Sulfonamide inhibitors of aspartyl protease

Abstract

The present invention relates to a novel class of sulfonamides which are aspartyl protease inhibitors. In one embodiment, this invention relates to a novel class of HIV aspartyl protease inhibitors characterized by specific structural and physicochemical features. This invention also relates to pharmaceutical compositions comprising these compounds. The compounds and pharmaceutical compositions of this invention are particularly well suited for inhibiting HIV-1 and HIV-2 protease activity and consequently, may be advantageously used as anti-viral agents against the HIV-1 and HIV-2 viruses. This invention also relates to methods for inhibiting the activity of HIV aspartyl protease using the compounds of this invention and methods for screening compounds for anti-HIV activity.

We claim:  
     
         1 . A compound of formula (I):  
       
         
           
           
               
               
           
         
       
       wherein: 
 A is selected from H; Ht; —R 1 -Ht; —R 1 —C 1 -C 6  alkyl, which is optionally substituted with one or more groups independently selected from hydroxy, C 1 -C 4  alkoxy, Ht, —O-Ht, —NR 2 —CO—N(R 2 ) 2  or —CO—N(R 2 ) 2 ; —R 1 —C 2 -C 6  alkenyl, which is optionally substituted with one or more groups independently selected from hydroxy, C 1 -C 4  alkoxy, Ht, —O-Ht, —NR 2 —CO—N(R 2 ) 2  or —CO—N(R 2 ) 2 ; or R 7 ;  
 each R 1  is independently selected from —C(O)—, —S(O) 2 —, —C(O)—C(O)—, —O—C(O)—, —O—S(O) 2 , —NR 2 —S(O) 2 —, —NR 2 —CO)— or —NR 2 —C(O)—C(O)—;  
 each Ht is independently selected from C 3 -C 7  cycloalkyl; C 2 -C 2  cycloalkenyl; C 6 -C 10  aryl; or a 5-7 membered saturated or unsaturated heterocycle, containing one or more heteroatoms selected from N, N(R 2 ), O, S and S(O) n ; wherein said aryl or said heterocycle is optionally fused to Q; and wherein any member of said Ht is optionally substituted with one or more substituents independently selected from oxo, —OR 2 , SR 2 , —R 2 , —N(R 2 )(R 2 ), —R 2 —OH, —CN, —CO 2 R 2 , —C(O)—N(R 2 ) 2 , —S(O) 2 —N(R 2 ) 2 , —N(R 2 )—C(O)—R 2 , —C(O)—R 2 , —S(O) n —R 2 , —OCF 3 , —S(O) n -Q, methylenedioxy, —N(R 2 )—S(O) 2  (R 2 ) halo, —CF 3 , —NO 2 , Q, —OQ, —OR 7 , —SR 7 , —R 7 , —N(R)(R 7 ) or —N(R 7 ) 2 ;  
 each R 2  is independently selected from H, Ht or C 1 -C 6  alkyl optionally substituted with Q or R 10 ;  
 B, when present, is —N(R 2 )—C(R 3 ) 2 —C(O)—;  
 each x is independently 0 or 1;  
 each R 3  is independently selected from H, Ht, C 1 -C 6  alkyl, C 2 -C 6  alkenyl, C 3 -C 6  cycloalkyl or C 5 -C 6  cycloalkenyl; wherein any member of said R 3 , except H, is optionally substituted with one or more substituents selected from —OR 2 , —C(O)—NH—R 2 , —S(O) n —N(R 2 )(R 2 ), Ht, —CN, —SR 2 , CO 2 R 2 , NR 2 —C(O)—R 2 ;  
 each n is independently 1 or 2;  
 G, when present, is selected from H, R 7  or C 1 -C 4  alkyl, or, when G is C 1 -C 4  alkyl, G and R 7  are bound to one another either directly or through a C 1 -C 3  linker to form a heterocyclic ring; or  
 when G Is not present, the nitrogen to which G is attached is bound directly to the R 7  group in —OR 7  with the concomitant displacement of one -ZM group from R 7 ;  
 D is selected from Q; C 1 -C 6  alkyl or C 2 -C 4  alkenyl, which is optionally substituted with one or more groups selected from C 3 -C 6  cycloalkyl, —OR 2 , —S-Ht, —R 3 , —O-Q or Q; C 3 -C 6  cycloalkyl or C 5 -C 6  cycloalkenyl, which is optionally substituted with or fused to Q;  
 each Q is independently selected from a 3-7 membered saturated, partially saturated or unsaturated carbocyclic ring system; or a 5-7 membered saturated, partially saturated or unsaturated heterocyclic ring containing one or more heteroatoms selected from O, N, S, S(O) n  or N(R 2 ); wherein Q is optionally substituted with one or more groups selected from oxo, —OR 2 , —R 2 , —N(R 2 ) 2 , —N(R 2 )C(O)—R 2 , —R 2 —OH, —CN, —CO 2 R 2 , —C(O)—N(R 2 ) 2 , halo or —CF 3 ;  
 D′ is selected from —OR 10 , —N═R 10  or —N(R 10 )—R 1 —R 3 ;  
 E is selected from Ht; O-Ht; Ht-Ht; —O—R 3 ; —N(R 2 )(R 3 ); C 1 -C 6  alkyl, which is optionally substituted with one or more groups selected from R 4  or Ht; C 2 -C 6  alkenyl, which is optionally substituted with one or more groups selected from R 4  or Ht; C 3 -C 6  saturated carbocycle, which is optionally substituted with one or more groups selected from R 4  or Ht; or C 5 -C 6  unsaturated carbocycle, which is optionally substituted with one or more groups selected from R 4  or Ht;  
 each R 4  is independently selected from —OR 2 , —SR 2 , —C(O)—NHR 2 , —S(O) 2 —NHR 2 , halo, —NR 2 —C(O)—R 2 , —N(R 2 ) 2  or —CN;  
 each R −  is independently selected from hydrogen,  
                     
 wherein each M is independently selected from H, Li, Na, K, Mg, Ca, Ba, —N(R 2 ) 4  C 1 -C 12 -alkyl, C 2 -C 2 -alkenyl, or —R 6 ; wherein 1 to 4 —CH 2  radicals of the alkyl or alkenyl group, other than the —CH 2  that is bound to Z, is optionally replaced by a heteroatom group selected from O, S, S(O), S(O 2 ), or N(R 2 ); and wherein any hydrogen in said alkyl, alkenyl or R 6  is optionally replaced with a substituent selected from oxo, —OR 2 , —R 2 , N(R 2 ) 2 , N(R 2 ) 3 , R 2 OH, —CN, —CO 2 R 2 , —C(O)—N(R 2 ) 2 , S(O) 2 —N(R 2 ) 2 , N(R 2 )—C(O)—R 2 , C(O)R − , —S(O) n —R 2 , OCF 3 , —S(O) n —R 6 , N(R 2 )—S(O) 2 (R 2 ), halo, —CF 3 , or —NO 3 ;  
 M′ is H, C 2 -C 2 -alkyl, C 2 -C 12 -alkenyl, or —R 6 ; wherein 1 to 4 —CH 2  radicals of the alkyl or alkenyl group is optionally replaced by a heteroatom group selected from O, S, S(O), S(O 2 ), or N(R 2 ); and wherein any hydrogen in said alkyl, alkenyl or R 6  is optionally replaced with a substituent selected from oxo, —OR 2 , —R 2 , —N(R 2 ), N(R 2 ) 3 , —R 2 OH, —CN, —CO 2 R 2 , —C(O)—N(R 2 ) 2 , —S(O) 2 —N(R 2 ) 2 , —N(R 2 )—C(O)—R 2 , —C(O)R 2 , —S(O) n —R 6 , —OCF 3 , —S(O) n —R 6 , —N(R 2 )—S(O) 2 (R 2 ), halo, —CF 3 , or —NO 2 ;  
 Z is O, S, N(R 2 ) 2 , or, when M is not present, H.  
 Y is P or S;  
 X is Q or S;  
 R 9  is C(R 2 ) 2 , O or N(R 2 ); and wherein when Y is S, Z is not S;  
 R 6  is a 5-6 membered saturated, partially saturated or unsaturated carbocyclic or heterocyclic ring system, or an 8-10 membered saturated, partially saturated or unsaturated bicyclic ring system; wherein any of said heterocyclic ring systems contains one or more heteroatoms selected from O, N, S, S(O) n  or N(R 2 ); and wherein any of said ring systems optionally contains 1 to 4 substituents independently selected from OH, C 1 -C 4  alkyl, O—C 1 -C 4  alkyl or O—C(O)—C 1 -C 4  alkyl;  
 R 8  is selected from C 1 -C 8  alkyl, C 3 -C 7  alkyl or cyano substituted C 2 -C 6  alkenyl; and  
 R 10  is selected from C 1 -C 8  alkyl, C 2 -C 6  alkenyl, C 6 -C 14  aryl or Ht, wherein R 10  optionally contains up to three substituents independently selected from —R 3 , —CN, —SR 5 , —SOR 5 , —SO 2 R 5 , —SR—NR 5 —C(O)R 6 , —NR 5 —(SO 2 )R 5 , —C(O)N(R 5 ) 2 , —C(S)N(R 5 ) 2 , —S(O) 2 N(R 5 ) 2 , —C(O)R 6 , —C(S)R 6 , —N(R 5 ) 2 , —NR 5 —C(O)R 5 , —NR 5 —C(O)OR 5 , —NR 5 —C(O)N(R 5 ) 2 , —NR 5 —C(S)R 5 , —NR 5 —C(S)OR 5 , —NR 5 —C(S)N(R 5 ) 2 , —NR 5 —C[═N(R 5 )]-N(R 5 ) 2 , —NH—C[═N—NO 2 ]—NH 2 , —NH—C[═N—NO 2 ]—OR 5 , —N(R 8 ) 2 —C(O)R 8 , —NH—C[═N—NO 2 ]—NH 2 , —NH—C[═N—NO 2 ]—OR 5 , —N(R 8 ) 2 —C(O)R 8 , —OC(O)R 6 , —OC(O)N(R 5 ) 2 , —OC(S)N(R 5 ) 2 , wherein any one of the —CH 2  groups of said alkyl or alkenyl chains of R 10  may be optionally replaced by O, S, SO, SO 2 , C(O) or NR 5 ;  
 wherein each R 5  is independently selected from hydrogen, C 1 -C 8  alkyl, C 2 -C 8  alkenyl, C 2 -C 8  alkynyl or Ht, wherein each R 5 , except for hydrogen, is optionally substituted with —CF3, —PO 3 R 3 , azido or halo;  
 or a pharmaceutically acceptable derivative thereof.  
 
     
     
         2 . The compound according to  claim 1 , wherein at least one R 7  is selected from:  
       
         
           
           
               
               
           
         
         
           
           
               
               
           
         
       
     
     
         3 . A compound of formula (II):  
       
         
           
           
               
               
           
         
       
       wherein A, R 7 , D′ and E are as defined in  claim 1;  or a pharmaceutically acceptable derivative thereof.  
     
     
         4 . A compound of formula (III):  
       
         
           
           
               
               
           
         
       
       wherein Ht, x, R 3 , R 7 , D′ and E are as defined in  claim 1;  or a pharmaceutically acceptable derivative thereof.  
     
     
         5 . A compound of formula (IV):  
       
         
           
           
               
               
           
         
       
       wherein A, R 3 , R 7 , D′ and E are as defined in  claim 1;  or a pharmaceutically acceptable derivative thereof.  
     
     
         6 . The compound according to  claim 3 , wherein: 
 A is —C(O)Ht;    D′ is —R 10 ;    E is C 6 -C 10  aryl optionally substituted with one or more substituents selected from oxo, —OR 3 , SR 2 , —R 3 , —N(R 2 ) 2 , —R 2 —OH, —CN, —CO 2 R 2 , —C(O)—N(R 2 ) 2 , —S(O) 2 —N(R 2 ) 2 , —N(R 2 )—C(O)—R 2 , —C(O)—R 2 , —S(O) n —R 2 , —OCF 3 , —S(O) n -Q, methylenedioxy, —N(R 2 )—S(O) 2 (R 2 ), halo, —CF 3 , —NO 2 , Q, —OQ, —OR 7 , —SR 7 , —R 7 , —N(R 2 )(R − ) or —N(R 7 ) 2 ; or a 5-membered heterocyclic ring containing one S and optionally containing N as an additional heteroatom, wherein said heterocyclic ring is optionally substituted with one to two groups independently selected from —CH 3 , R 4 , or Ht.    
     
     
         7 . The compound according to  claim 3 , wherein: 
 E is a 5-membered heterocyclic ring containing one S and optionally containing N as an additional heteroatom, wherein said heterocyclic ring is optionally substituted with one to two groups independently selected from —CH 3 , R 4 , or Ht.    
     
     
         8 . The compound according to  claim 3 , wherein: 
 R 7  in —OR 7  group shown in formula II is —PO(OM) 2  or C(O)CH 2 OCH 2 CH 2 OCH 2 CH 2 OCH 3  and both R − in —N(R 7 ) 7  are H; or R − in —OR 7  group shown in formula II is C(O)CH 2 OCH 2 CH 2 OCH 3 , one R − in —N(R 7 ) 2  is C(O)CH 2 OCH 2 CH 2 OCH 3  and the other is H; and    wherein M is H, Li, Na, K or C 1 -C 4  alkyl.    
     
     
         9 . A compound according to  claim 1 , having formula (V):  
       
         
           
           
               
               
           
         
       
       wherein A, R 7 , R 10  and E are as defined in  claim 1;  or a pharmaceutically acceptable derivative thereof.  
     
     
         10 . A compound of formula (VI):  
       
         
           
           
               
               
           
         
       
       wherein: 
 R 11  and R 7  are as defined in  claim 1;   
 E is C 6 -C 14  aryl, optionally substituted with one or more groups selected from the group consisting of nitro, oxo, alkoxy, amino, hydroxyamino; heterocyclcyl, optionally substituted with one or more groups selected from the group consisting of nitro, oxo, alkoxy, amino, hydroxyamino or —N(CO)OCH 3 ;  
 or a pharmaceutically acceptable derivative thereof.  
 
     
     
         11 . A compound of formula (VII):  
       
         
           
           
               
               
           
         
       
       wherein A, E, R 7  and R 10  are as defined in  claim 1;  or a pharmaceutically acceptable derivative thereof.  
     
     
         12 . A compound of formula (VIII):  
       
         
           
           
               
               
           
         
         wherein A, R 1 , R 3 , R 7  and E are as defined in  claim 1;   
         or a pharmaceutically acceptable salt thereof.  
       
     
     
         13 . A compound selected from:  
       
         
           
           
               
               
           
         
         
           
           
               
               
           
         
       
       wherein R 10  is selected from isopropyl or cyclopentyl; R 11  is selected from NHR 7  or OR 7 ; x, R 7  and G are as defined in  claim 1;  and X −  is a pharmaceutically acceptable counterion.  
     
     
         14 . A compound selected from: 
 (3R, 3aS, 6aR)hexahydrofuro[2,3-b]furan-3-yl N-((1S,2R)-1-benzyl-3-(cyclopentyloxy) [(3-[2-(dimethylamino)ethyl]aminophenyl)sulfonyl]amino-2-hydroxypropyl)carbamate;    (3S, 3aR, 6aS)hexahydrofuro[2,3-b]furan-3-yl N-((1S, 2R)-1-benzyl-3-(cyclopentyloxy) [(3-[2-(dimethylamino)ethyl]aminophenyl) sulfonyl]amino-2-hydroxypropyl)carbamate;    (3R,3aS,6aR)Hexahydrofuro[2,3-b]furan-3-yl-N-((1S,2R)-1-benzyl -3-(cyclopentyloxy)(2-[(methylsulfonyl)amino]benzimidazol-5-ylsulfonyl)amino-2-hydroxypropyl)carbamate;    (3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl N-(1S,2R)-3-[[(3-N-methylaminophenyl)sulfonyl](cyclopentyloxy)amino]-1-benzyl -2-hydroxypropylcarbamate;    1,3-Dioxan-5-yl N-(1S,2R)-1-benzyl-3-[(cyclopentyloxy)(2-{(methoxycarbonyl)amino]-1H-benzimidazol-5-ylsulfonyl)amino]-2-hydroxypropylcarbamate;    (3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl N-(1S,2R)-1-benzyl -2-hydroxy-3-[[(4-methoxyphenyl)sulfonyl](tetrahydro-2H -pyran-4-yloxy)amino]propylcarbamate;    (3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl N-(1S, 2R)-3-[[(3-aminophenyl)sulfonyl](cyclopentyloxy)amino]-1-benzyl-2-hydroxypropylcarbamate;    (3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl N-[(1S,2R)-1-benzyl -3-((cyclopentyloxy)[3-(2-[methoxy(methyl)amino]-2-oxoethylamino)phenyl]sulfonylamino)-2-hydroxypropyl]carbamate;    (3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl N-[(1S,2R)-1-benzyl-4-(cyclopentyloxy)-2-hydroxy-4-(6-quinoxalinyl sulfonyl)butyl]carbamate;    (3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl N-((1S,2R)-1-benzyl-3-(cyclopentyloxy)[(4-methoxyphenyl)sulfonyl]amino-2-hydroxypropyl)carbamate;    (3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl N-[(1S,2R)-1-benzyl-3-((cyclopentyloxy)[3-(2-[(methylsulfonyl)amino]ethylamino)phenyl]sulfonylamino)-2-hydroxypropyl]carbamate;    (3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl N-(1S,2R)-3-[[(3-N-methylaminophenyl)sulfonyl](cyclopentyloxy)amino]-1-benzyl-2-hydroxypropylcarbamate, phosphate ester;    (3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl N-(1S,2R)-3[[(3-aminophenyl)sulfonyl](cyclopentyloxy)amino]-1-benzyl-2-hydroxypropylcarbamate phosphate ester;    (3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl N-(1S,2R)-3-[[(4-aminophenyl)sulfonyl](cyclopentyloxy)amino]-1-benzyl-2-hydroxypropyl carbamate;    (3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl(1S,2R)-1-benzyl -3-{(1-ethylpropoxy)[(4-hydroxyphenyl)sulfonyl]amino}2-hydroxypropylcarbamate;    (3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl(1S,2R)-3[(1,3-benzodioxol-5-ylsulfonyl)(1-ethylpropoxy)amino]-1-benzyl -2-hydroxypropylcarbamate;    (3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl N-[(1S,2R)-3-[(1,3-benzodioxol-5-ylsulfonyl)(cyclopentyloxy)amino]-1-benzyl -2-(phosphonooxy)propyl]carbamate;    (3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl(1S,2R)-3-(1,3-benzodioxol-5-ylsulfonyl)(cyclohexyloxy)amino]-1-benzyl-2-hydroxypropylcarbamate;    (3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl 3-[(1,3-benzodioxol-5-ylsulfonyl)(tetrahydro-2H-pyran-4-yloxy)amino]-1-benzyl-2-hydroxypropylcarbamate;    (3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl N-[(1S, 2R)-3-[(1,3-benzodioxol-5-ylsulfonyl)(cyclopentyloxy)amino]-1-benzyl -2-(phosphonooxy)propyl]carbamate;    or a pharmaceutically acceptable derivative thereof.    
     
     
         15 . The compound according to  claim 1  wherein said compound has a molecular weight less than or equal to about 700 g/mol.  
     
     
         16 . The compound according to  claim 15  wherein said compound has a molecular weight less than or equal to about 600 g/mol.  
     
     
         17 . A pharmaceutical composition comprising an effective antiviral amount of a compound according to any one of claims  1 - 14  or a pharmaceutically acceptable derivative thereof together with a pharmaceutically acceptable carrier therefore.  
     
     
         18 . The pharmaceutical composition according to  claim 17 , further comprising an antiviral agent other than a compound according to claims  1 - 14 .  
     
     
         19 . A pharmaceutical composition according to  claim 17  or  18  in the form of a tablet or capsule.  
     
     
         20 . A method of treating a virus infection in a human comprising administering to said human an effective antiviral treatment amount of a compound according to any one of claims  1 - 13  or a pharmaceutically acceptable derivative thereof.  
     
     
         21 . The method according to  claim 20  wherein the virus infection is an HIV infection.  
     
     
         22 . The method according to  claim 20  or  21  wherein said step of administering comprises oral administration or administration by injection.  
     
     
         23 . Use of a compound according to any of claims  1 - 14  for the manufacture of a medicament for the treatment or prophylaxis of a viral infection.  
     
     
         24 . Use of a compound according to any of claims  1 - 14  or a formulation according to  claim 17  for use in medical therapy.