Chemical compounds

Abstract

Pyrazole derivatives are described herein. The described invention also includes methods of making such pyrazole derivatives as well as methods of using the same in the treatment of diseases.

1 . A compound of Formula (I): 
       
         
           
           
               
               
           
         
       
       wherein:
 A is C 3 -C 7  cycloalkyl, aryl or heteroaryl, wherein said C 3 -C 7  cycloalkyl, aryl and heteroaryl is substituted with at least one independently selected R 2  group, and optionally further substituted; 
 D is hydrogen; 
 R is independently selected from C 1 -C 6  alkylene, C 2 -C 6  alkenylene, or C 2 -C 6  alkynylene, which alkylene, alkenylene, and alkynylene may optionally be substituted; 
 R 1  is independently selected from hydrogen, C 1 -C 6  alkyl, aryl, —RR 3 , —C(O)OR 4 , —C(O)NR 5 R 6 , and —C(O)R 4 , which alkyl and aryl may optionally be substituted; 
 R 2  is independently selected from —NR′″C(O)NR′″R″″, —NR′″—C(═N—CN)—NR′″R″″ or the structure: 
 
       
         
           
           
               
               
           
         
         R 3  is independently selected from hydrogen, halo, C 1 -C 6  alkyl, C 1 -C 6  haloalkyl, C 3 -C 7  cycloalkyl, C 1 -C 6  alkoxy, C 3 -C 7  cycloalkoxy, C 1 -C 6  haloalkoxy, aryl, aralkyl, aryloxy, heteroaryl, heterocyclyl, —CN, —NHC(O)R, —NHC(S)R 4 , —NR 5 R 6 , —RNR 5 R 6 , —SR 4 , —S(O)R 4 , —S(O) 2 R 4 , —R C (O)OR 4 , —C(O)OR 4 , —C(O)R 4 , —C(O)NR 5 R 6 , —NHS(O) 2 R 4 , —S(O) 2 NR 5 R 6 , or —NHC(═NH)R 4 , which alkyl, haloalkyl, cycloalkyl, alkoxy, cycloalkoxy, haloalkoxy, aryl, aralkyl, aryloxy, heteroaryl and heterocyclyl may optionally be substituted; 
         R 4  is independently selected from hydrogen, C 1 -C 6  alkyl, aryl, heteroaryl, heterocyclyl, —RR 3 , —NR′″R″″, or —NR′NR′″R″″, which alkyl, aryl, heteroaryl, and heterocyclyl may optionally be substituted; 
         R 5  is independently selected from hydrogen, C 1 -C 6  alkyl, C 3 -C 7  cycloalkyl, cyanoalkyl, —R′R″, aryl, aralkyl, heteroaryl, —NHC(O)OR′″, —R′NHC(O)OR′″, —R′NHC(O)NR′″R″″, or —R′C(O)OR′″, which alkyl, cycloalkyl, cyanoalkyl, aryl, aralkyl, and heteroaryl may optionally be substituted; 
         R 6  is independently selected from hydrogen, C 1 -C 6  alkyl, C 3 -C 7  cycloalkyl, cyanoalkyl, —R′R″, aryl, aralkyl, heteroaryl, —C(O)OR′″, or —R′C(O)NR′″R′″, which alkyl, cycloalkyl, cyanoalkyl, aryl, aralkyl, and heteroaryl may optionally be substituted; 
         R′ is independently selected from optionally substituted C 1 -C 4  alkylene; 
         R″ is independently selected from optionally substituted heteroalkyl or NR′″R″″; 
         R′″ is independently selected from hydrogen, C 1 -C 6  alkyl, aryl, aralkyl, heteroaryl, or C 3 -C 7  cycloalkyl, which alkyl, aryl, aralkyl, heteroaryl, and cycloalkyl may optionally be substituted; and 
         R″″ is independently selected from hydrogen, C 1 -C 6  alkyl, aryl, heteroaryl, or C 3 -C 7  cycloalkyl, which alkyl, aryl, heteroaryl, and cycloalkyl may optionally be substituted; 
       
       or a salt, solvate, or physiologically functional derivative thereof. 
     
     
         2 . A compound as claimed in  claim 1 , wherein A, said C 3 -C 7  cycloalkyl, aryl or heteroaryl is substituted with one R 2  group and optionally substituted with one or more groups other than R 2 ; or a salt, solvate, or physiologically functional derivative thereof. 
     
     
         3 . A compound as claimed in  claim 1 , wherein A is aryl or heteroaryl, substituted with at least one independently selected R 2  group and optionally further substituted; or a salt, solvate, or physiologically functional derivative thereof. 
     
     
         4 . A compound as claimed in  claim 1 , wherein R 2  is —NR′″C(O)NR′″R″″. 
     
     
         5 . A compound as claimed in  claim 1 , wherein R′″ is hydrogen. 
     
     
         6 . A compound as claimed in  claim 1 , wherein R″″ is aryl or heteroaryl, either optionally substituted. 
     
     
         7 . A compound as claimed in  claim 1 , wherein R 1  is H or optionally substituted C 1 -C 6  alkyl; or a salt, solvate, or physiologically functional derivative thereof. 
     
     
         8 . A compound as claimed in  claim 1 , which is: 
       -Amino-3-{4-[3-2-(fluoro-5-trifluoromethyl-phenyl)-ureido]-phenyl}-1H-pyrazole-4-carboxylic acid amide; 
       or a salt, solvate, or physiologically functional derivative thereof. 
     
     
         9 . A compound as claimed in  claim 1 , wherein A is phenyl substituted with at least one independently selected R 2  group and optionally further substituted; or a salt, solvate, or physiologically functional derivative thereof.