Imidazole-containing inhibitors of ALK2 kinase
Disclosed are compounds of formula I, II, III, and IV, and pharmaceutically acceptable salts thereof. The compounds are inhibitors of ALK2 kinase. Also provided are pharmaceutical compositions comprising a compound of formula I, II, III, or IV, or pharmaceutically acceptable salt thereof, and methods involving use of the compounds or pharmaceutically acceptable salts thereof and compositions in the treatment and prevention of various diseases and conditions, such as fibrodysplasia ossificans progressiva.
1. A compound represented by formula (I) or formula (II):
or a pharmaceutically acceptable salt thereof;
wherein:
A is a fused aromatic ring, heteroaromatic ring, partially unsaturated cycloalkyl ring, or partially unsaturated heterocycloalkyl ring optionally substituted by one or more occurrences of R 4 ;
W is C or N;
R a represents H or alkyl;
—R 1 -R 1a represents
wherein R 1a represents optionally substituted heteroaryl;
J represents halo, —OR 2 , —NR 2 R 3 , —C(O)O(alkyl), —C(O)OH, or aryl, wherein aryl is optionally substituted by one or more occurrences of R 2a ;
R 2 represents optionally substituted alkyl, aralkyl, heteroaralkyl, cycloalkyl, heterocycloalkyl, (cycloalkyl)alkyl, (heterocycloalkyl)alkyl, or hydroxyalkyl;
R 3 represents H or alkyl; or
R 2 and R 3 , taken together, form a heterocycloalkyl ring, optionally substituted by one or more occurrences of R 2a ;
R 2a , independently for each occurrence, represents halo, hydroxyl, —C(O)H, oxo, —NH 2 , —C(O)NH 2 , —C(O)OH, —C(O)R 5 , —C(O)OR 5 , —C(O)NH(R 5 ), or optionally substituted alkyl, alkoxyl, hydroxyalkyl, heteroaryl, aryl, aryloxy, heteroaryloxy, arylalkyloxy, heteroarylalkyloxy, or —N(alkyl) 2 ;
or any two geminal or vicinal occurrences of R 2a , taken together, may form a spiro or fused cycloalkyl ring;
R 4 , independently for each occurrence, represents halo, cyano, or optionally substituted alkyl, alkenyl, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxy, aryl, aralkyl, heteroaryl, heteroaralkyl, heterocycloalkyl, heterocycloalkenyl, (heterocycloalkyl)alkyl, cycloalkyl, (cycloalkyl)alkyl, halocycloalkyl, hydroxycycloalkyl, aminocycloalkyl, aryloxy, heteroaryloxy, arylalkyloxy, heteroarylalkyloxy, —CH 2 C(O)NH 2 , —C(O)R 5 , —C(O)OR 5 , or —S(O) 2 R 5 ;
R 5 , independently for each occurrence, represents optionally substituted alkyl, aralkyl, aryl, heteroaralkyl, heteroaryl, cycloalkyl, heterocycloalkyl, (cycloalkyl)alkyl, or (heterocycloalkyl)alkyl; and
R x and R y each independently represent H, alkyl, aralkyl, heteroaralkyl, aryl, heteroaryl, cycloalkyl, heterocycloalkyl, (cycloalkyl)alkyl, (heterocycloalkyl)alkyl, or hydroxyalkyl.
2. The compound of claim 1 , wherein the compound is represented by formula (Ia) or formula (IIa):
wherein:
valence permitting, Q, T, U, and V each independently represent CH, CH 2 , N, NH, O, or SO 2 , wherein any hydrogen of a CH, CH 2 , or NH group is optionally replaced by an occurrence of R 4 ;
R 4 , independently for each occurrence, represents halo, cyano, or optionally substituted alkyl, alkenyl, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxy, aryl, aralkyl, heteroaryl, heteroaralkyl, heterocycloalkyl, heterocycloalkenyl, (heterocycloalkyl)alkyl, cycloalkyl, (cycloalkyl)alkyl, halocycloalkyl, hydroxycycloalkyl, aminocycloalkyl, aryloxy, heteroaryloxy, arylalkyloxy, heteroarylalkyloxy, —CH 2 C(O)NH 2 , —C(O)R 5 , —C(O)OR 5 , or —S(O) 2 R 5 ; and
m is an integer from 0-4, as permitted by valence.
3. The compound of claim 2 , wherein the compound is represented by formula (Ib) or (IIb):
wherein Q represents CH or N; and V represents CH or N.
4. The compound of claim 2 , wherein the compound is represented by formula (Ic) or (IIc):
5. The compound of claim 2 , wherein the compound is represented by formula (Id) or (IId):
wherein T represents CH 2 , NH, 0 , or SO 2 ; and U represents CH 2 , NH, 0 , or SO 2 .
6. The compound of claim 2 , wherein the compound is represented by formula (Ie) or (IIe):
7. The compound of claim 3 , wherein the compound is represented by formula (Ib) or (IIb); and wherein Q is N; and V is CH; or wherein Q is CH; and V is N.
8. The compound of claim 5 , wherein the compound is represented by formula (Id) or (IId); and wherein T is NH; and U is CH 2 ; or wherein T is CH 2 ; and U is NH.
9. The compound of claim 1 , wherein the compound is represented by formula (Ij) or formula (IIj):
wherein:
W is C or N;
valence permitting, X, Y, and Z each independently represent CH, CH 2 , CO, N, NH, O, S, or SO 2 , wherein any hydrogen of a CH, CH 2 , or NH group is optionally replaced by an occurrence of R 4 ;
R 4 , independently for each occurrence, represents cyano, halo, or optionally substituted alkyl, alkenyl, haloalkyl, hydroxyalkyl, aminoalkyl, alkoxy, aryl, aralkyl, heteroaryl, heteroaralkyl, heterocycloalkyl, heterocycloalkenyl, (heterocycloalkyl)alkyl, cycloalkyl, (cycloalkyl)alkyl, halocycloalkyl, hydroxycycloalkyl, aminocycloalkyl, aryloxy, heteroaryloxy, arylalkyloxy, heteroarylalkyloxy, —CH 2 C(O)NH 2 , —C(O)R 5 , —C(O)OR 5 , or —S(O) 2 R 5 ; and
n is an integer from 0-4, as permitted by valence.
10. The compound of claim 9 , wherein the compound is represented by formula (Ik) or (IIk):
wherein X, Y, and Z each independently represent CH, N, NH, O, S, or SO 2 .
11. The compound of claim 10 , wherein the compound is represented by formula (Ik′) or (IIk′):
12. The compound of claim 10 , wherein the compound is represented by formula (Ik″) or (IIk″):
wherein at least one of X and Z is selected from the group consisting of O, N, NH, and S.
13. The compound of claim 12 , wherein
(a) one of X and Z is selected from the group consisting of O, NH, and S; and the other of X and Z is CH;
(b) X is selected from the group consisting of O, NH, and S;
(c) Z is selected from the group consisting of O, NH, and S;
(d) each of X and Z are selected from the group consisting of O, N, NH, and S; or
(e) one of X and Z is N and the other of X and Z is NH.
14. The compound of claim 10 , wherein the compound is represented by formula (In) or (IIn):
wherein each of Y and Z are selected from the group consisting of O, N, NH, and S.
15. The compound of claim 14 , wherein Y is N and Z is NH.
16. The compound of claim 9 , wherein the compound is represented by formula (Im) or (IIm):
wherein X, Y, and Z each independently represent CH 2 , CO, NH, O, S, or SO 2 .
17. The compound of claim 16 , wherein
(a) each of X, Y, and Z is CH 2 ; or
(b) one of X, Y, and Z is NH or O.
18. The compound of claim 1 , wherein R 4 , if present, is selected from the group consisting of optionally substituted alkyl, hydroxyalkyl, aminoalkyl, alkoxy, aryl, aralkyl, and (heterocycloalkyl)alkyl.
19. The compound of claim 1 , wherein R a is H.
20. The compound of claim 1 , wherein —R 1 -R 1a represents
21. The compound of claim 1 , wherein R 1a is optionally substituted quinoline.
22. The compound of claim 1 , wherein J is aryl, optionally substituted by one or more occurrences of R 2a .
23. The compound of claim 1 , wherein J is —NR 2 R 3 .
24. The compound of claim 23 , wherein R 2 and R 3 , taken together, form a heterocycloalkyl ring, optionally substituted by one or more occurrences of R 2a .
25. The compound of claim 24 , wherein R 2 and R 3 , taken together, form a pyrrolidine ring, optionally substituted by one or more occurrences of R 2a .
26. The compound of claim 22 , wherein R 2a , independently for each occurrence, represents —C(O)NH 2 , —C(O)R 5 , hydroxyalkyl, heteroaryl, or aryl.
27. The compound of claim 22 , wherein R 2a is —C(O)NH 2 .
28. The compound of claim 22 , wherein R 2a is hydroxyalkyl.
29. The compound of claim 1 , selected from the following table:
30. A pharmaceutical composition, comprising a compound of claim 1 , or a pharmaceutically acceptable salt thereof; and a pharmaceutically acceptable excipient.
31. A method of inhibiting ALK2 kinase, comprising administering to a subject in need thereof an effective amount of a compound of claim 1 , or a pharmaceutically acceptable salt thereof.
32. A method of treating fibrodysplasia ossificans progressiva, comprising administering to a subject in need thereof a therapeutically effective amount of a compound of claim 1 , or a pharmaceutically acceptable salt thereof.
33. A method of treating a glioma, comprising administering to a subject in need thereof a therapeutically effective amount of a compound of claim 1 , or a pharmaceutically acceptable salt thereof.
34. The method of claim 33 , wherein the glioma is diffuse intrinsic pontine glioma.
35. The compound of claim 24 , wherein R 2a , independently for each occurrence, represents —C(O)NH 2 , —C(O)R 5 , hydroxyalkyl, heteroaryl, or aryl.
36. The compound of claim 25 , wherein R 2a , independently for each occurrence, represents —C(O)NH 2 , —C(O)R 5 , hydroxyalkyl, heteroaryl, or aryl.
37. The compound of claim 1 , wherein the optional substituents are selected from halogen, haloalkyl, hydroxyl, carbonyl, carboxyl, alkoxycarbonyl, formyl, acyl, thiocarbonyl, thioester, thioacetate, thioformate, alkoxyl, alkenyloxy, alkynyloxy, phosphoryl, phosphate, phosphonate, phosphinate, amino, alkylamino, dialkylamino, amido, amidine, imine, cyano, nitro, azido, sulfhydryl, alkylthio, sulfate, sulfonate, sulfamoyl, sulfonamido, sulfonyl, silyl, silyloxy, heterocycloalkyl, cycloalkyl, alkyl, alkenyl, alkynyl, aryl, heteroaryl, arylalkyl, and heteroarylalkyl.