IP Library Granted Patent US 11,248,003
Granted Patent B2
US 11,248,003 · App. 16/766,350 · Granted Feb 15, 2022

Pyrimidine derivative having effect of inhibiting cancer cell growth and pharmaceutical composition containing same

Inventors: Sung-Eun Kim (Seoul, KR); Sunho Lee (Seoul, KR); Rengasamy Rajesh (Suwon-si, KR); Dae Ho Kang (Goyang-si, KR); Hyung Chui Ryu (Hwaseong-si, KR); Jae-Sun Kim (Suwon-si, KR); Sangryul Lee (Chungju-si, KR); Kyong Cheol Kim (Chungju-si, KR); Jin Kyung Rho (Seoul, KR); Jae Cheol Lee (Seoul, KR)
Assignee: ONCOBIX CO., LTD.
C07D495/04A61P35/00C07D401/12C07D473/16C07D487/04
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Quick Facts
Patent No.
US 11,248,003
App. No.
16/766,350
Granted
Feb 15, 2022
Kind
B2
Abstract

A novel pyrimidine derivative compound and a salt thereof are disclosed. The pyrimidine derivative compound effectively inhibits the growth of C797S mutant EGFR-expressed and MET-amplified cancer cells, which are the main resistance mechanisms of third generation EGFR anticancer agents, and thus may be effectively used in the treatment of lung cancer.

Claims (58)

1. A compound of following Chemical Formula 1 or a pharmaceutically acceptable salt thereof:

wherein,

X and Y are each independently carbon or nitrogen,

Z is oxygen or a C1 to C4 alkyl group,

R 1 is a C1 to C4 alkyl group, a C3 to C6 cycloalkyl group, CF 3 , or a dimethylamine group,

R 2 is a C1 to C4 alkyl group,

R 3 is hydrogen or a halogen group,

R 4 is hydrogen, a halogen group, CN, CF 3 , a C1 to C4 alkyl group, or an amino carbonyl group,

R 5 is hydrogen or a C1 to C4 alkyl group,

R 6 is a C1 to C4 alkyl group,

R 7 is hydrogen, an amine group substituted with one or more C1 to C4 alkyl groups, or a piperazinyl group unsubstituted or substituted with one or more C1 to C4 alkyl groups,

when Z is oxygen, Z forms a double bond with S, which forms a single bond with N, or when Z is a C1 to C4 alkyl group, Z forms a single bond with S, which forms a double bond with N, and

R 4 and R 5 may also be connected to form pyrrole, imidazole, or thiophene.

2. The compound or a pharmaceutically acceptable salt thereof according to claim 1 , wherein the compound of Chemical Formula 1 is selected from the following compounds:

N-(2-((5-chloro-2-((2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)-N-methylmethanesulfonamide;

N-(2-((5-chloro-2-((2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)pyrimidin-4-yl)amino)-4-fluorophenyl)-N-methylmethanesulfonamide;

N-(2-((5-chloro-2-((4-(4-(dimethylamino)piperidin-1-yl)-2-methoxyphenyl)amino)pyrimidin-4-yl)amino)phenyl)-N-methylmethanesulfonamide;

N-(2-((5-chloro-2-((2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)-N,P,P-trimethylphosphonic amide;

N-(2-((2-((2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)-7H-purin-6-yl)amino)phenyl)-N-methylmethanesulfonamide;

N-(2-((2-((2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)-5-methylpyrimidin-4-yl)amino)phenyl)-N-methylmethanesulfonamide;

N-(2-((5-cyano-2-((2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)-N-methylmethanesulfonamide;

N-(2-((2-((2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)-5-(trifluoromethyl)pyrimidin-4-yl)amino)phenyl)-N-methylmethanesulfonamide;

2-((2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)-4-((2-(N-methylmethylsulfonamido)phenyl)amino)pyrimidin-5-carboxylamide;

N-(2-((5-chloro-2-((2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)-N-methylethanesulfonamide;

N-(2-((5-chloro-2-((2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)-N-methylpropan-2-sulfonamide;

N-(2-((5-chloro-2-((2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)-N-methylcyclopropansulfonamide;

N-(2-((5-chloro-2-((2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)-1,1,1-trifluoro-N-methylmethanesulfonamide;

N-(2-((5-chloro-2-((2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)-N-methyl(-N′,N′-dimethyl)sulfonamide;

((2-((5-chloro-2-((2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)imino)dimethyl-λ 6 -sulfanone;

N-(2-((5-cyano-2-((2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)pyrimidin-4-yl)amino)-4-fluorophenyl)-N-methylmethanesulfonamide;

N-(2-((5-chloro-2-((2-methoxy-4-(piperidin-4-yl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)-N-methylmethanesulfonamide; and

N-(2-((2-((2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)phenyl)-N-methylmethanesulfonamide.

3. The compound or a pharmaceutically acceptable salt thereof according to claim 1 , wherein

X is nitrogen,

Y is carbon,

Z is oxygen,

R 1 is a C1 to C4 alkyl group,

R 2 is a C1 to C4 alkyl group,

R 3 is hydrogen or a halogen group,

R 4 is a halogen group,

R 5 is hydrogen,

R 6 is a C1 to C4 alkyl group,

R 7 is an amine group substituted with one or more C1 to C4 alkyl groups, or a piperazinyl group unsubstituted or substituted with one or more C1 to C4 alkyl groups.

4. The compound or a pharmaceutically acceptable salt thereof according to claim 3 , wherein the compound of Chemical Formula 1 is selected from the following compounds:

N-(2-((5-chloro-2-((2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)-N-methylmethanesulfonamide;

N-(2-((5-chloro-2-((2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)pyrimidin-4-yl)amino)-4-fluorophenyl)-N-methylmethanesulfonamide; and

N-(2-((5-chloro-2-((4-(4-(dimethylamino)piperidin-1-yl)-2-methoxyphenyl)amino)pyrimidin-4-yl)amino)phenyl)-N-methylmethanesulfonamide.

5. The compound or a pharmaceutically acceptable salt thereof according to claim 1 , wherein the pharmaceutically acceptable salt is a salt of an acid selected from the group consisting of hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, nitric acid, acetic acid, glycolic acid, lactic acid, pyruvic acid, malonic acid, succinic acid, glutaric acid, fumaric acid, malic acid, mandelic acid, tartaric acid, citric acid, ascorbic acid, palmitic acid, maleic acid, benzoic acid, hydroxybenzoic acid, phenylacetic acid, cinnamic acid, salicylic acid, methanesulfonic acid, ethanesulfonic acid, benzenesulfonic acid, and toluenesulfonic acid.

6. A pharmaceutical composition comprising the compound or the pharmaceutically acceptable salt thereof according to claim 1 as an active ingredient, and a pharmaceutically acceptable carrier.

7. A pharmaceutical composition comprising the compound or the pharmaceutically acceptable salt thereof according to claim 2 as an active ingredient, and a pharmaceutically acceptable carrier.

8. A pharmaceutical composition comprising the compound or the pharmaceutically acceptable salt thereof according to claim 3 as an active ingredient, and a pharmaceutically acceptable carrier.

9. A pharmaceutical composition comprising the compound or the pharmaceutically acceptable salt thereof according to claim 4 as an active ingredient, and a pharmaceutically acceptable carrier.

10. A pharmaceutical composition comprising the compound or the pharmaceutically acceptable salt thereof according to claim 5 as an active ingredient, and a pharmaceutically acceptable carrier.

11. A method for treating lung cancer in a subject in need thereof comprising administering the composition of claim 6 to the subject.

12. A method for treating lung cancer in a subject in need thereof comprising administering the composition of claim 7 to the subject.

13. A method for treating lung cancer in a subject in need thereof comprising administering the composition of claim 8 to the subject.

14. A method for treating lung cancer in a subject in need thereof comprising administering the composition of claim 9 to the subject.

15. A method for treating lung cancer in a subject in need thereof comprising administering the composition of claim 10 to the subject.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 22, 2020
From: KIM, SUNG-EUN; LEE, SUNHO; RAJESH, RENGASAMY; KANG, DAE HO; RYU, HYUNG CHUL; KIM, JAE-SUN; LEE, SANGRYUL; KIM, KYONG CHEOL; RHO, JIN KYUNG; LEE, JAE CHEOL
To: ONCOBIX CO., LTD.
Reel/Frame 052742/0588 →
Priority Claims (2)
KR 10-2017-0167809 · Dec 7, 2017 · national
KR 10-2018-0154838 · Dec 5, 2018 · national
Continuity (1)
Related Publication 20210147439A1 · May 20, 2021