Amino heterocyclic linked pyrimidine derivatives
View Patent ↗Macrocyclic benzofused pyrimidine compounds, 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.
1. A compound of formula (I):
or a pharmaceutically acceptable salt, wherein:
X is NH, NCH 3 , or O;
Y is N or CR 8 ;
Z is N or CR 9 ;
R 1 is selected from hydrogen, NH 2 , alkyl, or fluoroalkyl;
R 2 , R 3 , R 4 , R 5 , R 6 , and R 7 are each independently selected from the group consisting of hydrogen, alkoxycarbonyl, alkyl, alkylcycloalkyl, carboxy, cyano, cyanoalkyl, cycloalkoxyalkyl, cycloalkyl, fluoroalkoxy, fluoroalkyl, fluorocycloalkyl, fluorocycloalkylalkyl, fluorine, formyl, haloalkoxy, hydroxyalkyl, and C(O)NR 10 R 11 ; or
R 2 and R 3 , or R 4 and R 5 , or R 6 and R 7 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 OCH 2 CH 2 —, —CH 2 OCH 2 CH 2 —, or —OCH 2 CH 2 CH 2 —; or
R 3 and R 4 , or R 5 and R 6 taken together are —CH 2 CH 2 CH 2 —, —CH 2 CH 2 CH 2 CH 2 —, or —CH 2 OCH 2 —;
R 8 and R 9 are each independently selected from the group consisting of hydrogen, fluoroalkyl, and halogen;
R 10 and R 11 are each independently selected from the group consisting of hydrogen and alkyl;
G 1 and G 2 are taken together to form groups of formula (ii) or formula (iv)
L is selected from O, S, NH, or N—CH 3 ;
R 12 and R 13 are each independently selected from the group consisting of hydrogen, alkyl, aryl, and arylalkyl;
R 14 , R 15 , R 16 , and R 17 are each independently selected from the group consisting of hydrogen, acyl, acyloxy, alkenyl, alkoxy, alkoxyalkoxy, alkoxyalkyl, alkoxycarbonyl, alkoxyimino, alkoxysulfonyl, alkyl, alkylcycloalkyl, alkylsulfonyl, alkylthio, alkynyl, amido, aryl, halogen, fluoroalkyl, carboxy, cyano, cyanoalkyl, cycloalkoxyalkyl, cycloalkyl, fluoroalkoxy, fluorocycloalkyl, fluorocycloalkylalkyl, formyl, haloalkoxy, haloalkyl, heteroaryl, heterocycle, hydroxy, hydroxyalkyl, mercapto, nitro, C(O)NR 25 R 26 , NR 25 C(O)alkyl, —NR 26 C(O)Oalkyl, N(R 25 )SO 2 (R 26 ), —NR 25 R 26 , O-aryl, O-heteroaryl, S-aryl, and —SO 2 (NR 25 R 26 ); or
R 15 and R 16 taken together are: —CH 2 CH 2 CH 2 —, —CH 2 CH 2 CH 2 CH 2 —, —CH 2 OCH 2 —, or —OCH 2 CH 2 —;
R 25 and R 26 are independently selected from the group consisting of hydrogen, acyl, alkoxyalkyl, alkyl, aryl, arylalkyl, cyanoalkyl, cycloalkyl, cycloalkoxyalkyl, cycloalkylalkyl, fluoroalkyl, fluorocycloalkylalkyl, and hydroxyalkyl;
m is 0, or 1; and
n is 0, 1, 2, or 3.
2. The compound of claim 1 , wherein G 1 and G 2 taken together are a group of formula (iv)
L is O, S, NH, or N—CH 3 ; and
R 1 is hydrogen or NH 2 .
3. The compound according to claim 2 wherein the compound is N 4 -[2([1]benzofuro[3,2-c]pyrimidin-4-ylamino)ethyl]pyrimidine-2,4-diamine.
4. The compound of claim 1 , wherein G 1 and G 2 taken together are a group of formula
n is 0, 1 or 2; and
R 1 is hydrogen or NH 2 .
5. The compound according to claim 4 wherein the compound is:
N 4 -{2-[(2-aminopyrimidin-4-yl)amino]ethyl}-6,7-dihydro-5H-benzo[6,7]cyclohepta[1,2-d]pyrimidine-2,4-diamine;
N 4 -{2-[(2-aminopyrimidin-4-yl)amino]ethyl}-N 4 -methyl-6,7-dihydro-5H-benzo[6,7]cyclohepta[1,2-d]pyrimidine-2,4-diamine;
N 4 -{3-[(2-aminopyrimidin-4-yl)amino]propyl}-6,7-dihydro-5H-benzo[6,7]cyclohepta[1,2-d]pyrimidine-2,4-diamine; or
N 4 -{2-[(4-aminopyrimidin-2-yl)amino]ethyl}-6,7-dihydro-5H-benzo[6,7]cyclohepta[1,2-d]pyrimidine-2,4-diamine.
6. A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically acceptable carrier.