DEUTERIUM-ENRICHED MARAVIROC
The present application describes deuterium-enriched maraviroc, pharmaceutically acceptable salt forms thereof, and methods of treating using the same.
1 . A deuterium-enriched compound of formula I or a pharmaceutically acceptable salt thereof:
wherein R 1 -R 41 are independently selected from H and D; and
the abundance of deuterium in R 1 -R 41 is at least 2%.
2 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 1 -R 41 is selected from at least 2%, at least 5%, at least 10%, at least 15%, at least 20%, at least 24%, at least 29%, at least 34%, at least 39%, at least 44%, at least 49%, at least 54%, at least 59%, at least 63%, at least 68%, at least 73%, at least 78%, at least 83%, at least 88%, at least 93%, and 100%.
3 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 1 is selected from at least 100%.
4 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 10 and R 32 -R 35 is selected from at least 20%, at least 40%, at least 60%, at least 80%, and 100%.
5 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 1 , R 10 and R 32 -R 35 is selected from at least 17%, at least 33%, at least 50%, at least 67%, at least 83%, and 100%.
6 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 2 -R 10 is selected from at least 11%, at least 22%, at least 33%, at least 44%, at least 56%, at least 67%, at least 78%, 100%.
7 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 11 , R 17 -R 20 is selected from at least 20%, at least 40%, at least 60%, at least 80%, and 100%.
8 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 12 -R 16 is selected from at least 20%, at least 40%, at least 60%, at least 80%, and 100%.
9 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 21 -R 31 is selected from at least 9%, at least 18%, at least 27%, at least 36%, at least 45%, at least 56%, at least 64%, at least 73%, at least 82%, at least 91%, and 100%.
10 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 32 -R 34 is selected from at least 33%, at least 67%, and 100%.
11 . A deuterium-enriched compound of claim 1 , wherein the abundance of deuterium in R 35 -R 41 is selected from at least 14%, at least 29%, at least 43%, at least 57%, at least 71%, at least 86%, and 100%.
12 . A deuterium-enriched compound of claim 1 , wherein the compound is selected from compounds 1-10 of Table 1.
13 . A deuterium-enriched compound of claim 1 , wherein the compound is selected from compounds 11-20 of Table 2.
14 . An isolated deuterium-enriched compound of formula I or a pharmaceutically acceptable salt thereof:
wherein R 1 -R 41 are independently selected from H and D; and
the abundance of deuterium in R 1 -R 41 is at least 2%.
15 . An isolated deuterium-enriched compound of claim 14 , wherein the compound is selected from compounds 1-10 of Table 1.
16 . An isolated deuterium-enriched compound of claim 14 , wherein the compound is selected from compounds 11-20 of Table 2.
17 . A mixture of deuterium-enriched compounds of formula I or a pharmaceutically acceptable salt thereof:
wherein R 1 -R 41 are independently selected from H and D; and
the abundance of deuterium in R 1 -R 41 is at least 2%.
18 . A mixture of deuterium-enriched compound of claim 17 , wherein the compound is selected from compounds 1-10 of Table 1.
19 . A mixture of deuterium-enriched compound of claim 17 , wherein the compound is selected from compounds 11-20 of Table 2.
20 . A pharmaceutical composition, comprising: a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound of claim 1 or a pharmaceutically acceptable salt form thereof.
21 . A method for treating Human immunodeficiency virus comprising: administering, to a patient in need thereof, a therapeutically effective amount of a compound of claim 1 or a pharmaceutically acceptable salt form thereof.