Derivatives of succinic and glutaric acids and analogs thereof useful as inhibitors of phex
The present invention relates to derivatives of succinic and glutaric acids and analogues thereof, having the following general formula: useful as inhibitors of PHEX. These derivatives are useful for promoting generation of bone mass and treating or preventing diseases or conditions associated with a phosphate metabolism defect. Methods for preparation and intermediates are also disclosed.
1. A compound of Formula (I), or a pharmaceutically acceptable salt thereof:
wherein
A is a zinc ligand or zinc ligand bearing moiety selected from the group consisting of:
B is absent:
R is hydrogen or lower alkyl;
R 1 is hydrogen or lower alkyl;
R 2 is hydrogen, or lower alkyl;
R 3 is hydrogen or lower alkyl;
R 4 is lower alkyl, substituted lower alkyl, cycloalkyl-(CH 2 ) w —, aryl-(CH 2 ) w —, substituted aryl —(CH 2 ) w — or heteroaryl-(CH 2 ) w —;
R 5 is hydrogen, lower alkyl, substituted lower alkyl, cycloalkyl-(CH 2 ) x —, aryl-(CH 2 ) x —, substituted aryl-(CH 2 ) x —, or heteroaryl-(CH 2 ) x —;
R 8 and R 9 are independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, aryl-(CH 2 ) y —, substituted aryl-(CH 2 ) y —, heteroaryl-(CH 2 ) y —,
R 10 is alkyl, substituted alkyl, cycloalkyl-(CH 2 ) y , aryl-(CH 2 ) y —, substituted aryl-(CH 2 ) y — or heteroaryl-(CH 2 ) y —;
R 13 is hydrogen, lower alkyl, cycloalkyl or phenyl;
R 14 is hydrogen, lower alkyl, lower alkoxy or phenyl;
R 15 is lower alkyl or aryl-(CH 2 ) y —;
D is —COOH,
E is hydrogen, —COOH, —CONH 2 , —CONH(lower alkyl), —CON(lower alkyl) 2 , —CONH—(CH 2 ) z -aryl, —CON(—(CH 2 ) z -aryl) 2 , —CO-amino acid, —CH 2 COOH, CH 2 OH, —CH 2 CH 2 OH, or —COOR 16 ;
R 16 is selected from the group consisting of hydrogen, alkyl, substituted alkyl, aryl-(CH 2 ) y —, substituted aryl-(CH 2 ) y —, heteroaryl-(CH 2 ) y —,
C is carbon;
H is hydrogen;
O is oxygen;
N is nitrogen;
S is sulfur;
P is phosphorus;
v is zero;
w is zero or an integer ranging from 1 to 4;
x is an integer ranging from 1 to 4;
y is zero or an integer ranging from 1 to 6; and
z is zero, one, two, or three.
2. The compound of claim 1 , wherein R 1 and R 3 , when v=0, are connected together to form an alkylene bridge of 3 carbon atoms representing with the carbon atoms to which they are attached a cyclopentane ring.
3. The compound of claim 1 , wherein R 1 and R 3 , when v=0, are connected together to form an alkylene bridge of 4 carbon atoms representing with the carbon atoms to which they are attached a cyclohexane ring.
4. The compound of claim 1 , wherein R and R 4 are connected together to form an alkylene bridge of 3 carbon atoms representing with the nitrogen and carbon atoms to which they are attached a pyrrolidine ring.
5. The compound of claim 1 , wherein R and R 4 are connected together to form an alkylene bridge of 4 carbon atoms representing with the nitrogen and carbon atoms to which they are attached a piperidine ring.
6. The compound of claim 1 , wherein the compound is further defined as: 3-(2-Biphenyl-4-yl-ethylcarbamoyl)-4-hydroxycarbamoyl-butyric acid; 3-[2-(4′-Cyano-biphenyl-4-yl)-ethylcarbamoyl]-4-hydroxycarbamoyl-butyric acid; 4-Hydroxycarbamoyl-3-[2-(4-pyridin-2-yl-phenyl)-ethylcarbamoyl]-butyric acid; 4-Hydroxycarbamoyl-3-(4-phenyl-butylcarbamoyl)-butyric acid; 4-Hydroxycarbamoyl-3-(2-phenoxy-ethylcarbamoyl)-butyric acid; 3-[2-(4′-Hydroxy-biphenyl-4-yl)-ethylcarbamoyl]-4-hydroxycarbamoyl-butyric acid; 3-(2,2-Diphenyl-ethylcarbamoyl)-4-hydroxycarbamoyl-butyric acid; 3-[2-(4′-Dimethylamino-biphenyl-4-yl)-ethylcarbamoyl]-4-hydroxycarbamoyl-butyric acid; 4-Hydroxycarbamoyl-3-(5-hydroxy-pentylcarbamoyl)-butyric acid; 3-[(Biphenyl-4-ylmethyl)-carbamoyl]-4-hydroxycarbamoyl-butyric acid; N-[1-carboxy-2-(1H-indol-3-yl)-ethyl]-3-(3-phenyl-1-phosphono-propylamino)-succinic acid; or 3-(2-Naphthalen-2-yl-ethylcarbamoyl)-pentanedioic acid.
7. The compound of claim 6 , wherein the compound is 3-(2-Biphenyl-4-yl-ethylcarbamoyl)-4-hydroxycarbamoyl-butyric acid.
8. A pharmaceutical composition comprising a therapeutically effective amount of a compound of claim 1 and a physiologically acceptable carrier or excipient.
9. The pharmaceutical composition of claim 8 , wherein the compound is further defined as: 3-(2-Biphenyl-4-yl-ethylcarbamoyl)-4-hydroxycarbamoyl-butyric acid; 3-[2-(4′-Cyano-biphenyl-4-yl)-ethylcarbamoyl]-4-hydroxycarbamoyl-butyric acid; 4-Hydroxycarbamoyl-3-[2-(4-pyridin-2-yl-phenyl)-ethylcarbamoyl]-butyric acid; 4-Hydroxycarbamoyl-3-(4-phenyl-butylcarbamoyl)-butyric acid; 4-Hydroxycarbamoyl-3-(2-phenoxy-ethylcarbamoyl)-butyric acid; 3-[2-(4′-Hydroxy-biphenyl-4-yl)-ethylcarbamoyl]-4-hydroxycarbamoyl-butyric acid; 3-(2,2-Diphenyl-ethylcarbamoyl)-4-hydroxycarbamoyl-butyric acid; 3-[2-(4′-Dimethylamino-biphenyl-4-yl)-ethylcarbamoyl]-4-hydroxycarbamoyl-butyric acid; 4-Hydroxycarbamoyl-3-(5-hydroxy-pentylcarbamoyl)-butyric acid; 3-[(Biphenyl-4-ylmethyl)-carbamoyl]-4-hydroxycarbamoyl-butyric acid; N-[1-carboxy-2-(1H-indol-3-yl)-ethyl]-3-(3-phenyl-1-phosphono-propylamino)-succinic acid; or 3-(2-Naphthalen-2-yl-ethylcarbamoyl)-pentanedioic acid.
10. The pharmaceutical composition of claim 8 , wherein the compound is 3-(2-Biphenyl-4-yl-ethylcarbamoyl)-4-hydroxycarbamoyl-butvric acid.
11. The compound of claim 1 , wherein A is
12. The compound of claim 1 , wherein A is
13. The compound of claim 1 , wherein A is
14. The compound of claim 1 , wherein A is
15. The compound of claim 1 having the formula:
16. The pharmaceutical composition of claim 9 , wherein the compound is further defined as 3-[2-(4′-Cyano-biphenyl-4-yl)-ethylcarbamoyl]-4-hydroxycarbamoyl-butyric acid.
17. The pharmaceutical composition of claim 9 , wherein the compound is further defined as 4-Hydroxycarbamoyl-3-[2-(4-pyridin-2-yl-phenyl)-ethylcarbamoyl]-butyric acid.
18. The pharmaceutical composition of claim 9 , wherein the compound is further defined as 4-Hydroxycarbamoyl-3-(4-phenyl-butylcarbamoyl)-butyric acid.
19. The pharmaceutical composition of claim 9 , wherein the compound is further defined as 4-Hydroxycarbamoyl-3-(2-phenoxy-ethylcarbamoyl)-butyric acid.
20. The pharmaceutical composition of claim 9 , wherein the compound is further defined as 3-[2-(4′-Hydroxy-biphenyl-4-yl)-ethylcarbamoyl]-4-hydroxycarbamoyl-butyric acid.
21. The pharmaceutical composition of claim 9 , wherein the compound is further defined as 3-(2,2-Diphenyl-ethylcarbamoyl)-4-hydroxycarbamoyl-butyric acid.
22. The pharmaceutical composition of claim 9 , wherein the compound is further defined as 3-[2-(4′-Dimethylamino-biphenyl-4-yl)-ethylcarbamoyl]-4-hydroxycarbamoyl-butyric acid.
23. The pharmaceutical composition of claim 9 , wherein the compound is further defined as 4-Hydroxycarbamoyl-3-(5-hydroxy-pentylcarbamoyl)-butyric acid.
24. The pharmaceutical composition of claim 9 , wherein the compound is further defined as 3-[(Biphenyl-4-ylmethyl)-carbamoyl]-4-hydroxycarbamoyl-butyric acid.
25. The pharmaceutical composition of claim 9 , wherein the compound is further defined as N-[1-carboxy-2-(1H-indol-3-yl)-ethyl]-3-(3-phenyl-1-phosphono-propylamino)-succinic acid.
26. The pharmaceutical composition of claim 9 , wherein the compound is further defined as 3-(2-Naphthalen-2-yl-ethylcarbamoyl)-pentanedioic acid.