2-aminopyridine kinase inhibitors
2-Aminopyridine compounds having the structure of Formula I, and pharmaceutically acceptable salts of these compounds. Compounds of Formula I inhibit the activity of tyrosine kinase enzymes in animals, including humans, and are useful in the treatment and/or prevention of various diseases and conditions. In particular, compounds disclosed herein are inhibitors of kinases, in particular, but not limited to, KDR, Tie-2, Flt3, FGFR3, Ab1, Aurora A, c-Src, IGF-1R, ALK, c-MET, RON, PAK1, PAK2, and TAK1, and can be used in the treatment of proliferative diseases, such as, but not limited to, cancer. The present invention is also directed to a pharmaceutical composition comprising a therapeutically effective amount of a compound of Formula I, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. The present invention is further directed to a method of treating a patient having a condition which is mediated by protein kinase activity by administering to the patient a therapeutically effective amount of the above-mentioned pharmaceutical composition.
1. A compound of Formula I, or a pharmaceutically acceptable salt thereof,
wherein:
R1 is isoquinolin-3-yl or 1,2,3,4-tetrahydroisoquinolin-2-yl, either of which is optionally substituted with one to four independent R3 groups;
X is pyrazolyl, pyridyl, thiazolyl, imidazolyl, furyl, thienyl, pyrrolyl, indolyl, indazolyl, or tetrahydropyridyl;
R2 is H, halogen, CN, alkyl, cycloalkyl, bicycloalkyl, hydroxy, hydroxyalkyl, alkoxy, aryloxy, amino, aminoalkyl, alkylamino, alkylsulfonyl, C(═O)R4, C(═O)OR4, C(═O)NR5R6, NR7C(═O)R4, NR7C(═O)OR4, NR7C(═O)NR5R6, NR7S(═O) 2 R4, NR7S(═O)R4, aryl, heterocyclyl, heterobicycloalkyl, heterospiroalkyl, heteroaryl, -alkyl-C(═O)R4, -alkyl-C(═O)OR4, -alkyl-C(═O)NR5R6, -alkyl-NR7C(═O)R4, -alkyl-NR7C(═O)OR4, -alkyl-NR7C(═O)NR5R6, -alkyl-NR7SO 2 R4, -alkyl-NR7SOR4, aryl-alkyl, heterocyclyl-alkyl, or heteroaryl-alkyl, any of which is optionally substituted by one or more independent R3 groups;
R3 is H, halogen, CN, alkyl, cycloalkyl, alkenyl, alkynyl, hydroxy, hydroxyalkyl, alkoxy, aryloxy, amino, aminoalkyl, alkylamino, alkylsulfonyl, C(═O), C(═S), C(═O)R4, C(═O)OR4, C(═O)NR5R6, NR7C(═O)R4, NR7C(═O)OR4, NR7C(═O)NR5R6, NR7SO 2 R4, NR7SOR4, aryl, heterocyclyl, heteroaryl, -alkyl-C(═O)R4, -alkyl-C(═O)OR4, -alkyl-C(═O)NR5R6, -alkyl-NR7C(═O)R4, -alkyl-NR7C(═O)OR4, -alkyl-NR7C(═O)NR5R6, -alkyl-NR7SO 2 R4, -alkyl-NR7SOR4, aryl-alkyl, heterocyclyl-alkyl, or heteroaryl-alkyl, any of which is optionally further substituted by one or more independent R7 groups;
R4 is alkyl, cycloalkyl, alkenyl, alkynyl, hydroxy, hydroxyalkyl, alkoxy, aryloxy, amino, aminoalkyl, alkylamino, dialkylamino, alkylsulfonyl, aryl, heterocyclyl, heteroaryl, aryl-alkyl, heterocyclyl-alkyl, or heteroaryl-alkyl, any of which is optionally further substituted by one or more independent R7 groups;
R5 and R6 are each independently H, alkyl, cycloalkyl, or alkoxyalkyl, any of which is optionally substituted by one or more independent R7 groups; or R5 and R6 taken together with the atom that they are attached to form a 4-7 membered saturated or unsaturated heterocycle; wherein said heterocycle is optionally further substituted by one or more independent R7 groups;
R7 is H, halogen, alkyl, trifluoroalkyl, alkoxy, CN, cycloalkyl, alkoxyalkyl, aryl, hetaryl, or heterocyclyl;
n is 1.
2. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the compound of Formula I has the Formula Ia
3. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the compound has the Formula Iaa
wherein
Raa is H, alkoxy, or alkyl wherein alkoxy or alkyl is optionally further substituted with halogen; and Rab is H or F.
4. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the compound of has the Formula Iac
wherein
Rc is H or alkyl wherein alkyl is optionally further substituted with halogen.
5. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R2 is H, alkyl, cycloalkyl, bicycloalkyl, alkylsulfonyl, C(═O)NR5R6, aryl, heterocyclyl, heterobicycloalkyl, heterospiroalkyl, heteroaryl, -alkyl-C(═O)R4, -alkyl-C(═O)OR4, -alkyl-C(═O)NR5R6, -alkyl-NR7C(═O)R4, -alkyl-NR7C(═O)OR4, -alkyl-NR7C(═O)NR5R6, -alkyl-NR7SO 2 R4, -alkyl-NR7SOR4, aryl-alkyl, heterocyclyl-alkyl, or heteroaryl-alkyl, any of which is optionally further substituted by one or more independent R3 groups.
6. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R2 is H, alkyl, aryl, heterocyclyl, heterobicycloalkyl, heterospiroalkyl, or heteroaryl, any of which is optionally further substituted by one or more independent R3 groups.
7. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R2 is heterocyclyl or heterobicycloalkyl, any of which is optionally further substituted by one or more independent R3 groups.
8. A pharmaceutical composition comprising a compound claim 1 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.
9. A compound or a pharmaceutically acceptable salt thereof, which is selected from:
Structure
or