Antimalarial agents

Inventors: John A. McCauley (Maple Glen, PA); Manuel de Lera Ruiz (Perkasie, PA); Zhuyan Guo (Scotch Plains, NJ); Bin Hu (Shanghai, CN); Michael J. Kelly, III (Paoli, PA); Zhiyu Lei (Shanghai, CN); David B. Olsen (Lansdale, PA); Brad Sleebs (Bundoora, AU); Dongmei Zhan (Shanghai, CN); Lianyun Zhao (Shanghai, CN)

Assignees: Merch Sharpe & Dohme LLC; MSD R&D (China) Co. LTD; The Walter and Eliza Hall Institute of Medical Research

C07D239/22 A61P33/06 C07D401/06 C07D405/14

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Quick Facts

Patent No.: US 12,338,219
App. No.: 17/776,040
Granted: Jun 24, 2025
Kind: B2

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Abstract

The present invention provides methods of treating malaria comprising administration of compounds of Formula (I) or a pharmaceutically acceptable salt thereof, to a subject in need thereof, wherein the variables are as defined herein. The invention also provides uses of the compounds of Formula (I), as defined herein, for the possible inhibition of plasmepsin X, plasmepsin IX or plasmepsin X and IX activity, for treating a Plasmodium infection, and for treating malaria. Also provided are methods of treatment further comprising administration of one or more additional anti-malarial compounds.

Claims (31)

1. A compound having the structural Formula (I):

or a pharmaceutically acceptable salt thereof, wherein:

R 1 is a heterocycloalkyl, C 3 -C 12 cycloalkyl, aryl or C 1 -C 6 alkylaryl, wherein the heterocycloalkyl, C 3 -C 12 cycloalkyl, aryl, C 1 -C 6 alkylaryl is unsubstituted or substituted with 1 to 5 substituents independently selected from the group consisting of halogen, CN, OH, alkoxy, haloalkoxy, C 1 -C 6 alkylOC 1 -C 6 alkyl, C 1 -C 6 alkylCOOH, COOH, oxo, COOC 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, spiroC 3 -C 6 cycloalkyl, C 1 -C 6 alkyl, haloC 1 -C 6 alkyl, C 1 -C 6 alkylOH, CON(R 7 )(R 8 ), N(R 7 )(R 8 ) and C 1 -C 6 alkylN(R 7 )(R 8 );

R 2 is hydrogen, C 1 -C 6 alkylCOOH, COOH, C 3 -C 6 cycloalkyl, C 1 -C 6 alkyl, haloC 1 -C 6 alkyl or C 1 -C 6 alkylOH;

R 3 is hydrogen, halogen, CN, OH, C 3 -C 6 cycloalkyl or C 1 -C 6 alkyl;

R 4 is hydrogen, halogen, CN, OH, C 3 -C 6 cycloalkyl or C 1 -C 6 alkyl;

R 5 is hydrogen, halogen, CN, OH, alkoxy, C 1 -C 6 alkylOC 1 -C 6 alkyl, C 1 -C 6 alkylCOOH, COOH, C 3 -C 6 cycloalkyl, C 1 -C 6 alkyl, haloC 1 -C 6 alkyl, C 1 -C 6 alkylOH, CON(R 7 )(R 8 ), N(R 7 )(R 8 ) or C 1 -C 6 alkylN(R 7 )(R 8 ) or when taken with R 6 forms a C 3 -C 6 cycloalkyl or C 3 -C 6 heterocycloalkyl;

R 6 is hydrogen, halogen, CN, OH, alkoxy, C 1 -C 6 alkylOC 1 -C 6 alkyl, C 1 -C 6 alkylCOOH, COOH, C 3 -C 6 cycloalkyl, C 1 -C 6 alkyl, haloC 1 -C 6 alkyl, C 1 -C 6 alkylOH, CON(R 7 )(R 8 ), N(R 7 )(R 8 ) or C 1 -C 6 alkylN(R 7 )(R 8 ) or when taken with R 5 forms a C 3 -C 6 cycloalkyl or C 3 -C 6 heterocycloalkyl;

R 7 is hydrogen, C 1 -C 6 alkylCOOH, COOH, C 3 -C 6 cycloalkyl, C 1 -C 6 alkyl, haloC 1 -C 6 alkyl or C 1 -C 6 alkylOH;

R 8 is hydrogen, C 1 -C 6 alkylCOOH, COOH, C 3 -C 6 cycloalkyl, C 1 -C 6 alkyl, haloC 1 -C 6 alkyl or C 1 -C 6 alkylOH; and

R 9 is hydrogen, halogen, CN, alkoxy, C 1 -C 6 alkyl, heterocycloalkyl, heteroaryl, C 3 -C 12 cycloalkyl, aryl, COOH, oxo, COOC 1 -C 6 alkyl, haloC 1 -C 6 alkyl, OH, CON(R 7 )(R 8 ) and N(R 7 )(R 8 ), wherein the C 1 -C 6 alkyl can be unsubstituted or substituted with one, two or three substituents selected from the group consisting of halogen, CN, OH, alkoxy, heterocycloalkyl, heteroaryl, C 3 -C 12 cycloalkyl, aryl, COOH, oxo, COOC 1 -C 6 alkyl, haloC 1 -C 6 alkyl, OH, CON(R 7 )(R 8 ) and N(R 7 )(R 8 ), and wherein the heterocycloalkyl, heteroaryl, C 3 -C 12 cycloalkyl and aryl can be unsubstituted or substituted with one, two or three substituents selected from the group consisting of halogen, CN, OH, alkoxy, C 1 -C 6 alkyl, COOH, oxo, COOC 1 -C 6 alkyl, haloC 1 -C 6 alkyl, OH, CON(R 7 )(R 8 ) and N(R 7 )(R 8 ).

2. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 1 is selected from the group consisting of:

wherein R 1 is unsubstituted or substituted with 1 to 5 substituents selected from the group consisting of halogen, CN, OH, alkoxy, haloalkoxy, C 1 -C 6 alkylOC 1 -C 6 alkyl, C 1 -C 6 alkylCOOH, COOH, oxo, COOC 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, spiroC 3 -C 6 cycloalkyl, C 1 -C 6 alkyl, haloC 1 -C 6 alkyl, C 1 -C 6 alkylOH, CON(R 7 )(R 8 ), N(R 7 )(R 8 ) and C 1 -C 6 alkylN(R 7 )(R 8 );

R 7 is hydrogen, C 1 -C 6 alkylCOOH, COOH, C 3 -C 6 cycloalkyl, C 1 -C 6 alkyl, haloC 1 -C 6 alkyl or C 1 -C 6 alkylOH; and

R 8 is hydrogen, C 1 -C 6 alkylCOOH, COOH, C 3 -C 6 cycloalkyl, C 1 -C 6 alkyl, haloC 1 -C 6 alkyl or C 1 -C 6 alkylOH.

3. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 1 is:

wherein R 1 is unsubstituted or substituted with 1 to 5 substituents selected from the group consisting of halogen, CN, OH, alkoxy, haloalkoxy, C 1 -C 6 alkylOC 1 -C 6 alkyl, oxo, COOC 1 -C 6 alkyl, C 1 -C 6 alkyl, haloC 1 -C 6 alkyl and C 1 -C 6 alkylOH.

4. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 1 is:

5. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 2 is hydrogen.

6. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 1 is a chromane or indane moiety.

7. The compound of claim 6 , or a pharmaceutically acceptable salt thereof, wherein R 1 is:

8. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 3 is selected from hydrogen, halogen or C 1 -C 6 alkyl.

9. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 4 is selected from hydrogen, halogen or C 1 -C 6 alkyl.

10. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 5 and R 6 are independently selected from hydrogen or C 1 -C 6 alkyl.

11. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 5 and R 6 are independently selected from methyl or ethyl.

12. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 9 is hydrogen, C 1 -C 6 alkyl, heteroaryl, or aryl, wherein the C 1 -C 6 alkyl, heteroaryl or aryl can be unsubstituted or substituted with one, two or three substituents selected from the group consisting of halogen, CN, OH, alkoxy.

13. A compound selected from the group consisting of:

14. A pharmaceutical composition comprising a compound of claim 1 or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

15. A method for treating a Plasmodium infection, or for treating malaria, which comprises administering to a subject in need of such treatment a therapeutically effective amount of a compound of claim 1 , or a pharmaceutically acceptable salt thereof.

16. A method for treating a Plasmodium infection, or for treating malaria, comprising administration of a compound of claim 1 , or a pharmaceutically acceptable salt thereof, and an effective amount of one or more additional anti-malarial agents.

Assignments (6)