IP Library Granted Patent US 7,786,171
Granted Patent B2
US 7,786,171 · App. 12/412,110 · Granted Aug 31, 2010

Amide derivatives as positive allosteric modulators and methods of use thereof

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Quick Facts
Patent No.
US 7,786,171
App. No.
12/412,110
Granted
Aug 31, 2010
Kind
B2
Abstract

The invention relates to novel amide derivatives that are positive allosteric modulators of neuronal nicotinic receptors, compositions comprising the same, processes for preparing such compounds, and methods for using such compounds and compositions.

Claims (29)

1. A compound of formula (I):

wherein,

A is —C(O)NH—;

R a , R b , and R c are independently hydrogen, alkenyl, alkoxy, alkoxycarbonyl, alkyl, alkylcarbonyl, alkylsulfonyl, alkylthio, cyano, haloalkoxy, haloalkyl, or halogen;

R x at each occurrence is independently acyloxy, alkoxy, alkyl, haloalkyl, halogen, or hydroxy;

n is 0, 1, 2, 3, or 4;

R 1 is hydrogen or halogen;

R 2 and R 3 are independently hydrogen, alkenyl, alkoxy, alkoxycarbonyl, alkyl, alkylcarbonyl, alkylsulfonyl, alkylthio, cyano, haloalkoxy, haloalkyl, halogen or NR 5 R 6 , provided that at least one of R 2 or R 3 is NR 5 R 6 :

R 5 and R 6 are independently hydrogen, alkenyl, alkoxyalkyl, alkoxycarbonyl, alkyl, alkylcarbonyl, alkylsulfonyl, arylalkyl, cycloalkyl, cycloalkylalkyl, haloalkyl, heteroarylalkyl, heterocycle, or heterocyclealkyl;

or a pharmaceutically acceptable salt thereof.

2. The compound of claim 1 , wherein R 1 is hydrogen or fluorine, or a pharmaceutically acceptable salt thereof.

3. The compound of claim 1 , wherein R 5 and R 6 are independently selected from hydrogen, alkyl, alkoxycarbonyl, alkylcarbonyl, alkylsulfonyl, arylalkyl, cycloalkyl, cycloalkylalkyl, haloalkyl, and heteroarylalkyl, or a pharmaceutically acceptable salt thereof.

4. The compound of claim 1 , wherein n is 0, and R a , R b , and R c are hydrogen, or a pharmaceutically acceptable salt thereof.

5. The compound of claim 1 , selected from the group consisting of:

(i.e. compounds from N-[3-(1H-pyrrol-1-yl)benzyl]-4-[(trifluoromethyl)thio]benzamide through N-[4-(4-methyl-1,4-diazepan-1-yl)benzyl]-4-[(trifluoromethyl)thio]benzamide);

N-[4-(acetylamino)benzyl]-4-[(trifluoromethyl)thio]benzamide;

N-[4-(diethylamino)benzyl]-4-[(trifluoromethyl)thio]benzamide;

N-{3-[(methylsulfonyl)amino]benzyl}-4-[(trifluoromethyl)thio]benzamide;

N-[3-(methylamino)benzyl]-4-[(trifluoromethyl)thio]benzamide;

N-{4-[(methylsulfonyl)amino]benzyl}-4-[(trifluoromethyl)thio]benzamide;

N-[3-(dimethylamino)benzyl]-4-[(trifluoromethyl)thio]benzamide;

N-{3-[acetyl(methyl)amino]benzyl}-4-[(trifluoromethyl)thio]benzamide;

N-[4-(dimethylamino)benzyl]-4-[(trifluoromethyl)thio]benzamide;

N-(4-aminobenzyl)-4-[(trifluoromethyl)thio]benzamide;

N-[4-(methylamino)benzyl]-4-[(trifluoromethyl)thio]benzamide;

4-[(difluoromethyl)thio]-N-[4-(dimethylamino)benzyl]benzamide; and

4-[(difluoromethyl)thio]-N-[4-(methylamino)benzyl]benzamide;

or a pharmaceutically acceptable salt thereof.

6. A pharmaceutical composition comprising a therapeutically effective amount of the compound of claim 1 or a pharmaceutically acceptable salt thereof, in combination with a pharmaceutically acceptable carrier.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 17, 2013
From: ABBOTT LABORATORIES
To: ABBVIE INC.
Reel/Frame 030237/0597 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 26, 2009
From: SCHRIMPF, MICHAEL R.; MORTELL, KATHLEEN H.; NERSESIAN, DIANA L.; LEE, CHIH-HUNG; CLAPHAM, BRUCE
To: ABBOTT LABORATORIES
Reel/Frame 022457/0764 →