-(methylsulfonyl)-4-pyrimidinyl)-2-pyridinyl) oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

5,7-difluoro-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

N-(1-(4-(2-((4-(1H-benzimidazol-2-ylamino)-1-naphthalenyl) oxy)-3-pyridinyl)-2-pyrimidinyl)-N-4-,N-4-dimethyl-1,4-butanediamine;

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-5,7-bis(trifluoromethyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-3H-imidazo[4,5-b]pyridin-2-amine;

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-3H-imidazo[4,5-c]pyridin-2-amine;

1-(3-(dimethylamino)propyl)-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

1-(2-(dimethylamino)ethyl)-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl) oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-((3-(1-pyrrolidinyl)propyl)amino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

N-(3-methyl-4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

N-(3,5-dichloro-4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

N-1H-benzimidazol-2-yl-8-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-5-quinolinamine;

4,5-difluoro-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

6,7-difluoro-N-(6-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-3-pyridinyl)-1H-benzimidazol-2-amine;

N-(4-((2-(2-(methylamino)-4-pyrimidinyl)phenyl)oxy)phenyl)-1H-benzimidazol-2-amine;

6,7-difluoro-N-(4-((2-(2-(methylamino)-4-pyrimidinyl)phenyl) oxy)phenyl)-1H-benzimidazol-2-amine;

2-((4-(1H-benzimidazol-2-ylamino) phenyl)oxy)-N-methyl-3,4′-bipyridin-2′-amine;

2-((4-((6,7-difluoro-1H-benzimidazol-2-yl)amino)phenyl)oxy)-N-methyl-3,4′-bipyridin-2′-amine;

N-(4-((3-(2-amino-4-pyrimidinyl)-2-pyridinyl)oxy)-3-methyl-1-naphthalenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-((2-(1-methyl-2-pyrrolidinyl)ethyl)amino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

5,7-dimethyl-N-(3-methyl-4-((3-(4-pyrimidinyl)-2-pyridinyl) oxy)phenyl)-1,3-benzoxazol-2-amine;

6-methyl-N-(3-methyl-4-((3-(4-pyrimidinyl)-2-pyridinyl) oxy)phenyl)-1,3-benzoxazol-2-amine;

5-methyl-N-(3-methyl-4-((3-(4-pyrimidinyl)-2-pyridinyl) oxy)phenyl)-1,3-benzoxazol-2-amine;

4-methyl-N-(3-methyl-4-((3-(4-pyrimidinyl)-2-pyridinyl) oxy)phenyl)-1,3-benzoxazol-2-amine;

N-(4-((3-(2-(((1-ethyl-4-piperidinyl)methyl)amino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-((1-methyl-4-piperidinyl)amino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine

4,5-difluoro-N-(4-((3-(1H-pyrazol-4-yl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(1H-pyrazol-4-yl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-amino-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-4,5-difluoro-1H-benzimidazol-2-amine;

N-(6-((3-(2-amino-4-pyrimidinyl)-2-pyridinyl)oxy)-3-pyridinyl)-6,7-difluoro-1H-benzimidazol-2-amine;

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1,3-benzoxazol-2-amine;

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

N-(3-methyl-4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1,3-benzoxazol-2-amine;

N-(3-methyl-4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1,3-benzothiazol-2-amine;

5-methyl-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-5-(trifluoromethyl)-1H-benzimidazol-2-amine;

5-methyl-N-(3-methyl-4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

N-(3-methyl-4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-5-(trifluoromethyl)-1H-benzimidazol-2-amine;

1-methyl-N-(3-methyl-4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

1-methyl-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

1-methyl-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-5-(trifluoromethyl)-1H-benzimidazol-2-amine;

5,6-difluoro-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

5-(1,1-dimethylethyl)-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

6-chloro-5-fluoro-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

4-methyl-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

5-fluoro-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

4-methyl-N-(3-methyl-4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

5-fluoro-N-(3-methyl-4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

5,6-difluoro-N-(3-methyl-4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

6-chloro-5-fluoro-N-(3-methyl-4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

N-(2-methyl-4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

N-(2,3-dimethyl-4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

5,6-dimethyl-N-(4-(3-(2-(methylamino)pyramidin-4-yl)pyridin-2-yloxy)phenyl)-1H-benzo[d]imidazol-2-amine;

4,6-difluoro-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

4,5-dimethyl-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

5-fluoro-N-(4-((3-(2-((3-(4-morpholinyl)propyl)amino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

5,6-dichloro-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-4,6-bis(trifluoromethyl)-1H-benzimidazol-2-amine;

5-chloro-6-methyl-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

5-fluoro-N-(4-((3-(2-((4-(4-methyl-1-piperazinyl)phenyl)amino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-5-(4-methyl-1-piperazinyl)-1H-benzimidazol-2-amine;

N′-(4-(2-((4-((5,6-difluoro-1H-benzimidazol-2-yl)amino)phenyl)oxy)-3-pyridinyl)-2-pyrimidinyl)-N,N-dimethyl-1,3-propanediamine;

4,5-difluoro-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-((3-(1-piperidinyl)propyl)amino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

N′-(4-(2-((4-(1H-benzimidazol-2-ylamino)-1-naphthalenyl) oxy)-3-pyridinyl)-2-pyrimidinyl)-N,N,2,2-tetramethyl-1,3-propanediamine;

5,6-difluoro-N-(4-((3-(1H-pyrrolo[2,3-b]pyridin-4-yl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-((3-(1H-1,2,3-triazol-1-yl)propyl)amino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

5,6-difluoro-N-(4-((3-(2-((3-(4-thiomorpholinyl)propyl)amino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

N′-(4-(2-((4-((5,6-difluoro-1H-benzimidazol-2-yl)amino) phenyl)oxy)-3-pyridinyl)-2-pyrimidinyl)-N,N-dimethyl-1,4-butanediamine;

2,2′-((3-((4-(2-((4-((5,6-difluoro-1H-benzimidazol-2-yl)amino)phenyl)oxy)-3-pyridinyl)-2-pyrimidinyl)amino) propyl)imino)diethanol;

N′-(4-(2-((4-((5,6-difluoro-1H-benzimidazol-2-yl)amino) phenyl)oxy)-3-pyridinyl)-2-pyrimidinyl)-N,N-dimethyl-1,5-pentanediamine;

N′-(4-(2-((4-((5,6-difluoro-1H-benzimidazol-2-yl)amino) phenyl)oxy)-3-pyridinyl)-2-pyrimidinyl)-N,N-dimethyl-1,6-hexanediamine;

5,6-difluoro-N-(4-((3-(2-((3-(4-morpholinyl)propyl)amino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

4,5,6-trifluoro-N-(4-(3-(2-(methylamino)pyrimidin-4-yl)pyridin-2-yloxy)phenyl)-1H-benzo[d]imidazol-2-amine;

N-(4-(3-(2-(methylamino)pyrimidin-4-yl)pyridin-2-yloxy)phenyl)-1H-thieno[3,4-d]imidazol-2-amine;

N-(4-((3-(1H-pyrrolo[2,3-b]pyridin-4-yl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)thio) phenyl)-1H-benzimidazol-2-amine;

4,5-difluoro-N-(4-((3-(1H-pyrrolo[2,3-b]pyridin-4-yl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

4,5-difluoro-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)thio)phenyl)-1H-benzimidazol-2-amine;

4,5-difluoro-N-(4-((3-(2-((4-(4-methyl-1-piperazinyl)phenyl)amino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

4,5-difluoro-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-3-(methyloxy)phenyl)-1H-benzimidazol-2-amine

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-3-(methyloxy)phenyl)-1H-benzimidazol-2-amine;

4,5-difluoro-N-(3-methyl-4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

4,5,6,7-tetrafluoro-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

4,5-difluoro-N-(2-fluoro-4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-1-phenyl-1H-benzimidazol-2-amine;

N-(3-chloro-4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-4,5-difluoro-1H-benzimidazol-2-amine;

4-(2-((4-((4-methyl-1-phenyl-1H-pyrazol-3-yl)amino)phenyl) oxy)-3-pyridinyl)-2-pyrimidinamine;

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-5-(trifluoromethyl)-1H-benzimidazol-2-amine;

N-(4-((3-(4-(methylamino)-1,3,5-triazin-2-yl)-2-pyridinyl) oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1,3-benzoxazol-2-amine;

N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1,3-benzothiazol-2-amine;

5,6-difluoro-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

4-methyl-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

N-(4-((3-(2-((2-(4-morpholinyl)ethyl)amino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine;

6-chloro-5-fluoro-N-(4-((3-(2-(methylamino)-4-pyrimidinyl)-2-pyridinyl)oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine; and

N-(4-((3-(2-(methylsulfanyl)-4-pyrimidinyl)-2-pyridinyl) oxy)-1-naphthalenyl)-1H-benzimidazol-2-amine.

18. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and the compound of claim 1 .

19. A method of treating breast cancer or rheumatoid arthritis in a subject, the method comprising administering to the subject an effective dosage amount of the compound of claim 1 .

20. A method of making a compound of claim 1 , the method comprising the step of reacting compound of Formula A

with a compound of Formula B

wherein A, B, C 1 , C 2 , D, L 1 , L 2 and R 3-4 are defined in claim 1 and X is a halogen, to make a compound of Formula I.

21. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and the compound of claim 13 .

22. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and the compound of claim 16 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 31, 2007
From: CEE, VICTOR J.; DEAK, HOLLY L.; GEUNS-MEYER, STEPHANIE D.; HODOUS, BRIAN L.; NGUYEN, HANH NHO; OLIVIERI, PHILIP R.; PATEL, VINOD F.; ROMERO, KARINA
To: AMGEN INC.
Reel/Frame 019363/0196 →
Continuity (2)
Provisional Application 6077650700 · Feb 24, 2006
Related Publication 20070213325A1 · Sep 13, 2007