N,6-bis(aryl or heteroaryl)-1,3,5-triazine-2,4-diamine compounds as IDH2 mutants inhibitors for the treatment of cancer

1. A compound having Formula II:

or a pharmaceutically acceptable salt thereof, wherein:

ring A′ is selected from phenyl, pyrimidin-2-yl, pyrimidin-4-yl, pyrimidin-5-yl, oxazol-4-yl, isoxazol-3-yl, thiazol-2-yl, pyridin-3-yl and pyridin-2-yl, wherein ring A′ is optionally substituted with one or two substituents independently selected from 1-propenyl, -cyclopropyl-OH, chloro, fluoro, —CF 3 , —CHF 2 , —CH 3 , —CH 2 CH 3 , —CF 2 CH 3 , —S(O)CH 3 , —S(O) 2 CH 3 , —CH 2 OH, —CH(OH)CH 3 , —CH(OH)CF 3 , —OH, —OCH 3 , —OCH 2 CH 3 , —C(O)—NH 2 , —CH 2 NH 2 , —NH(CH 3 ), —CN and —N(CH 3 ) 2 ; and

ring B′ is selected from phenyl, pyridin-3-yl, pyridin-4-yl, pyridazin-4-yl, isoxazol-4-yl, isoxazol-3-yl, thiazol-5-yl, pyrimidin-5-yl and pyrazol-4-yl, wherein ring B′ is optionally substituted with one to two substituents independently selected from halo; —CN; —OH; C 1 -C 4 alkyl optionally substituted with halo, CN or —OH; —S(O) 2 —C 1 -C 4 alkyl; —S(O)—C 1 -C 4 alkyl; —S(O) 2 —NH—C 1 -C 4 alkyl; —S(O) 2 —NH—CH 2 —CF 3 ; —S(O) 2 —N(C 1 -C 4 alkyl) 2 ; —S(O) 2 -azetidin-1-yl; —O—C 1 -C 4 alkyl; —CH 2 —O—CH 3 , morpholin-4-yl, cyclopropyl, cyclopropyl-C 1 -C 4 alkyl, cyclopropyl-C 1 -C 4 alkoxy, cyclopropyl-CN, —S(O) 2 —NH-cyclopropyl; —S(O) 2 —NH—CH 2 -cyclopropyl; —C(O)—C 1 -C 4 alkyl, —C(O)—O—CH 3 ;

wherein:

a. ring A′ and ring B′ are not both an optionally substituted phenyl;

b. when ring A′ is unsubstituted pyridyl, then ring B′ is not phenyl optionally substituted with one to three groups independently selected from methyl, ethyl, t-butyl, methoxy, CH(OH)CH 3 , Cl, Br, and CF 3 ;

c. when ring A′ is oxazol-4-yl, isoxazol-3-yl, or thiazol-2-yl, then ring B′ is not phenyl optionally substituted with one to two groups independently selected from F, Cl, SO 2 CH 3 , C(O)OCH 3 , methyl, ethyl, t-butyl, methoxy, ethoxy, CF 3 , and OH;

d. the compound is not:

(1) N 2 -2-pyridinyl-6-(3-pyridinyl)-1,3,5-triazine-2,4-diamine;

(2) 6-(6-methoxy-3-pyridinyl)-N 2 -(4-methylphenyl)-1,3,5-triazine-2,4-diamine;

(3) 6-(2-methoxy-3-pyridinyl)-N 2 -(4-methylphenyl)-1,3,5-triazine-2,4-diamine;

(4) N 2 -(3-chlorophenyl)-6-(2-chloro-4-pyridinyl)-1,3,5-triazine-2,4-diamine;

(5) 3-[[4-[[4-amino-6-[(3-chlorophenyl)amino]-1,3,5-triazin-2-yl]-2-pyridinyl]amino]-1-propanol;

(6)N-[34[4-amino-6-(2-methyl-4-pyrimidinyl)-1,3,5-triazin-2-yl]amino]-4-methylphenyl]-N′-[4-chloro-3-(trifluoromethyl)phenyl]-urea;

(7) 2,6-bis[6-(2-amino-4-phenylamino-1,3,5-triazinyl)]pyridine; or

(8) 2,6-bis[6-(2-amino-4-phenylamino-1,3,5-triazinyl)]pyrazine.

2. The compound of claim 1 , wherein ring A′ is selected from 2-chlorophenyl, 2-fluorophenyl, 2-methoxyphenyl, 3-hydroxyphenyl, 3-amidophenyl, 3-methylsulfinylphenyl, 3-methyl sulfonylphenyl, 3-(1-methanol)phenyl, 3-methanaminephenyl, 3-methoxy-2-fluorophenyl, 5-methoxy-2-fluorophenyl, 3-hydroxy-2-fluorophenyl, 5-hydroxy-2-fluorophenyl, 5-hydroxy-3-fluorophenyl, 3-methanolphenyl, 3,5-dihydroxyphenyl, 3-trifluoromethyl-5-chlorophenyl, 3-(1-hydoxy-2,2,2-trifluoroethyl)phenyl, 3-(1-hydoxyethyl)phenyl, 3-(1-hydoxycyclopropyl)phenyl, 3-hydroxymethyl-5-phenol, pyridin-2-yl, 3-fluoropyridin-2-yl, 3-cyanopyridin-2-yl, 3,6-difluoropyridin-2-yl, 3-fluoro-6-methoxypyridin-2-yl, 3-fluoro-6-hydroxypyridin-2-yl, 3-fluoro-6-aminopyridin-2-yl, 4-fluoro-6-aminopyridin-2-yl, 6-propen-1-ylpyridin-2-yl, 6-methylaminopyridin-2-yl, 3-fluoro-6-trifluoromethylpyridin-2-yl, 4-chloro-6-aminopyridin-2-yl, 4-fluoro-6-aminopyridin-2-yl, 4-chloro-6-methoxypyridin-2-yl, 6-aminopyridin-3-yl, 2-methoxypyridin-3-yl, 6-aminopyridin-2-yl, 6-chloropyridin-2-yl, 6-trifluoromethylpyridin-2-yl, 6-difluoromethylpyridin-2-yl, 4-(CH 2 OH)-6-trifluoromethyl-pyridin-2-yl, 4-(CH 2 OH)-6-chloro-pyridin-2-yl, 6-(1,1-difluoroethyl)-4-fluoropyridin-2-yl, 4-trifluoromethylpyrimidin-2-yl, 4-aminopyrimidin-2-yl, 6-trifluoromethyl-4-aminopyrimidin-2-yl, 4-trifluoromethyl-6-aminopyrimidin-2-yl, 4-aminopyrimidin-2-yl, 2-aminopyrimidin-4-yl, 2-aminopyrimidin-5-yl, 4,6-dichloropyridin-2-yl, 3,5-dichlorophenyl, 2,6-difluorophenyl, 2-methyloxazol-4-yl, 4-trifluoromethyl-thiazol-2-yl, 4-methylthiazol-2-yl and phenyl.

3. The compound of claim 1 , wherein ring B′ is selected from 2-(morpholin-4-yl)pyridin-4-yl, 3,5-difluorophenyl, 3-chlorophenyl, 3-cyanomethylphenyl, 3-cyanophenyl, 3-(cyclopropylmethyl)phenyl, 3-cyclopropylaminosulfonylphenyl, 3-dimethylaminosulfonylphenyl, 3-ethyl sulfonylphenyl, 3-fluorophenyl, 3-methyl sulfonylphenyl, 4-fluorophenyl, 3-(1-hydroxyisopropyl)phenyl, 3-methylsulfonyl-5-chlorophenyl, 3-methylsulfonyl-5-fluorophenyl, 3-(N-2,2,2,-trifluoroethylaminosulfonyl)phenyl, 5-chloropyridin-3-yl, 5-cyanopyridin-3-yl, 5-cyanopyridin-3-yl, 5-cyanopyridin-4-yl, 5-fluoropyridin-3-yl, 5-trifluoromethypyridin-3-yl, 2-trifluoromethylpyridin-4-yl, 2-difluoromethylpyridin-4-yl, 2-chloropyridin-4-yl, 6-chloropyridin-4-yl, 6-cyanopyridin-4-yl, 2-cyanopyridin-4-yl, 6-cyclopropylpyridin-4-yl, 6-ethoxypyridin-4-yl, 6-fluoropyridin-3-yl, 2-fluoropyridin-4-yl, 5,6-difluoropyridin-3-yl, 6-fluoropyridin-4-yl, 6-methylpyridin-4-yl, 2-difluoromethylpyridin-4-yl, 6-trifluoromethylpyridin-4-yl, 2-(1-methoxycyclopropyl)pyridin-4-yl, 2-cyclopropylpyridin-4-yl, 2-(propan-1-one)pyridin-4-yl, 2-(1-methylcyclopropyl)pyridin-4-yl, 2-(1-cyanocyclopropyl)pyridin-4-yl, 2-(1-cyanoisopropyl)pyridin-4-yl, isoxazol-4-yl, phenyl, pyridin-4-yl, picolinat-2-yl, pyrimidin-5-yl, 1-propylpyrazol-4-yl, 6-methyl-pyridazin-4-yl, and thiazol-5-yl.

4. The compound of claim 1 , wherein the compound is

or a pharmaceutically acceptable salt thereof.

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

6. A pharmaceutical composition comprising the compound of claim 4 , and a pharmaceutically acceptable carrier.

7. A method of treating a glioblastoma characterized by the presence of an IDH2 mutation, wherein the IDH2 mutation results in a new ability of the enzyme to catalyze the NADPH-dependent reduction of α-ketoglutarate to R(−)-2-hydroxyglutarate in a patient, comprising the step of administering to the patient a therapeutically effective amount of the compound of claim 1 .

8. The method of claim 7 , wherein the IDH2 mutation is an IDH2 R140Q or R172K mutation.

9. The method of claim 7 , wherein the IDH2 mutation is an IDH2 R140Q mutation.

10. The method of claim 7 , further comprising administering to the patient in need thereof a second therapeutic agent useful in the treatment of glioblastoma.

11. A method of treating a glioblastoma characterized by the presence of an IDH2 mutation, wherein the IDH2 mutation results in a new ability of the enzyme to catalyze the NADPH-dependent reduction of a-ketoglutarate to R(−)-2-hydroxyglutarate in a patient, comprising the step of administering to the patient a therapeutically effective amount of the compound of claim 2 .

12. The method of claim 11 , wherein the IDH2 mutation is an IDH2 R140Q or R172K mutation.

13. The method of claim 11 , wherein the IDH2 mutation is an IDH2 R140Q mutation.

14. The method of claim 11 , further comprising administering to the patient in need thereof a second therapeutic agent useful in the treatment of glioblastoma.