IP Library Granted Patent US 8,815,869
Granted Patent B2
US 8,815,869 · App. 13/045,010 · Granted Aug 26, 2014

Lactam acetamides as calcium channel blockers

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Quick Facts
Patent No.
US 8,815,869
App. No.
13/045,010
Granted
Aug 26, 2014
Kind
B2
Abstract

The present application relates to calcium channel inhibitors containing compounds of formula (I) wherein Ar 1 , n, R 1 , X and Y are as defined in the specification. The present application also relates to compositions comprising such compounds, and methods of treating conditions and disorders using such compounds and compositions.

Claims (45)

1. A compound of formula (I):

or a pharmaceutically acceptable salt thereof, wherein

n is 2;

X is CH 2 ;

R 1 is hydrogen, alkyl, or G 1 ;

Ar 1 is aryl or heteroaryl; wherein Ar 1 is unsubstituted or further substituted with 1, 2, 3, 4, or 5 substituents independently selected from the group consisting of alkyl, alkenyl, alkynyl, halogen, —CN, —NO 2 , —OR a , —S(R c ), —S(O)(R c ), —S(O) 2 R c , —S(O) 2 N(R b ) 2 , —C(O)R b , —C(O)O(R b ), —C(O)N(R b ) 2 , —N(R b ) 2 , —N(R b )C(O)R b , —N(R b )C(O)O(R b ), —N(R b )S(O) 2 R c , haloalkyl, —(CR d R e ) m —OR a , —(CR d R e ) m —S(R c ), —(CR d R e ) m —S(O)(R c ), —(CR d R e ) m —S(O) 2 R c , —(CR d R e ) m —S(O) 2 N(R b ) 2 , —(CR d R e ) m —C(O)R b , —(CR d R e ) m —C(O)O(R b ), —(CR d R e ) m —C(O)N(R b ) 2 , —(CR d R e ) m —N(R b ) 2 , —(CR d R e ) m —N(R b )C(O)R b , —(CR d R e ) m —N(R b )C(O)O(R b ), and —(CR d R e ) m —N(R b )S(O) 2 R c ;

R a , at each occurrence, is independently hydrogen, alkyl, haloalkyl, or —(CR d R e ) m —O(alkyl);

R b , at each occurrence, is independently hydrogen, alkyl, haloalkyl, or G 1 ;

R c , at each occurrence, is independently alkyl or haloalkyl;

R d and R e , at each occurrence, are each independently hydrogen, halogen, alkyl, or haloalkyl;

m, at each occurrence, is independently 1, 2, 3, 4, 5, or 6;

Y is (i-a), (i-b), (i-c), (i-d), (i-e), (ii), (iii), (iv), (v), (vi), (vii), (viii), (ix), (x) or (xi):

x is 1, 2, or 3;

y at each occurrence, is independently 1 or 2;

z at each occurrence, is independently 0, 1, or 2;

Q is O, S, or CH 2 ;

R 2 , at each occurrence, is independently hydrogen or alkyl;

R 3 is hydrogen, alkyl, or G 1 ; and

G 1 , at each occurrence, is independently aryl, heteroaryl, heterocycle, cycloalkyl, or cycloalkenyl; wherein each G 1 is independently unsubstituted or further substituted with 1, 2, 3, 4, 5, or 6 substituents independently selected from the group consisting of alkyl, alkenyl, alkynyl, halogen, oxo, —CN, —NO 2 , —OR a , —S(R c ), —S(O)(R c ), —S(O) 2 R c , —S(O) 2 N(R b ) 2 , C(O)R b , —C(O)O(R b ), —C(O)N(R b ) 2 , —N(R b ) 2 , —N(R b )C(O)R b , —N(R b )C(O)O(R b ), —N(R b )S(O) 2 R c , haloalkyl, —(CR d R e ) m —OR a , —(CR d R e ) m —S(R c ), —(CR d R e ) m —S(O)(R c ), —(CR d R e ) m —S(O) 2 R c , —(CR d R e ) m —S(O) 2 N(R b ) 2 , —(CR d R e ) m —C(O)R b , —(CR d R e ) m —C(O)O(R b ), —(CR d R e ) m —C(O)N(R b ) 2 , —(CR d R e ) m —N(R b ) 2 , —(CR d R e ) m —N(R b )C(O)R b , —(CR d R e ) m —N(R b )C(O)O(R b ), and —(CR d R e ) m —N(R b )S(O) 2 R c .

2. The compound or salt according to claim 1 , wherein R 1 is G 1 .

3. The compound or salt according to claim 2 , wherein

Ar 1 is aryl, wherein Ar 1 is unsubstituted or further substituted with 1, 2, or 3, substituents independently selected from the group consisting of alkyl, alkenyl, alkynyl, halogen, —CN, —NO 2 , —OR a , —S(R c ), —S(O)(R c ), —S(O) 2 R c , —S(O) 2 N(R b ) 2 , —C(O)R b , —C(O)O(R b ), —C(O)N(R b ) 2 , —N(R b ) 2 , —N(R b )C(O)R b , —N(R b )C(O)O(R b ), —N(R b )S(O) 2 R c , haloalkyl, —(CR d R e ) m —OR a , —(CR d R e ) m —S(R c ), —(CR d R e ) m —S(O)(R c ), —(CR d R e ) m —S(O) 2 R c , —(CR d R e ) m —S(O) 2 N(R b ) 2 , —(CR d R e ) m —C(O)R b , —(CR d R e ) m —C(O)O(R b ), —(CR d R e ) m —C(O)N(R b ) 2 , —(CR d R e ) m —N(R b ) 2 , —(CR d R e ) m —N(R b )C(O)R b , —(CR d R e ) m —N(R b )C(O)O(R b ), and —(CR d R e ) m —N(R b )S(O) 2 R c ; and

R 1 is G 1 , and G 1 is aryl, wherein G 1 is unsubstituted or further substituted with 1, 2, or 3 substituents independently selected from the group consisting of alkyl, alkenyl, alkynyl, halogen, oxo, —CN, —NO 2 , —OR a , —S(R c ), —S(O)(R c ), —S(O) 2 R c , —S(O) 2 N(R b ) 2 , C(O)R b , —C(O)O(R b ), —C(O)N(R b ) 2 , —N(R b ) 2 , —N(R b )C(O)R b , —N(R b )C(O)O(R b ), —N(R b )S(O) 2 R c , haloalkyl, —(CR d R e ) m —OR a , —(CR d R e ) m —S(R c ), —(CR d R e ) m —S(O)(R c ), —(CR d R e ) m —S(O) 2 R c , —(CR d R e ) m —S(O) 2 N(R b ) 2 , —(CR d R e ) m —C(O)R b , —(CR d R e ) m —C(O)O(R b ), —(CR d R e ) m —C(O)N(R b ) 2 , —(CR d R e ) m —N(R b ) 2 , —(CR d R e ) m —N(R b )C(O)R b , —(CR d R e ) m —N(R b )C(O)O(R b ), and —(CR d R e ) m —N(R b )S(O) 2 R c .

4. The compound or salt according to claim 3 , wherein

Ar 1 is aryl, wherein Ar 1 is unsubstituted or further substituted with 1, 2, or 3, substituents independently selected from the group consisting of alkyl, alkenyl, alkynyl, halogen, —CN, —OR a , or haloalkyl;

R 1 is G 1 , and G 1 is aryl, wherein G 1 is unsubstituted or further substituted with 1, 2, or 3 substituents independently selected from the group consisting of alkyl, alkenyl, alkynyl, halogen, —CN, —OR a , or haloalkyl; and

Y is (i-a), (i-b), (i-c), (i-d), (i-e), (ii), (iii), (iv), (v), (vi), (vii), (viii), or (ix):

5. The compound or salt according to claim 1 , wherein the compound is selected from the group consisting of:

2-(2-oxo-3,3-diphenylpiperidin-1-yl)-N-piperidin-4-ylacetamide;

3,3-dimethyl-4-[(2-oxo-3,3-diphenylpiperidin-1--yl)acetyl]piperazin-2-one;

1-{2-[(4aS,7aS)-octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl]-2-oxoethyl}-3,3-diphenylpiperidin-2-one;

1-{2-[(4aR,7aR)-octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl]-2-oxoethyl}-3,3-diphenylpiperidin-2-one;

1-{2-[(4aS,7aS)-octahydro-1H-pyrrolo[3,4-b]pyridin-1-yl]-2-oxoethyl}-3,3-diphenylpiperidin-2-one;

1-(2-hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl-2-oxoethyl)-3,3-diphenylpiperidin-2-one;

1-[2-(2,7-diazaspiro[3.5]non-2-yl)-2-oxoethyl]-3,3-diphenylpiperidin-2-one;

2-(2-oxo-3,3-diphenylpiperidin-1-yl)-N-[(2R)-pyrrolidin-2-ylmethyl]acetamide;

2-(2-oxo-3,3-diphenylpiperidin-1-yl)-N-[(2S)-pyrrolidin-2-ylmethyl]acetamide;

4-[(2-oxo-3,3-diphenylpiperidin-1-yl)acetyl]piperazin-2-one;

N-azetidin-3-yl-2-(2-oxo-3,3-diphenylpiperidin-1-yl)acetamide;

1-(2-oxo-2-piperazin-1-ylethyl)-3,3-diphenylpiperidin-2-one;

1-{2-[(1S*,5S*)-3,6-diazabicyclo[3.2.1]oct-3-yl]-2-oxoethyl}-3,3-diphenylpiperidin-2-one;

1-[2-(4-methylpiperazin-1-yl)-2-oxoethyl]-3,3-diphenylpiperidin-2-one; and

3,3-bis(4-fluorophenyl)-1-(2-oxo-2-piperazin-1-ylethyl)piperidin-2-one.

6. A pharmaceutical composition comprising a therapeutically effective amount of a compound of formula (I) according to claim 1 , or a pharmaceutically acceptable salt thereof, in combination with a pharmaceutically acceptable carrier.

7. A method of treating pain in a subject in need thereof, comprising: administering to the subject a therapeutically suitable amount of a compound of formula (I) according to claim 1 , or a pharmaceutically acceptable salt thereof, wherein the pain is selected from the group consisting of acute pain, chronic pain, neuropathic pain, inflammatory pain, visceral pain, cancer pain, allodynia, fibromyalgia, sciatica, back pain, headache pain including migraine, and combinations thereof.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 2, 2013
From: ABBOTT LABORATORIES
To: ABBVIE INC.
Reel/Frame 030137/0198 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 24, 2011
From: DRIZIN, IRENE; DOHERTY, GEORGE; BHATIA, PRAMILA A.; STEWART, ANDREW O.
To: ABBOTT LABORATORIES
Reel/Frame 026333/0031 →