US2008280894A1PendingUtilityA1

DIHYDRO[1,4]OXAZINO[2,3,4-hi]INDAZOLE DERIVATIVES AS 5-HYDROXYTRYPTAMINE-6 LIGANDS

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Assignee: WYETH CORPPriority: Apr 12, 2006Filed: Jul 15, 2008Published: Nov 13, 2008
Est. expiryApr 12, 2026(expired)· nominal 20-yr term from priority
C07D 491/06A61P 25/00A61P 25/28
60
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Claims

Abstract

The present invention provides a compound of formula I and the use thereof for the treatment of a central nervous system disorder related to or affected by the 5-HT6 receptor.

Claims

exact text as granted — not AI-modified
1 . A method of treating a central nervous system disorder relating to decreased cognition and memory in an Alzheimer's patient in need thereof, which method comprises providing to said patient a therapeutically effective amount of a compound of formula I 
     
       
         
         
             
             
         
       
     
     wherein
 R 1  is H, halogen, CN, NO 2 , OR 7 , alkyl or haloalkyl; 
 R 2  is an alkyl, cycloalkyl, aryl or heteroaryl group each group optionally substituted or an optionally substituted 8- to 13-membered bicyclic or tricyclic ring system having a N atom at the bridgehead and optionally containing 1, 2 or 3 additional heteroatoms selected from N, O or S; 
 R 3  and R 4  are each independently H, or an optionally substituted alkyl group; 
 n is an integer of 1, 2, 3, 4, or 5; 
 R 5  and R 6  are each independently H or an alkyl, alkenyl, alkynyl or cycloalkyl, group each group optionally substituted or R 5  and R 6  may be taken together with the atom to which they are attached to form an optionally substituted 3- to 7-membered ring optionally containing an additional heteroatom selected from N, O or S; and 
 R 7  is H, alkyl or haloalkyl; or 
 
     a stereoisomer thereof or a pharmaceutically acceptable salt thereof; 
     wherein the optional substituents are selected from the group consisting of halogen atoms, nitro, cyano, thiocyanato, hydroxyl, alkyl, haloalkyl, alkoxy, haloalkoxy, amino, alkylamino, dialkylamino, formyl, alkoxycarbonyl, carboxyl, alkanoyl, alkylthio, alkylsulphinyl, alkylsulphonyl, carbamoyl, alkylamido, phenyl, phenoxy, benzyl, benzyloxy, heterocyclyl and cycloalkyl groups. 
   
   
       2 . The method according to  claim 1  comprising enhancing cognition and memory in said Alzheimer's patient. 
   
   
       3 . The method according to  claim 1  wherein n is 1. 
   
   
       4 . The method according to  claim 3  wherein R 2  is an optionally substituted aryl or heteroaryl group or an optionally substituted 8- to 13-membered bicyclic or tricyclic ring system having a N atom at the bridgehead and optionally containing 1, 2 or 3 additional heteroatoms selected from N, O or S. 
   
   
       5 . The method according to  claim 4  wherein R 5  and R 6  are each independently H or alkyl or R 5  and R 6  are taken together with the atom to which they are attached to form an optionally substituted 3- to 7-membered ring. 
   
   
       6 . The method according to  claim 3  wherein R 1  is H, halogen or C 1 -C 3  alkyl. 
   
   
       7 . The method according to  claim 3  wherein R 2  is an optionally substituted aryl or heteroaryl group and R 3  and R 4  are H. 
   
   
       8 . A method of enhancing cognition and memory related to Alzheimer's disease in a patient in need thereof which comprises providing to said patient a therapeutically effective amount of a compound of formula I 
     
       
         
         
             
             
         
       
     
     wherein
 R 1  is H, halogen, CN, NO 2 , OR 7 , alkyl or haloalkyl; 
 R 2  is an alkyl, cycloalkyl, aryl or heteroaryl group each group optionally substituted or an optionally substituted 8- to 13-membered bicyclic or tricyclic ring system having a N atom at the bridgehead and optionally containing 1, 2 or 3 additional heteroatoms selected from N, O or S; 
 R 3  and R 4  are each independently H, or an optionally substituted alkyl group; 
 n is an integer of 1, 2, 3, 4, or 5; 
 R 5  and R 6  are each independently H or an alkyl, alkenyl, alkynyl or cycloalkyl, group each group optionally substituted or R 5  and R 6  may be taken together with the atom to which they are attached to form an optionally substituted 3- to 7-membered ring optionally containing an additional heteroatom selected from N, O or S; and 
 R 7  is H, alkyl or haloalkyl; or 
 
     a stereoisomer thereof or a pharmaceutically acceptable salt thereof; 
     wherein the optional substituents are selected from the group consisting of halogen atoms, nitro, cyano, thiocyanato, hydroxyl, alkyl, haloalkyl, alkoxy, haloalkoxy, amino, alkylamino, dialkylamino, formyl, alkoxycarbonyl, carboxyl, alkanoyl, alkylthio, alkylsulphinyl, alkylsulphonyl, carbamoyl, alkylamido, phenyl, phenoxy, benzyl, benzyloxy, heterocyclyl and cycloalkyl groups. 
   
   
       9 . The method according to  claim 8  wherein n is 1. 
   
   
       10 . The method according to  claim 9  wherein R 2  is an optionally substituted aryl or heteroaryl group or an optionally substituted 8- to 13-membered bicyclic or tricyclic ring system having a N atom at the bridgehead and optionally containing 1, 2 or 3 additional heteroatoms selected from N, O or S. 
   
   
       11 . The method according to  claim 10  wherein R 5  and R 6  are each independently H or alkyl or R 5  and R 6  are taken together with the atom to which they are attached to form an optionally substituted 3- to 7-membered ring. 
   
   
       12 . The method according to  claim 9  wherein R 1  is H, halogen or C 1 -C 3  alkyl. 
   
   
       13 . The method according to  claim 9  wherein R 2  is an optionally substituted aryl or heteroaryl group and R 3  and R 4  are H. 
   
   
       14 . A method of treating Alzheimer's disease in a patient, which method comprises providing to said patient a therapeutically effective amount of a compound of formula I 
     
       
         
         
             
             
         
       
     
     wherein
 R 1  is H, halogen, CN, NO 2 , OR 7 , alkyl or haloalkyl; 
 R 2  is an alkyl, cycloalkyl, aryl or heteroaryl group each group optionally substituted or an optionally substituted 8- to 13-membered bicyclic or tricyclic ring system having a N atom at the bridgehead and optionally containing 1, 2 or 3 additional heteroatoms selected from N, O or S; 
 R 3  and R 4  are each independently H, or an optionally substituted alkyl group; 
 n is an integer of 1, 2, 3, 4, or 5; 
 R 5  and R 6  are each independently H or an alkyl, alkenyl, alkynyl or cycloalkyl, group each group optionally substituted or R 5  and R 6  may be taken together with the atom to which they are attached to form an optionally substituted 3- to 7-membered ring optionally containing an additional heteroatom selected from N, O or S; and 
 R 7  is H, alkyl or haloalkyl; or 
 
     a stereoisomer thereof or a pharmaceutically acceptable salt thereof; 
     wherein the optional substituents are selected from the group consisting of halogen atoms, nitro, cyano, thiocyanato, hydroxyl, alkyl, haloalkyl, alkoxy, haloalkoxy, amino, alkylamino, dialkylamino, formyl, alkoxycarbonyl, carboxyl, alkanoyl, alkylthio, alkylsulphinyl, alkylsulphonyl, carbamoyl, alkylamido, phenyl, phenoxy, benzyl, benzyloxy, heterocyclyl and cycloalkyl groups. 
   
   
       15 . The method according to  claim 14  comprising enhancing cognition and memory in said Alzheimer's patient. 
   
   
       16 . The method according to  claim 14  wherein n is 1. 
   
   
       17 . The method according to  claim 16  wherein R 2  is an optionally substituted aryl or heteroaryl group or an optionally substituted 8- to 13-membered bicyclic or tricyclic ring system having a N atom at the bridgehead and optionally containing 1, 2 or 3 additional heteroatoms selected from N, O or S. 
   
   
       18 . The method according to  claim 17  wherein R 5  and R 6  are each independently H or alkyl or R 5  and R 6  are taken together with the atom to which they are attached to form an optionally substituted 3- to 7-membered ring. 
   
   
       19 . The method according to  claim 16  wherein R 1  is H, halogen or C 1 -C 3  alkyl. 
   
   
       20 . The method according to  claim 16  wherein R 2  is an optionally substituted aryl or heteroaryl group and R 3  and R 4  are H.

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