US2010022467A1PendingUtilityA1

Anti-cancer phosphonate analogs

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Assignee: BOOJAMRA CONSTANTINE GPriority: Apr 25, 2003Filed: Sep 2, 2008Published: Jan 28, 2010
Est. expiryApr 25, 2023(expired)· nominal 20-yr term from priority
A61P 35/00A61K 31/7076A61K 31/675A61K 31/7072A61K 47/548C07H 19/04
57
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Claims

Abstract

The invention is related to phosphorus substituted anti-cancer compounds, compositions containing such compounds, and therapeutic methods that include the administration of such compounds, as well as to processes and intermediates useful for preparing such compounds.

Claims

exact text as granted — not AI-modified
1 . A conjugate of the formula:
   [DRUG]-(A 0 ) nn ;   or a pharmaceutically acceptable salt or solvate thereof;   
     wherein:
 DRUG is a compound of formula 557: 
 
     
       
         
         
             
             
         
       
     
     wherein:
 nn is 1, 2 or 3; 
 A 0  is A 1 , A 2  or W 3  with the proviso that the conjugate includes at least one A 1 ; 
 
     
       
         
         
             
             
         
       
       Y 1  is independently O, S, N(R x ), N(O)(R x ), N(OR x ), N(O)(OR x ), or N(N(R x )(R x )); 
       Y 2  is independently a bond, O, N(R x ), N(O)(R x ), N(OR x ), N(O)(OR x ), N(N(R x )(R x )), —S(O) M2 —, or —S(O) M2 —S(O) M2 —; and when Y 2  joins two phosphorous atoms Y 2  can also be C(R 2 )(R 2 ); 
       R x  is independently H, R 1 , R 2 , W 3 , a protecting group, or the formula: 
     
     
       
         
         
             
             
         
       
       wherein: 
       R y  is independently H, W 3 , R 2  or a protecting group; 
       R 1  is independently H or alkyl of 1 to 18 carbon atoms; 
       R 2  is independently H, R 1 , R 3  or R 4  wherein each R 4  is independently substituted with 0 to 3 R 3  groups or taken together at a carbon atom, two R 2  groups form a ring of 3 to 8 carbons and the ring may be substituted with 0 to 3 R 3  groups; 
       R 3  is R 3a , R 3b , R 3c  or R 3d , provided that when R 3  is bound to a heteroatom, then R 3  is R 3c  or R 3d ; 
       R 3a  is F, Cl, Br, I, —CN, N 3  or —NO 2 ; 
       R 3b  is Y 1 ; 
       R 3c  is —R x , —N(R x )(R x ), —SR x , —S(O)R x , —S(O) 2 R x , —S(O)(OR x ), —S(O) 2 (OR x ), —OC(Y 1 )R x , —OC(Y 1 )OR x , —OC(Y 1 )(N(R x )(R x )), —SC(Y 1 )R x , —SC(Y 1 )OR x , —SC(Y 1 )(N(R x )(R x )), —N(R x )C(Y 1 )R x , —N(R x )C(Y 1 )OR x , or —N(R x )C(Y 1 )(N(R x )(R x )); 
       R 3d  is —C(Y 1 )R x , —C(Y 1 )OR x  or —C(Y 1 )(N(R x )(R x )); 
       R 4  is an alkyl of 1 to 18 carbon atoms, alkenyl of 2 to 18 carbon atoms, or alkynyl of 2 to 18 carbon atoms; 
       R 5  is R 4  wherein each R 4  is substituted with 0 to 3 R 3  groups; 
       W 3  is W 4  or W 5 ; 
       W 4  is R 5 , —C(Y 1 )R 5 , —C(Y 1 )W 5 , —SO M2 R 5 , or —SO M2 W 5 ; 
       W 5  is carbocycle wherein W 5  is independently substituted with 0 to 3 R 2  groups; 
       W 6  is W 3  independently substituted with 1, 2, or 3 A 3  groups; 
       M2 is 0, 1 or 2; 
       M12a is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12; 
       M12b is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12; 
       M1a, M1c, and M1d are independently 0 or 1; and 
       M12c is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12. 
     
   
   
       2 . The conjugate of  claim 1  that is of formula 211 or 212: 
     
       
         
         
             
             
         
       
       or a pharmaceutically acceptable salt or solvate thereof; 
     
     wherein:
 one A 0  is A 1 . 
 
   
   
       3 . The conjugate of  claim 1  wherein each A 3  is of the formula: 
     
       
         
         
             
             
         
       
     
   
   
       4 . The conjugate of  claim 1  wherein each A 3  is of the formula: 
     
       
         
         
             
             
         
       
     
     wherein the phenyl carbocycle is substituted with 0, 1, 2, or 3 R 2  groups. 
   
   
       5 . The conjugate of  claim 1  wherein each A 3  is of the formula: 
     
       
         
         
             
             
         
       
     
     wherein:
 Y 1a  is O or S; and 
 Y 2a  is O, N(R 2 ) or S. 
 
   
   
       6 . The conjugate of  claim 1  wherein A 0  is of the formula: 
     
       
         
         
             
             
         
       
     
     wherein each R is independently alkyl. 
   
   
       7 . The conjugate of  claim 2  wherein each A 3  is of the formula: 
     
       
         
         
             
             
         
       
     
   
   
       8 . The conjugate of  claim 2  wherein each A 3  is of the formula: 
     
       
         
         
             
             
         
       
     
     wherein the phenyl carbocycle is substituted with 0, 1, 2, or 3 R 2  groups. 
   
   
       9 . The conjugate of  claim 2  wherein each A 3  is of the formula: 
     
       
         
         
             
             
         
       
     
     wherein:
 Y 1a  is O or S; and 
 Y 2a  is O, N(R 2 ) or S. 
 
   
   
       10 . The conjugate of  claim 2  wherein A 0  is of the formula: 
     
       
         
         
             
             
         
       
     
     wherein each R is independently alkyl. 
   
   
       11 . A pharmaceutical composition comprising a pharmaceutical excipient and a conjugate as described in  claim 1 , or a pharmaceutically acceptable salt or solvate thereof. 
   
   
       12 . A pharmaceutical composition comprising a pharmaceutical excipient and a conjugate as described in  claim 2 , or a pharmaceutically acceptable salt or solvate thereof.

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