IP Library Granted Patent US 8,278,313
Granted Patent B2
US 8,278,313 · App. 12/401,385 · Granted Oct 2, 2012

Macrocyclic spiro pyrimidine derivatives

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Quick Facts
Patent No.
US 8,278,313
App. No.
12/401,385
Granted
Oct 2, 2012
Kind
B2
Abstract

Macrocyclic Spiro pyrimidine compounds of formula (I): compositions comprising such compounds, methods for making the compounds, and methods of treating and preventing the progression of diseases, conditions, and disorders using such compounds and compositions are described herein.

Claims (19)

1. A compound of formula (I):

or a pharmaceutically acceptable salt thereof, wherein:

G 1 is CH 2 CH 2 ;

G 2 is CH 2 ;

wherein each carbon of G 1 and G 2 may be optionally substituted with one or more groups selected from acyl, acyloxy, alkenyl, alkoxy, alkoxyalkyl, alkoxyalkoxy, alkoxycarbonyl, alkyl, alkylcarbonyl, alkylcycloalkyl, alkylsulfonyl, alkylthio, alkynyl, amido, carboxy, cyano, cyanoalkyl, cycloalkoxyalkyl, cycloalkyl, fluoroalkoxy, fluoroalkyl, fluorocycloalkyl, fluorocycloalkylalkyl, formyl, haloalkoxy, haloalkyl, halogen, hydroxy, hydroxyalkyl, mercapto, nitro, and oxo;

G 4 is a bond;

R 1 is selected from hydrogen, NH 2 , —NH(acyl), —NH(alkyl), —N(alkyl) 2 , —NH(C═O)aryl, —NH-alkylene(NR 8 R 9 ), —NH(C═O)-alkylene(NR 8 R 9 ), —NR 8 (C═O)NR 8 R 9 , —NH-alkylene-heteroaryl, —NHOH, —NHOCH 3 , —O-alkylene(NR 8 R 9 ), alkoxy, alkoxycarbonyl, alkyl, carboxy, —(C═O)—(NR 8 R 9 ), —(C═O)—NH-alkylene(NR 8 R 9 ), cyano, cyanoalkyl, cycloalkyl, fluoroalkyl, fluorocycloalkyl, hydroxyalkyl, and piperazinyl;

R 8 and R 9 each are each independently selected from acyl, alkoxyalkyl, alkoxycarbonyl, alkyl, alkylcarbonyl, alkylcycloalkyl, alkylsulfonyl, amido, aryl, cyanoalkyl, cycloalkoxyalkyl, cycloalkyl, fluorocycloalkyl, fluorocycloalkylalkyl, heteroaryl, heterocyclyl, hydrogen, formyl, hydroxy, and hydroxyalkyl;

R 10 and R 11 taken together are alkylene, —OCH 2 CH 2 O—, —OCH 2 CH 2 CH 2 O—, or —CH 2 CH 2 OCH 2 CH 2 —,

A 1 is

 and

wherein each carbon atom of groups A 1 may be optionally substituted with one or more groups selected from acyl, acyloxy, alkenyl, alkoxy, alkoxyalkoxy, alkoxyalkyl, alkoxycarbonyl, alkyl, alkylcarbonyl, alkylcycloalkyl, alkylsulfonyl, alkylthio, alkynyl, amido, carboxy, cyano, cyanoalkyl, cycloalkoxyalkyl, cycloalkyl, fluoroalkoxy, fluoroalkyl, fluorocycloalkyl, fluorocycloalkylalkyl, formyl, haloalkoxy, haloalkyl, halogen, hydroxy, hydroxyalkyl, mercapto, and nitro.

2. The compound of claim 1 , wherein R 1 is selected from hydrogen, NHOH, —NHOCH 3 , alkoxy, cyano, cyanoalkyl, cycloalkyl, fluoroalkyl, fluorocycloalkyl, and hydroxyalkyl.

3. The compound of claim 1 , wherein R 1 is hydrogen, NH 2 , —NHCH 3 , —NH(C═O)CH 3 , —NH(C═O)phenyl, —NH(C═O)NHCH 3 , —NH(C═O)CH 2 NH 2 , —NH(C═O)CH 2 NHCH 3 , —NH(C═O)CH 2 N(CH 3 ) 2 , —NH(C═O)CH 2 CH 2 CH 2 NH 2 , —NHCH 2 (pyridin-3-yl), —NHCH 2 (imidazol-4-yl), —NHCH 2 CH 2 N(CH 3 ) 2 , piperazin-1-yl, —(C═O)OCH 3 , or —(C═O)OH.

4. The compound of claim 1 , wherein R 10 and R 11 taken together are —CH 2 CH 2 —, —CH 2 CH 2 CH 2 —, —CH 2 CH 2 CH 2 CH 2 —, —CH 2 CH 2 CH 2 CH 2 CH 2 —, —CH 2 CH 2 CH 2 CH 2 CH 2 CH 2 —, —OCH 2 CH 2 O—, —OCH 2 CH 2 CH 2 O—, or —CH 2 CH 2 OCH 2 CH 2 .

5. The compound of claim 1 , wherein the compound is selected form the group consisting of:

4′-(3-(methylamino)azetidin-1-yl)-6′,7′-dihydro-5′H-spiro[cyclopentane-1,8′-quinazolin ]-2′-amine; and

4′-(3-aminoazetidin-1-yl)-6′,7′-dihydro-5′H-spiro[cyclopentane-1,8′-quinazolin]-2′-amine.

6. A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically acceptable carrier.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 17, 2013
From: ABBOTT LABORATORIES
To: ABBVIE INC.
Reel/Frame 030237/0588 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 28, 2010
From: LIU, HUAQING; KOENIG, JOHN R.; COWART, MARLON D.; BLACK, LAWRENCE A.
To: ABBOTT LABORATORIES
Reel/Frame 024458/0351 →