Piperidine sulphonamide derivatives

Abstract

The present invention relates to piperidine sulphonamide derivatives of formula wherein Ar 1 , Ar 2 , R 1 , R 2 , m and n are as defined in the description and claims, or pharmaceutically suitable acid addition salts thereof. The compounds of formula I are orexin receptor antagonists and the related compounds can be useful in the treatment of sleep apnea, narcolepsy, insomnia, parasomnia, jet lag syndrome, circadian rhythms disorder or sleep disorders associated with neurological diseases.

1 . A compound of formula I 
       
         
           
           
               
               
           
         
       
       wherein
 Ar 1  and Ar 2  are each independently unsubstituted or substituted aryl or heteroaryl; 
 R 1  and R 2  are each independently hydroxy, halogen, lower alkyl, lower alkyl substituted by halogen, lower alkoxy, lower alkoxy substituted by halogen or cyano; 
 m is 0, 1, 2 or 3; and 
 n is 2; 
 or pharmaceutically suitable acid addition salts thereof. 
 
     
     
         2 . The compound of  claim 1 , selected from the group consisting of
 [1-(2-methoxy-benzenesulfonyl)-piperidin-3-yl]-(2-phenyl-piperidin-1-yl)-methanone and   [1-(5-chloro-2-methoxy-benzenesulfonyl)-piperidin-3-yl]-(2-phenyl-piperidin-1-yl)-methanone.   
     
     
         3 . The compound of  claim 1 , wherein Ar 1  is phenyl. 
     
     
         4 . The compound of  claim 1 , wherein Ar 1  is heteroaryl. 
     
     
         5 . The compound of  claim 1 , wherein Ar 2  is phenyl. 
     
     
         6 . The compound of  claim 1 , wherein Ar 2  is heteroaryl. 
     
     
         7 . The compound of  claim 1 , wherein m is 0. 
     
     
         8 . The compound of  claim 1 , wherein m is 1. 
     
     
         9 . The compound of  claim 1 , wherein m is 2. 
     
     
         10 . The compound of  claim 1 , wherein m is 3. 
     
     
         11 . A pharmaceutical composition comprising a therapeutically effective amount of a compound of formula I 
       
         
           
           
               
               
           
         
       
       wherein
 Ar 1  and Ar 2  are each independently unsubstituted or substituted aryl or heteroaryl; 
 R 1  and R 2  are each independently hydroxy, halogen, lower alkyl, lower alkyl substituted by halogen, lower alkoxy, lower alkoxy substituted by halogen or cyano; 
 m is 0, 1, 2 or 3; and 
 n is 2; 
 or pharmaceutically suitable acid addition salts thereof and a pharmaceutically acceptable carrier.