Beta3 adrenergic agonists

Abstract

The present invention relates to a β 3 adrenergic receptor agonist of formula I: or a pharmaceutical salt thereof; which is capable of increasing lipolysis and energy expenditure in cells and, therefore, is useful for treating Type II diabetes and/or obesity. The compound can also be used to lower triglyceride levels and cholesterol levels or raise high density lipoprotein levels or to decrease gut motility. In addition, the compound can be used to reduced neurogenic inflammation or as an antidepressant agent. Compositions and methods for the use of the compounds in the treatment of diabetes and obesity and for lowering triglyceride levels and cholesterol levels or raising high density lipoprotein levels or for decreasing gut motility are also disclosed.

1 . A compound of formula I:  
       
         
           
           
               
               
           
         
       
       wherein: 
 A 1 , A 2  and A 3  are carbon or nitrogen provided that only one of A 1 , A 2  and A 3  is nitrogen;  
 Het is an optionally substituted, optionally benzofused 5 or 6 membered heterocyclic ring;  
 R 1 , R 1a  and R 1b  are independently H, halo, hydroxy, C 1 -C 6  alkyl, C 1 -C 6  alkoxy, C 1 -C 4  haloalkyl, or SO 2 (C 1 -C 6  alkyl);  
 R 2  is H or C 1 -C 6  alkyl;  
 R 3  is H or C 1 -C 6  alkyl;  
 R 4  is H or C 1 -C 6  alkyl;  
 or R 3  and R 4  combine with the carbon to which both are attached to form a C 3 -C 6  cyclic ring;  
 or R 4  and X 1  combine with the carbon to which both are attached to form a C 3 -C 8  cyclic ring;  
 or R 4  combines with X 1 , the carbon to which both are attached, and the phenyl group to which X 1  is attached to form:  
                     
 wherein:  
 n and m are independently 0, 1, 2, or 3 provided that the sum of n+m is≦4 and that R 3  is H;  
 X is OCH 2 , SCH 2  or a bond;  
 X 1  is a bond or a C 1 -C 5  divalent hydrocarbon moiety;  
 X 2  is O, S, NH, NHSO 2 , SO 2 NH, CH 2  or a bond; and  
 X 3  is optionally substituted phenyl or an optionally substituted 5 or 6 membered heterocyclic ring; or a pharmaceutical salt thereof.  
 
     
     
         2 . The compound of  claim 1  wherein: 
 A 1 , A 2  and A 3  are carbon;  
 Het is optionally substituted one to three times independently with halo, hydroxy, oxo, cyano, nitro, phenyl, benzyl, C 1 -C 4  alkyl, C 1 -C 4  haloalkyl, C 1 -C 4  alkoxy, COR 8 , CO 2 R 8 , CONR 8 R 8 , NR 8 R 8 , NHCO(C 1 -C 4  alkyl), NHCO(phenyl), NHCO(benzyl), SR 8 , SO(C 1 -C 4  alkyl), SO 2 (C 1 -C 4  alkyl), SO 2 (NR 8 R 8 ), OCO(C 1 -C 4  alkyl), OCO 2 R 8  or OCONR 8 R 8    
 R 1 , R 1a  and R 1b  are independently H, halo, C 1 -C 4  alkyl, C 1 -C 4  alkoxy, C 1 -C 4  haloalkyl, or SO 2 (C 1 -C 4  alkyl);  
 R 2  is H or C 1 -C 4  alkyl;  
 R 3  and R 4  are independently H or C 1 -C 4  alkyl;  
 or R 3  and R 4  combine with the carbon to which both are attached to form a C 3 -C 6  cyclic ring;  
 or R 4  and X 1  combine with the carbon to which both are attached to form a C 3 -C 8  cyclic ring;  
 or R 4  combines with X 1 , the carbon to which both are attached, and the phenyl group to which X 1  is attached to form:  
                     
 X 3  is optionally substituted one to three times independently with halo, hydroxy, oxo, cyano, nitro, phenyl, benzyl, C 1 -C 4  alkyl, C 1 -C 4  haloalkyl, C 1 -C 4  alkoxy, COR 8 , CO 2 R 8 , CONR 8 R 8 , NR 8 R 8 , NHCO(C 1 -C 4  alkyl), NHCO(phenyl), NHCO(benzyl), SR 8 , SO(C 1 -C 4  alkyl), SO 2 (C 1 -C 4  alkyl), SO 2 (NR 8 R 8 ), OCO(C 1 -C 4  alkyl), OCO 2 R 8  or OCONR 8 R 8 ; and  
 R 8  is independently at each occurrence H or C 1 -C 4  alkyl; or a pharmaceutical salt thereof.  
 
     
     
         3 . The compound of  claim 2  of the formula:  
       
         
           
           
               
               
           
         
       
       wherein: 
 Het is selected from furan; isothiazole; isoxazole; oxazole; and thiophene; wherein said Het moieties are optionally substituted once with fluorine, methyl, cyano, SO 2 NH 2  or COCH 3 ;  
 R 3  and R 4  are independently H or methyl;  
 X 3  is phenyl, pyridyl or pyridazinyl wherein said X 3  moieties are substituted once or twice with chloro, cyano, CONH 2  or SO 2 CH 3 ; or a pharmaceutical salt thereof.  
 
     
     
         4 . The compound of  claim 3  wherein Het is thien-2-yl optionally substituted once with fluorine, methyl, cyano, SO 2 NH 2  or COCH 3 ; R 3  and R 4  are both methyl; and X 3  is phenyl or pyridyl wherein said X 3  moieties are substituted once with cyano or CONH 2 ; or a pharmaceutical salt thereof.  
     
     
         5 . The compound of  claim 4  wherein X 3  is pyridyl substituted once with cyano or CONH 2 ; or a pharmaceutical salt thereof.  
     
     
         6 . The compound of  claim 5  which is selected from the group consisting of:  
       
         
           
           
               
               
           
         
       
       or a pharmaceutical salt thereof.  
     
     
         7 . A compound of the formula:  
       
         
           
           
               
               
           
         
       
       or a pharmaceutical salt thereof.  
     
     
         8 . The compound of  claim 7  which is the hydrochloride salt.  
     
     
         9 . The compound of  claim 7  which is the hemi-fumarate, benzoate, salicylate or R-mandelate salt.  
     
     
         10 . Cancelled  
     
     
         11 . A method of treating obesity comprising administering to a patient in need thereof a compound of  claim 3 .  
     
     
         12 . A method of treating Type II Diabetes comprising administering to a patient in need thereof a compound of  claim 3 .  
     
     
         13 . Cancelled  
     
     
         14 . Cancelled  
     
     
         15 . A compound of formula II:  
       
         
           
           
               
               
           
         
       
       wherein: 
 A 1 , A 2  and A 3  are carbon or nitrogen provided that only one of A 1 , A 2  and A 3  is nitrogen;  
 Het is an optionally substituted, optionally benzofused 5 or 6 membered heterocyclic ring;  
 R 1  and R 1a  are independently H, halo, hydroxy, C 1 -C 6  alkyl, C 1 -C 6  alkoxy, C 1 -C 6  haloalkyl, or SO 2  (C 1 -C 6  alkyl); or a salt thereof.  
 
     
     
         16 . The compound of  claim 15  of the formula:  
       
         
           
           
               
               
           
         
       
       wherein: 
 Het is selected from benzothiophene; furan; isothiazole; isoxazole; oxazole; thiophene; and thiazole; wherein said Het moieties are optionally substituted once with fluorine, chlorine, methyl, cyano, SO 2 NH 2  or COCH 3 ; or a salt thereof.  
 
     
     
         17 . A process for preparing a compound of  claim 1  which comprises reacting a compound of formula II:  
       
         
           
           
               
               
           
         
       
       with a compound of formula III:  
       
         
           
           
               
               
           
         
       
       in the presence of a suitable solvent.  
     
     
         18 . A method of treating obesity comprising administering to a patient in need thereof a compound of  claim 7 .  
     
     
         19 . A method of treating obesity comprising administering to a patient in need thereof a compound of  claim 8 .  
     
     
         20 . A method of treating obesity comprising administering to a patient in need thereof a compound of  claim 9.