Compounds, compositions and methods
Certain substituted urea derivatives selectively modulate the cardiac sarcomere, for example by potentiating cardiac myosin, and are useful in the treatment of systolic heart failure including congestive heart failure.
1. A compound of Formula 3B:
or a pharmaceutically acceptable salt thereof.
2. A compound of Formula 3C:
or a pharmaceutically acceptable salt thereof, wherein R is selected from the group consisting of O and NH.
3. A compound of Formula 3D:
or a pharmaceutically acceptable salt thereof.
4. A method of preparing a compound of Formula 3D:
or a pharmaceutically acceptable salt thereof, comprising
contacting a compound of Formula 3C:
wherein R is selected from the group consisting of O and NH, with methyl piperazine-1-carboxylate and a reducing agent to yield the compound of Formula 3D.
5. The method of claim 4 , wherein the compound of Formula 3C is prepared by reducing a compound of Formula 3B:
in the presence of a reducing agent to yield the compound of Formula 3C.
6. The method of claim 5 , wherein the compound of Formula 3B is prepared by contacting a compound of Formula 3A:
with sodium cyanide and nickel (II) bromide in an organic solvent to yield the compound of Formula 3B.
7. The method of claim 6 , wherein the sodium cyanide is present in an amount of at least 2 equivalents relative to the amount of the compound of Formula 3A.
8. The method of claim 6 , wherein the nickel (II) bromide is present in an amount of at least 1 equivalent relative to the amount of the compound of Formula 3A.
9. The method of claim 6 , wherein the organic solvent is 1-methyl-2-pyrrolidinone (NMP).
10. The method of claim 6 , wherein the reaction mixture is heated to between 195° C. and 205° C.
11. The method of claim 5 , wherein the reducing agent is present in an amount of at least 2 equivalents relative to the amount of the compound of Formula 3B.
12. The method of claim 5 , wherein the internal reaction temperature is maintained at ≤0° C. during the addition of the reducing agent.
13. The method of claim 5 , wherein the reducing agent used to form the compound of Formula 3C comprises diisobutyllithiumaluminum hydride (DIBAlH).
14. The method of claim 5 , wherein the DIBAlH is present in an amount of at least 2 equivalents relative to the amount of the compound of Formula 3B.
15. The method of claim 5 , wherein the compound of Formula 3C comprises a mixture of compounds 3C-A and 3C-B:
16. The method of claim 4 , wherein the methyl piperazine-1-carboxylate is present in an amount of at least 1 equivalent relative to the amount of the compound of Formula 3C.
17. The method of claim 4 , wherein the reducing agent used to form the compound of Formula 3D comprises sodium triacetoxyborohydride.
18. The method of claim 4 , wherein the internal reaction temperature is maintained below about 45° C. during the addition of the reducing agent.
19. The method of claim 4 , wherein the sodium triacetoxyborohydride is present in an amount of at least 1.5 equivalents relative to the amount of the compound of Formula 3C.