Heterocyclic compounds and uses as anticancer agents
The present disclosure provides pharmaceutical compounds, compositions and methods, especially as they are related to compositions and methods for the treatment of tumors and related diseases related to the dysregulation of kinase (such as EGFR (including HER), Alk, PDGFR, but not limited to) pathways.
1. A compound of Formula V:
wherein
X is CF 2 ;
R 3 and R 4 are independently hydrogen, C1-C6 alkyl, or —(CH 2 ) m N(R a ) 2 , wherein m is one to 6;
R 5 is hydrogen or C1-C6 alkyl;
R 6 is hydrogen or C1-C6 alkyl;
R 7 is hydrogen or C1-C6 alkyl;
R 24 and R 25 are independently selected from hydrogen, halogen, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 alkenyl, C1-C6 alkynyl, hydroxy, cyano, nitro, —C(O)R a , —OC(O)R a , —C(O)OR a , —C(O)N(R a ) 2 , sulfonyl, sulfonylamino, aminosulfonyl, amino, and substituted amino;
R 26 is hydrogen, C1-C6 alkyl, or substituted C1-C6 alkyl, wherein C1-C6 alkyl is substituted with halogen, hydroxy, cyano, nitro, sulfonyl, sulfonylamino, aminosulfonyl, amino, or substituted amino;
R 22 is selected from hydrogen, halogen, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 alkenyl, C1-C6 alkynyl, hydroxy, cyano, nitro, —C(O)R a , —OC(O)R a , —C(O)OR a , —C(O)N(R a ) 2 , sulfonyl, sulfonylamino, aminosulfonyl, amino, substituted amino acylamino, alkoxycarbonylamino, and aminocarbonylamino;
R 23 is selected from hydrogen, halogen, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 alkenyl, C1-C6 alkynyl, hydroxy, cyano, nitro, —C(O)R a , —OC(O)R a , —C(O)OR a , —C(O)N(R a ) 2 , sulfonyl, sulfonylamino, aminosulfonyl, amino, substituted amino acylamino, alkoxycarbonylamino, and aminocarbonylamino;
each R a is independently hydrogen or C1-C6 alkyl; and
Q is CH, CR 23 , or N;
or a pharmaceutically acceptable salt thereof.
2. The compound of claim 1 , wherein R 24 and R 25 are hydrogen.
3. The compound of claim 1 , wherein R 26 is hydrogen.
4. A pharmaceutical composition comprising a compound of claim 1 admixed with at least one pharmaceutically acceptable carrier or excipient.
5. A method to treat cancer, which comprises administering to a subject in need thereof an effective amount of a compound according to claim 1 .
6. A combination for treating cancer in a subject, which combination comprises an effective amount of a compound of claim 1 , or a pharmaceutically acceptable salt thereof, and an effective amount of a second prophylactic or therapeutic agent for treating and/or preventing cancer in a subject.
7. A method for treating cancer in a subject, which method comprises administering to a subject in need thereof an effective amount of the combination of claim 6 .
8. The compound according to claim 1 , wherein R 3 and R 4 are hydrogen.
9. The compound according to claim 1 , wherein R 5 , R 6 and R 22 are hydrogen.
10. The compound according to claim 1 , wherein R 7 is C1-3 alkyl.
11. The compound according to claim 1 , wherein R 7 is methyl.
12. The compound according to claim 1 , wherein R 23 is hydrogen.
13. The compound of claim 1 , wherein R 26 is C1-6 alkyl substituted with hydroxy.
14. The compound according to claim 1 , wherein Q is CH.
15. The compound according to claim 1 , wherein Q is CF.
16. The compound according to claim 1 , wherein Q is N.
17. A compound chosen from:
or a pharmaceutically acceptable salt thereof.
18. The compound according to claim 17 , wherein the compound is:
or a pharmaceutically acceptable salt thereof.
19. The compound according to claim 17 , wherein the compound is:
or a pharmaceutically acceptable salt thereof.
20. The compound according to claim 17 , wherein the compound is:
or a pharmaceutically acceptable salt thereof.