US2014315880A1PendingUtilityA1

3,6-diazabicyclo[3.1.1]heptaines as neuronal nicotinic acetycholine receptor ligands

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Assignee: TARGACEPT INCPriority: Dec 7, 2009Filed: Jul 1, 2014Published: Oct 23, 2014
Est. expiryDec 7, 2029(~3.4 yrs left)· nominal 20-yr term from priority
A61P 43/00A61P 9/10A61P 25/00A61P 25/02A61P 25/08A61P 25/16A61P 25/32A61P 25/22A61P 25/28A61P 25/34A61P 25/18A61P 25/30A61P 25/24A61P 25/04A61P 25/14A61P 21/02C07D 487/08C07D 471/08A61K 31/4995
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Claims

Abstract

The present invention relates to compounds that bind to and modulate the activity of neuronal nicotinic acetylcholine receptors, to processes for preparing these compounds, to pharmaceutical compositions containing these compounds, and to methods of using these compounds for treating a wide variety of conditions and disorders, including those associated with dysfunction of the central nervous system (CNS).

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A compound of Formula I: 
       
         
           
           
               
               
           
         
         wherein:
 each m is identical and is 0 or 1; 
 each n is identical and is 0 or 1; 
 when each m is 0, then each n is 1; 
 when each m is 1, then each n is 0; 
 
         R 1  is
 —C(O)—R 3A , 
 —C(O)O—R 3B , 
 
         R 2  is H; 
         R 3A  is methyl, propyl, butyl, pentyl, hexyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, cycloalkynyl, aryl, heteroaryl, or heterocyclic; 
         R 3B  is methyl, ethyl, propyl, n-butyl, isobutyl, sec-butyl, pentyl, hexyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, cycloalkynyl, aryl, heteroaryl, or heterocyclic; 
         each R 3A  and R 3B  individually may be optionally substituted with one or more alkyl, alkenyl, alkynyl, aryl, aryloxy, amino, amido, heteroaryl, halogen, hydroxyl, alkoxy, cycloalkyl, cycloalkenyl, cycloalkynyl, heterocyclic, or alkylamido substituents; 
         or a pharmaceutically acceptable salt thereof. 
       
     
     
         2 . The compound according to  claim 1 , wherein m is 0. 
     
     
         3 . The compound according to  claim 1 , wherein m is 1. 
     
     
         4 . A pharmaceutical composition comprising a compound as claimed in  claim 1 , and a pharmaceutically acceptable carrier.

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