Pseudopolymorphic Forms Of A HIV Protease Inhibitor
New pseudopolymorphic forms of (3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl(1S,2R)-3-[[(4-aminophenyl)sulfonyl](isobutyl)amino]-1-benzyl-2-hydroxypropylcarbamate and processes for producing them are disclosed.
1 - 15 . (canceled)
16 . An alcohol solvate of the compound (3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl(1S,2R)-3-[[(4-aminophenyl)sulfonyl](isobutyl)amino]-1-benzyl-2-hydroxypropylcarbamate.
17 . The alcohol solvate of claim 16 , wherein the alcohol is a C1-C4 alcohol.
18 . The alcohol solvate of claim 16 , wherein the alcohol is a C1 alcohol, a C3 alcohol, or a C4 alcohol.
19 . The alcohol solvate of claim 16 , wherein the alcohol is a C1 alcohol.
20 . The alcohol solvate of claim 16 , wherein the alcohol is a C3 alcohol.
21 . The alcohol solvate of claim 16 , wherein the alcohol is a C4 alcohol.
22 . A composition comprising an alcohol solvate of the compound (3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl(1S,2R)-3-[[(4-aminophenyl)sulfonyl](isobutyl)amino]-1-benzyl-2-hydroxypropylcarbamate and a carrier.
23 . The composition of claim 22 , wherein the alcohol is a C1 alcohol, a C3 alcohol, or a C4 alcohol.
24 . The composition of claim 22 , wherein the alcohol is a C1 alcohol.
25 . The composition of claim 22 , wherein the alcohol is a C3 alcohol.
26 . The composition of claim 22 , wherein the alcohol is a C4 alcohol.
27 . A method of treating a mammal having an HIV infection comprising administering to the mammal, a therapeutically effective amount of an alcohol solvate of the compound (3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl(1S,2R)-3-[[(4-aminophenyl)sulfonyl](isobutyl)amino]-1-benzyl-2-hydroxypropylcarbamate.
28 . The method of claim 27 , wherein the alcohol solvate is administered in an amount sufficient to reduce the viral load of the HIV, increase CD4+ cell count, or inhibit HIV protease activity.
29 . The method of claim 27 , wherein the alcohol is a C1-C4 alcohol.
30 . The method of claim 27 , wherein the alcohol is a C1 alcohol.
31 . The method of claim 27 , wherein the alcohol is a C2 alcohol.
32 . The method of claim 27 , wherein the alcohol is a C3 alcohol.
33 . The method of claim 27 , wherein the alcohol is a C4 alcohol.