Azepane derivatives and methods of treating hepatitis B infections
Provided herein are compounds useful for the treatment of HBV infection in a subject in need thereof, pharmaceutical compositions thereof, and methods of inhibiting, suppressing, or preventing HBV infection in the subject. In an embodiment of the compounds provided herein, the compounds are of Formula Va:
1. A compound of Formula Va:
or a pharmaceutically acceptable salt thereof;
wherein
each R 1 is, independently at each occurrence, halo, OH, —C 1 -C 6 alkyl, or —O—C 1 -C 6 alkyl, wherein the alkyl groups are optionally substituted 1-3 times with halo or OH;
each R 2 is, independently at each occurrence, halo, OH, —C 1 -C 6 alkyl, or —O—C 1 -C 6 alkyl, wherein the alkyl groups are optionally substituted 1-3 times with halo or OH;
x is 2 or 3;
Cy is
and R 11 is, independently at each occurrence, —OH, halo, —C 1 -C 6 alkyl, —OC(O)CH 3 , or —H 2 PO 4 , wherein n and m are 1, 2, or 3, and at least one R 11 is
2. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein each R 1 is, independently at each occurrence, halo.
3. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein each R 2 is, independently at each occurrence, halo or —C 1 -C 6 alkyl, wherein the alkyl is optionally substituted 1-3 times with halo.
4. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the compound is selected from:
5. A pharmaceutical composition comprising a compound of claim 1 , or a pharmaceutically acceptable salt thereof, together with a pharmaceutically acceptable carrier.
6. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the compound is