Quinazolinone compounds as anticancer agents
Quinazolinone compounds, pharmaceutically acceptable salts, and prodrugs thereof; compositions that include a pharmaceutically acceptable carrier and one or more of the quinazolinone compounds, either alone or in combination with at least one additional therapeutic agent. Methods of using the quinazolinone compounds, either alone or in combination with at least one additional therapeutic agent, in the prophylaxis or treatment of proliferative diseases.
1. A compound having the formula:
or a stereoisomer, tautomer, or pharmaceutically acceptable salt thereof, wherein
X is O or S;
R 1 is substituted alkyl;
R 2 is selected from the group consisting of
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl, and
(4) substituted or unsubstituted alkynyl;
R 3 is selected from the group consisting of:
(1) CO 2 R 10 , and
(2) CONR 11 R 12 ;
R 4 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl, and
(7) substituted or unsubstituted heterocyclyl;
R 5 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkoxy,
(4) substituted or unsubstituted aryl,
(5) substituted or unsubstituted heteroaryl,
(6) substituted or unsubstituted heterocyclyl,
(7) COR 17 ,
(8) CO 2 R 18 ,
(9) CONR 19 R 20 , and
(10) SO 2 R 21 ;
R 6 , R 7 , R 8 , and R 9 are independently selected from the group consisting of:
(1) hydrogen,
(2) halogen,
(3) hydroxy,
(4) nitro,
(5) amino,
(6) cyano,
(7) alkoxy,
(8) alkylthio,
(9) methylenedioxy,
(10) haloalkoxy,
(11) CO 2 R 10 ,
(12) COR 10 ,
(13) OR 10 ,
(14) CONR 11 R 12 ,
(15) substituted or unsubstituted alkyl,
(16) substituted or unsubstituted aryl,
(17) substituted or unsubstituted heteroaryl,
(18) substituted or unsubstituted alkylamino,
(19) substituted or unsubstituted dialkylamino,
(20) substituted or unsubstituted alkylsulfonyl,
(21) substituted or unsubstituted arylsulfonyl,
(22) substituted or unsubstituted alkylcarboxy,
(23) substituted or unsubstituted carboxamido,
(24) substituted or unsubstituted carboxyamino,
(25) substituted or unsubstituted aminocarboxy,
(26) substituted or unsubstituted aminocarbonyl, and
(27) substituted or unsubstituted alkylsulfonamido;
R 10 , R 11 , R 12 , R 17 , R 18 , R 19 , R 20 , and R 21 are independently selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl, and
(7) substituted or unsubstituted heterocyclyl; or
R 11 and R 12 , or R 19 and R 20 taken together form a 3- to 7-membered carbocyclic or heterocyclic ring; and
m=0, 1, or 2.
2. A compound of claim 1 , wherein R 1 is benzyl.
3. A compound of claim 1 , wherein R 1 is substituted benzyl.
4. A compound of claim 3 , wherein R 1 is a halo-substituted benzyl.
5. A compound of claim 4 , wherein R 1 is 3-chlorobenzyl.
6. A compound of claim 4 , wherein R 1 is 3-fluorobenzyl.
7. A compound of claim 4 , wherein R 1 is 3-methoxybenzyl.
8. A compound of claim 4 , wherein R 1 is 3-trifluoromethylbenzyl.
9. A compound of claim 4 , wherein R 1 is 3-trifluoromethoxybenzyl.
10. A compound of claim 3 , wherein R 1 is 3,5-dimethylbenzyl.
11. A compound of claim 1 , wherein R 1 is 2-naphthylmethyl.
12. A compound having the formula:
or a stereoisomer, tautomer, or pharmaceutically acceptable salt thereof, wherein
X is O or S;
R 1 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl,
(7) substituted or unsubstituted heterocyclyl,
(8) substituted or unsubstituted alkylsulfonyl, and
(9) substituted or unsubstituted arylsulfonyl;
R 2 is hydrogen;
R 3 is CO 2 R 10 ;
R 4 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl, and
(7) substituted or unsubstituted heterocyclyl;
R 5 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkoxy,
(4) substituted or unsubstituted aryl,
(5) substituted or unsubstituted heteroaryl,
(6) substituted or unsubstituted heterocyclyl,
(7) COR 17 ,
(8) CO 2 R 18 ,
(9) CONR 19 R 20 , and
(10) SO 2 R 21 ;
R 6 , R 7 , R 8 , and R 9 are independently selected from the group consisting of:
(1) hydrogen,
(2) halogen,
(3) hydroxy,
(4) nitro,
(5) amino,
(6) cyano,
(7) alkoxy,
(8) alkylthio,
(9) methylenedioxy,
(10) haloalkoxy,
(11) CO 2 R 10 ,
(12) COR 10 ,
(13) OR 10 ,
(14) CONR 11 R 12 ,
(15) substituted or unsubstituted alkyl,
(16) substituted or unsubstituted aryl,
(17) substituted or unsubstituted heteroaryl,
(18) substituted or unsubstituted alkylamino,
(19) substituted or unsubstituted dialkylamino,
(20) substituted or unsubstituted alkylsulfonyl,
(21) substituted or unsubstituted arylsulfonyl,
(22) substituted or unsubstituted alkylcarboxy,
(23) substituted or unsubstituted carboxamido,
(24) substituted or unsubstituted carboxyamino,
(25) substituted or unsubstituted aminocarboxy,
(26) substituted or unsubstituted aminocarbonyl, and
(27) substituted or unsubstituted alkylsulfonamido;
R 10 , R 11 , R 12 , R 17 , R 18 , R 19 , R 20 , and R 21 are independently selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl, and
(7) substituted or unsubstituted heterocyclyl; or
R 11 and R 12 , or R 19 and R 20 taken together form a 3- to 7-membered carbocyclic or heterocyclic ring; and
m=0, 1, or 2.
13. A compound of claim 12 , wherein R 10 is alkyl.
14. A compound of claim 1 , wherein R 2 is hydrogen, R 3 is CONR 11 R 12 , and R 11 and R 12 are alkyl.
15. A compound of claim 14 , wherein R 11 and R 12 are methyl.
16. A compound of claim 1 , wherein R 2 is hydrogen, R 3 is CONR 11 R 12 , and R 11 and R 12 taken together with the nitrogen atom to which they are attached form a 3- to 7-membered heterocyclic ring.
17. A compound having the formula:
or a stereoisomer, tautomer, or pharmaceutically acceptable salt thereof, wherein
X is O or S;
R 1 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl,
(7) substituted or unsubstituted heterocyclyl,
(8) substituted or unsubstituted alkylsulfonyl, and
(9) substituted or unsubstituted arylsulfonyl;
R 2 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl, and
(4) substituted or unsubstituted alkynyl;
R 3 is selected from the group consisting of:
(1) CO 2 R 10 , and
(2) CONR 11 R 12 ;
R 4 is amino-substituted alkyl;
R 5 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkoxy,
(4) substituted or unsubstituted aryl,
(5) substituted or unsubstituted heteroaryl,
(6) substituted or unsubstituted heterocyclyl,
(7) COR 17 ,
(8) CO 2 R 18 ,
(9) CONR 19 R 20 , and
(10) SO 2 R 21 ;
R 6 , R 7 , R 8 , and R 9 are independently selected from the group consisting of:
(1) hydrogen,
(2) halogen,
(3) hydroxy,
(4) nitro,
(5) amino,
(6) cyano,
(7) alkoxy,
(8) alkylthio,
(9) methylenedioxy,
(10) haloalkoxy,
(11) CO 2 R 10 ,
(12) COR 10 ,
(13) OR 10 ,
(14) CONR 11 R 12 ,
(15) substituted or unsubstituted alkyl,
(16) substituted or unsubstituted aryl,
(17) substituted or unsubstituted heteroaryl,
(18) substituted or unsubstituted alkylamino,
(19) substituted or unsubstituted dialkylamino,
(20) substituted or unsubstituted alkylsulfonyl,
(21) substituted or unsubstituted arylsulfonyl,
(22) substituted or unsubstituted alkylcarboxy,
(23) substituted or unsubstituted carboxamido,
(24) substituted or unsubstituted carboxyamino,
(25) substituted or unsubstituted aminocarboxy,
(26) substituted or unsubstituted aminocarbonyl, and
(27) substituted or unsubstituted alkylsulfonamido;
R 10 , R 11 , R 12 , R 17 , R 18 , R 19 , R 20 , and R 21 are independently selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl, and
(7) substituted or unsubstituted heterocyclyl; or
R 11 and R 12 , or R 19 and R 20 taken together form a 3- to 7-membered carbocyclic or heterocyclic ring; and
m=0, 1, or 2.
18. A compound of claim 17 , wherein R 4 is 3-aminopropyl.
19. A compound having the formula:
or a stereoisomer, tautomer, or pharmaceutically acceptable salt thereof, wherein
X is O or S;
R 1 is
substituted alkyl
R 2 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl, and
(4) substituted or unsubstituted alkynyl;
R 3 is selected from the group consisting of:
(1) CO 2 R 10 , and
(2) CONR 11 R 12 ;
R 4 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl, and
(7) substituted or unsubstituted heterocyclyl;
R 5 is hydrogen, alkyl, aryl, or COR 17 ;
R 6 , R 7 , R 8 , and R 9 are independently selected from the group consisting of:
(1) hydrogen,
(2) halogen,
(3) hydroxy,
(4) nitro,
(5) amino,
(6) cyano,
(7) alkoxy,
(8) alkylthio,
(9) methylenedioxy,
(10) haloalkoxy,
(11) CO 2 R 10 ,
(12) COR 10 ,
(13) OR 10 ,
(14) CONR 11 R 12 ,
(15) substituted or unsubstituted alkyl,
(16) substituted or unsubstituted aryl,
(17) substituted or unsubstituted heteroaryl,
(18) substituted or unsubstituted alkylamino,
(19) substituted or unsubstituted dialkylamino,
(20) substituted or unsubstituted alkylsulfonyl,
(21) substituted or unsubstituted arylsulfonyl,
(22) substituted or unsubstituted alkylcarboxy,
(23) substituted or unsubstituted carboxamido,
(24) substituted or unsubstituted carboxyamino,
(25) substituted or unsubstituted aminocarboxy,
(26) substituted or unsubstituted aminocarbonyl, and
(27) substituted or unsubstituted alkylsulfonamido;
R 10 , R 11 , R 12 , R 17 , R 18 , R 19 , R 20 , and R 21 are independently selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl, and
(7) substituted or unsubstituted heterocyclyl; or
R 11 and R 12 , or R 19 and R 20 taken together form a 3- to 7-membered carbocyclic or heterocyclic ring; and
m=0, 1, or 2.
20. A compound of claim 19 , wherein R 5 is COR 17 .
21. A compound of claim 20 , wherein R 17 is aryl, arylalkyl, alkyl-substituted aryl, or halogen-substituted aryl.
22. A compound of claim 21 , wherein aryl is phenyl.
23. A compound having the formula:
or a stereoisomer, tautomer, or pharmaceutically acceptable salt thereof, wherein
X is O or S;
R 1 is
substituted alkyl
R 2 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl, and
(4) substituted or unsubstituted alkynyl;
R 3 is selected from the group consisting of:
(1) CO 2 R 10 , and
(2) CONR 11 R 12 ;
R 4 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl, and
(7) substituted or unsubstituted heterocyclyl;
R 5 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkoxy,
(4) substituted or unsubstituted aryl,
(5) substituted or unsubstituted heteroaryl,
(6) substituted or unsubstituted heterocyclyl,
(7) COR 17 ,
(8) CO 2 R 18 ,
(9) CONR 19 R 20 , and
(10) SO 2 R 21 ;
R 6 , R 8 , and R 9 are independently selected from the group consisting of:
(1) hydrogen,
(2) halogen,
(3) hydroxy,
(4) nitro,
(5) amino,
(6) cyano,
(7) alkoxy,
(8) alkylthio,
(9) methylenedioxy,
(10) haloalkoxy,
(11) CO 2 R 10 ,
(12) COR 10 ,
(13) OR 10 ,
(14) CONR 11 R 12 ,
(15) substituted or unsubstituted alkyl,
(16) substituted or unsubstituted aryl,
(17) substituted or unsubstituted heteroaryl,
(18) substituted or unsubstituted alkylamino,
(19) substituted or unsubstituted dialkylamino,
(20) substituted or unsubstituted alkylsulfonyl,
(21) substituted or unsubstituted arylsulfonyl,
(22) substituted or unsubstituted alkylcarboxy,
(23) substituted or unsubstituted carboxamido,
(24) substituted or unsubstituted carboxyamino,
(25) substituted or unsubstituted aminocarboxy,
(26) substituted or unsubstituted aminocarbonyl, and
(27) substituted or unsubstituted alkylsulfonamido;
R 7 is a halogen;
R 10 , R 11 , R 12 , R 17 , R 18 , R 19 , R 20 , and R 21 are independently selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl, and
(7) substituted or unsubstituted heterocyclyl; or
R 11 and R 12 , or R 19 and R 20 taken together form a 3- to 7-membered carbocyclic or heterocyclic ring; and
m=0, 1, or 2.
24. A compound selected from the group consisting of:
ethyl (3-benzyl-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl){(4-bromobenzoyl)[3-(dimethylamino)propyl]amino}acetate;
ethyl [(3-aminopropyl)(4-methylbenzoyl)amino](3-benzyl-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl)acetate;
isopropyl (3-benzyl-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl)[[3-(dimethylamino)propyl](4-methylbenzoyl)amino]acetate;
isopropyl [(3-aminopropyl)(4-bromobenzoyl)amino](3-benzyl-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl)acetate;
isopropyl [(3-aminopropyl)(4-methylbenzoyl)amino](3-benzyl-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl)acetate;
N-(3-aminopropyl)-N-[1-(3-benzyl-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl)-2-(diethylamino)-2-oxoethyl]-4-bromobenzamide;
N-(3-aminopropyl)-N-[1-(3-benzyl-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl)-2-(diethylamino)-2-oxoethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-(3-benzyl-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl)-2-oxo-2-pyrrolidin-1-ylethyl]-4-bromobenzamide;
N-(3-aminopropyl)-N-[1-(3-benzyl-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl)-2-oxo-2-pyrrolidin-1-ylethyl]-4-chlorobenzamide;
N-(3-aminopropyl)-N-[1-(3-benzyl-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl)-2-morpholin-4-yl-2-oxoethyl]-4-bromobenzamide;
N-(3-aminopropyl)-N-[1-(3-benzyl-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl)-2-morpholin-4-yl-2-oxoethyl]-4-chlorobenzamide;
N-(3-aminopropyl)-N-[1-(3-benzyl-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl)-2-(dimethylamino)-2-oxoethyl]-4-bromobenzamide;
N-(3-aminopropyl)-N-[1-(3-benzyl-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl)-2-(dimethylamino)-2-oxoethyl]-4-chlorobenzamide;
N-(3-aminopropyl)-N-[1-(3-benzyl-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl)-2-oxo-2-pyrrolidin-1-ylethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-(3-benzyl-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl)-2-(dimethylamino)-2-oxoethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-[7-chloro-3-(3-chlorobenzyl)-4-oxo-3,4-dihydroquinazolin-2-yl]-2-(dimethylamino)-2-oxoethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-[7-chloro-3-(3-fluorobenzyl)-4-oxo-3,4-dihydroquinazolin-2-yl]-2-(dimethylamino)-2-oxoethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-[7-chloro-3-(3-methylbenzyl)-4-oxo-3,4-dihydroquinazolin-2-yl]-2-(dimethylamino)-2-oxoethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-{7-chloro-4-oxo-3-[4-(trifluoromethoxy)benzyl]-3,4-dihydroquinazolin-2-yl}-2-(dimethylamino)-2-oxoethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-[7-chloro-3-(4-chlorobenzyl)-4-oxo-3,4-dihydroquinazolin-2-yl]-2-(dimethylamino)-2-oxoethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-[7-chloro-3-(3-methoxybenzyl)-4-oxo-3,4-dihydroquinazolin-2-yl]-2-(dimethylamino)-2-oxoethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-[7-chloro-3-(2-naphthylmethyl)-4-oxo-3,4-dihydroquinazolin-2-yl]-2-(dimethylamino)-2-oxoethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-{7-chloro-4-oxo-3-[3-(trifluoromethyl)benzyl]-3,4-dihydroquinazolin-2-yl}-2-(dimethylamino)-2-oxoethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-{7-chloro-4-oxo-3-[3-(trifluoromethoxy)benzyl]-3,4-dihydroquinazolin-2-yl}-2-(dimethylamino)-2-oxoethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-[7-chloro-3-(3-hydroxybenzyl)-4-oxo-3,4-dihydroquinazolin-2-yl]-2-(dimethylamino)-2-oxoethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-[7-chloro-3-(3,5-dimethylbenzyl)-4-oxo-3,4-dihydroquinazolin-2-yl]-2-(dimethylamino)-2-oxoethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-[3-(1,1′-biphenyl-3-ylmethyl)-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl]-2-(dimethylamino)-2-oxoethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-[7-chloro-3-(3-cyanobenzyl)-4-oxo-3,4-dihydroquinazolin-2-yl]-2-(dimethylamino)-2-oxoethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-[7-chloro-3-(3-nitrobenzyl)-4-oxo-3,4-dihydroquinazolin-2-yl]-2-(dimethylamino)-2-oxoethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-[7-chloro-3-(3,4-dichlorobenzyl)-4-oxo-3,4-dihydroquinazolin-2-yl]-2-(dimethylamino)-2-oxoethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-{1-(3-benzyl-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl)-2-[ethyl(methyl)amino]-2-oxoethyl}-4-methylbenzamide;
N-(3-aminopropyl)-N-{1-[7-chloro-3-(3,5-dimethylbenzyl)-4-oxo-3,4-dihydroquinazolin-2-yl]-2-[ethyl(methyl)amino]-2-oxoethyl}-4-methylbenzamide;
N-(3-aminopropyl)-N-{1-[7-chloro-3-(3,5-dimethylbenzyl)-4-oxo-3,4-dihydroquinazolin-2-yl]-2-[ethyl(methyl)amino]-2-oxoethyl}-4-methylbenzamide;
N-(3-aminopropyl)-N-{1-[7-chloro-3-(3-methoxybenzyl)-4-oxo-3,4-dihydroquinazolin-2-yl]-2-[ethyl(methyl)amino]-2-oxoethyl}-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-[7-chloro-3-(3,5-difluorobenzyl)-4-oxo-3,4-dihydroquinazolin-2-yl]-2-(dimethylamino)-2-oxoethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-{7-chloro-3-[(6-chloropyridin-2-yl)methyl]-4-oxo-3,4-dihydroquinazolin-2-yl}-2-(dimethylamino)-2-oxoethyl]-4-methylbenzamide;
N-(3-aminopropyl)-N-[1-{7-chloro-3-[(2-chloropyridin-4-yl)methyl]-4-oxo-3,4-dihydroquinazolin-2-yl]-2-(dimethylamino)-2-oxoethyl}-4-methylbenzamide; and
N-(3-aminopropyl)-N-[1-[7-chloro-4-oxo-3-(quinolin-2-ylmethyl)-3,4-dihydroquinazolin-2-yl]-2-(dimethylamino)-2-oxoethyl]-4-methylbenzamide.
25. A composition, comprising a pharmaceutically acceptable carrier and an amount of a compound effective to inhibit KSP activity in a human or animal subject when administered thereto, wherein the compound has the formula:
or a stereoisomer, tautomer, or pharmaceutically acceptable salt thereof, wherein
X is O or S;
R 1 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl,
(7) substituted or unsubstituted heterocyclyl,
(8) substituted or unsubstituted alkylsulfonyl, and
(9) substituted or unsubstituted arylsulfonyl;
R 2 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl, and
(4) substituted or unsubstituted alkynyl;
R 3 is selected from the group consisting of:
(1) CO 2 R 10 , and
(2) CONR 11 R 12 ;
with the proviso that when R 4 and R 5 are taken together to form a 5- to 12-membered heterocyclic ring, R 3 is CONR 11 R 12 or R 2 and R 3 taken together with the carbon atom to which they are attached form a 3- to 7-membered carbocyclic or heterocyclic ring;
R 4 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl, and
(7) substituted or unsubstituted heterocyclyl;
R 5 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkoxy,
(4) substituted or unsubstituted aryl,
(5) substituted or unsubstituted heteroaryl,
(6) substituted or unsubstituted heterocyclyl,
(7) COR 17 ,
(8) CO 2 R 18 ,
(9) CONR 19 R 20 , and
(10) SO 2 R 21 ; or
R 4 and R 5 are taken together with the nitrogen atom to which they are attached form a heteroaryl or heterocyclyl ring, wherein the heteroaryl ring contains one or two ring heteroatoms, wherein the heterocyclyl ring contains one or two ring heteroatoms, and wherein the heteroaryl or heterocyclyl ring is optionally substituted with a halogen, alkyl, hydroxy, amino, cyano, alkylamino, dialkylamino, alkylaminoalkyl, dialkylaminoalkyl, alkoxy, aryl, aryloxy, heteroaryl, arylalkyl, heterocycle, aminocarbonyl, carbonylamino, alkylcarbonyl, alkylcarboxy, alkylaminocarbonyl, alkylcarbonylamino, carbocycle, or heteroarylalkyl group; with the proviso that when R 4 and R 5 taken together with the nitrogen atom to which they are attached form a 5-membered heterocyclic ring, the heterocyclic ring is not a 2,4-dioxo-3-oxazolidinyl ring, a 2,5-dioxo-1-imidazolidinyl ring, or a 2,4,5-trioxo-1-imidazolidinyl ring;
R 6 , R 7 , R 8 , and R 9 are independently selected from the group consisting of:
(1) hydrogen,
(2) halogen,
(3) hydroxy,
(4) nitro,
(5) amino,
(6) cyano,
(7) alkoxy,
(8) alkylthio,
(9) methylenedioxy,
(10) haloalkoxy,
(11) CO 2 R 10 ,
(12) COR 10 ,
(13) OR 10 ,
(14) CONR 11 R 12 ,
(15) substituted or unsubstituted alkyl,
(16) substituted or unsubstituted aryl,
(17) substituted or unsubstituted heteroaryl,
(18) substituted or unsubstituted alkylamino,
(19) substituted or unsubstituted dialkylamino,
(20) substituted or unsubstituted alkylsulfonyl,
(21) substituted or unsubstituted arylsulfonyl,
(22) substituted or unsubstituted alkylcarboxy,
(23) substituted or unsubstituted carboxamido,
(24) substituted or unsubstituted carboxyamino,
(25) substituted or unsubstituted aminocarboxy,
(26) substituted or unsubstituted aminocarbonyl, and
(27) substituted or unsubstituted alkylsulfonamido;
R 10 , R 11 , R 12 , R 17 , R 18 , R 19 , R 20 , and R 21 are independently selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl, and
(7) substituted or unsubstituted heterocyclyl; or
R 11 and R 12 , or R 19 and R 20 taken together form a 3- to 7-membered carbocyclic or heterocyclic ring; and
m=0, 1, or 2.
26. The composition of claim 25 further comprising at least one additional agent for the treatment of cancer.
27. The composition of claim 26 , wherein the at least one additional agent for the treatment of cancer is selected from irinotecan, topotecan, gemcitabine, gleevec, herceptin, 5-fluorouracil, leucovorin, carboplatin, cisplatin, taxanes, tezacitabine, cyclophosphamide, vinca alkaloids, imatinib, anthracyclines, rituximab, and trastuzumab.
28. A compound having the formula:
or a stereoisomer, tautomer, or pharmaceutically acceptable salt thereof, wherein
X is O or S;
R 1 is substituted benzyl;
R 2 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl, and
(4) substituted or unsubstituted alkynyl;
R 3 is selected from the group consisting of:
(1) CO 2 R 10 , and
(2) CONR 11 R 12 ;
with the proviso that when R 4 and R 5 are taken together to form a 5- to 12-membered heterocyclic ring, R 3 is CONR 11 R 12 or R 2 and R 3 taken together with the carbon atom to which they are attached form a 3- to 7-membered carbocyclic or heterocyclic ring;
R 4 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl, and
(7) substituted or unsubstituted heterocyclyl;
R 5 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkoxy,
(4) substituted or unsubstituted aryl,
(5) substituted or unsubstituted heteroaryl,
(6) substituted or unsubstituted heterocyclyl,
(7) COR 17 ,
(8) CO 2 R 18 ,
(9) CONR 19 R 20 , and
(10) SO 2 R 21 ; or
R 4 and R 5 are taken together with the nitrogen atom to which they are attached form a heteroaryl or heterocyclyl ring, wherein the heteroaryl ring contains one or two ring heteroatoms, wherein the heterocyclyl ring contains one or two ring heteroatoms, and wherein the heteroaryl or heterocyclyl ring is optionally substituted with a halogen, alkyl, hydroxy, amino, cyano, alkylamino, dialkylamino, alkylaminoalkyl, dialkylaminoalkyl, alkoxy, aryl, aryloxy, heteroaryl, arylalkyl, heterocycle, aminocarbonyl, carbonylamino, alkylcarbonyl, alkylcarboxy, alkylaminocarbonyl, alkylcarbonylamino, carbocycle, or heteroarylalkyl group; with the proviso that when R 4 and R 5 taken together with the nitrogen atom to which they are attached form a 5-membered heterocyclic ring, the heterocyclic ring is not a 2,4-dioxo-3-oxazolidinyl ring, a 2,5-dioxo-1-imidazolidinyl ring, or a 2,4,5-trioxo-1-imidazolidinyl ring;
R 6 , R 7 , R 8 , and R 9 are independently selected from the group consisting of:
(1) hydrogen,
(2) halogen,
(3) hydroxy,
(4) nitro,
(5) amino,
(6) cyano,
(7) alkoxy,
(8) alkylthio,
(9) methylenedioxy,
(10) haloalkoxy,
(11) CO 2 R 10 ,
(12) COR 10 ,
(13) OR 10 ,
(14) CONR 11 R 12 ,
(15) substituted or unsubstituted alkyl,
(16) substituted or unsubstituted aryl,
(17) substituted or unsubstituted heteroaryl,
(18) substituted or unsubstituted alkylamino,
(19) substituted or unsubstituted dialkylamino,
(20) substituted or unsubstituted alkylsulfonyl,
(21) substituted or unsubstituted arylsulfonyl,
(22) substituted or unsubstituted alkylcarboxy,
(23) substituted or unsubstituted carboxamido,
(24) substituted or unsubstituted carboxyamino,
(25) substituted or unsubstituted aminocarboxy,
(26) substituted or unsubstituted aminocarbonyl, and
(27) substituted or unsubstituted alkylsulfonamido;
R 10 , R 11 , R 12 , R 17 , R 18 , R 19 , R 20 , and R 21 are independently selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl, and
(7) substituted or unsubstituted heterocyclyl; or
R 11 and R 12 , or R 19 and R 20 taken together form a 3- to 7-membered carbocyclic or heterocyclic ring; and
m=0, 1, or 2.
29. A compound having the formula:
or a stereoisomer, tautomer, or pharmaceutically acceptable salt thereof, wherein
X is O or S;
R 1 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl,
(7) substituted or unsubstituted heterocyclyl,
(8) substituted or unsubstituted alkylsulfonyl, and
(9) substituted or unsubstituted arylsulfonyl;
R 2 is hydrogen;
R 3 is CO 2 R 10 ;
R 4 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl, and
(7) substituted or unsubstituted heterocyclyl;
R 5 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkoxy,
(4) substituted or unsubstituted aryl,
(5) substituted or unsubstituted heteroaryl,
(6) substituted or unsubstituted heterocyclyl,
(7) COR 17 ,
(8) CO 2 R 18 ,
(9) CONR 19 R 20 , and
(10) SO 2 R 21 ; or
R 4 and R 5 are taken together with the nitrogen atom to which they are attached form a heteroaryl or heterocyclyl ring, wherein the heteroaryl ring contains one or two ring heteroatoms, wherein the heterocyclyl ring contains one or two ring heteroatoms, and wherein the heteroaryl or heterocyclyl ring is optionally substituted with a halogen, alkyl, hydroxy, amino, cyano, alkylamino, dialkylamino, alkylaminoalkyl, dialkylaminoalkyl, alkoxy, aryl, aryloxy, heteroaryl, arylalkyl, heterocycle, aminocarbonyl, carbonylamino, alkylcarbonyl, alkylcarboxy, alkylaminocarbonyl, alkylcarbonylamino, carbocycle, or heteroarylalkyl group; with the proviso that when R 4 and R 5 taken together with the nitrogen atom to which they are attached form a 5-membered heterocyclic ring, the heterocyclic ring is not a 2,4-dioxo-3-oxazolidinyl ring, a 2,5-dioxo-1-imidazolidinyl ring, or a 2,4,5-trioxo-1-imidazolidinyl ring;
R 6 , R 7 , R 8 , and R 9 are independently selected from the group consisting of:
(1) hydrogen,
(2) halogen,
(3) hydroxy,
(4) nitro,
(5) amino,
(6) cyano,
(7) alkoxy,
(8) alkylthio,
(9) methylenedioxy,
(10) haloalkoxy,
(11) CO 2 R 10 ,
(12) COR 10 ,
(13) OR 10 ,
(14) CONR 11 R 12 ,
(15) substituted or unsubstituted alkyl,
(16) substituted or unsubstituted aryl,
(17) substituted or unsubstituted heteroaryl,
(18) substituted or unsubstituted alkylamino,
(19) substituted or unsubstituted dialkylamino,
(20) substituted or unsubstituted alkylsulfonyl,
(21) substituted or unsubstituted arylsulfonyl,
(22) substituted or unsubstituted alkylcarboxy,
(23) substituted or unsubstituted carboxamido,
(24) substituted or unsubstituted carboxyamino,
(25) substituted or unsubstituted aminocarboxy,
(26) substituted or unsubstituted aminocarbonyl, and
(27) substituted or unsubstituted alkylsulfonamido;
R 10 , R 11 , R 12 , R 17 , R 18 , R 19 , R 20 , and R 21 are independently selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl, and
(7) substituted or unsubstituted heterocyclyl; or
R 11 and R 12 , or R 19 and R 20 taken together form a 3- to 7-membered carbocyclic or heterocyclic ring; and
m=0, 1, or 2.
30. A compound having the formula:
or a stereoisomer, tautomer, or pharmaceutically acceptable salt thereof, wherein
X is O or S;
R 1 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyi,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl,
(7) substituted or unsubstituted heterocyclyl,
(8) substituted or unsubstituted alkylsulfonyl, and
(9) substituted or unsubstituted arylsulfonyl;
R 2 is hydrogen;
R 3 is CONR 11 R 12 , wherein R 11 and R 12 are alkyl;
R 4 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl, and
(7) substituted or unsubstituted heterocyclyl;
R 5 is selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkoxy,
(4) substituted or unsubstituted aryl,
(5) substituted or unsubstituted heteroaryl,
(6) substituted or unsubstituted heterocyclyl,
(7) COR 17 ,
(8) CO 2 R 18 ,
(9) CONR 19 R 20 , and
(10) SO 2 R 21 ; or
R 4 and R 5 are taken together with the nitrogen atom to which they are attached form a heteroaryl or heterocyclyl ring, wherein the heteroaryl ring contains one or two ring heteroatoms, wherein the heterocyclyl ring contains one or two ring heteroatoms, and wherein the heteroaryl or heterocyclyl ring is optionally substituted with a halogen, alkyl, hydroxy, amino, cyano, alkylamino, dialkylamino, alkylaminoalkyl, dialkylaminoalkyl, alkoxy, aryl, aryloxy, heteroaryl, arylalkyl, heterocycle, aminocarbonyl, carbonylamino, alkylcarbonyl, alkylcarboxy, alkylaminocarbonyl, alkylcarbonylamino, carbocycle, or heteroarylalkyl group; with the proviso that when R 4 and R 5 taken together with the nitrogen atom to which they are attached form a 5-membered heterocyclic ring, the heterocyclic ring is not a 2,4-dioxo-3-oxazolidinyl ring, a 2,5-dioxo-1-imidazolidinyl ring, or a 2,4,5-trioxo-1-imidazolidinyl ring;
R 6 , R 7 , R 8 , and R 9 are independently selected from the group consisting of:
(1) hydrogen,
(2) halogen,
(3) hydroxy,
(4) nitro,
(5) amino,
(6) cyano,
(7) alkoxy,
(8) alkylthio,
(9) methylenedioxy,
(10) haloalkoxy,
(11) CO 2 R 10 ,
(12) COR 10 ,
(13) OR 10 ,
(14) CONR 11 R 12 ,
(15) substituted or unsubstituted alkyl,
(16) substituted or unsubstituted aryl,
(17) substituted or unsubstituted heteroaryl,
(18) substituted or unsubstituted alkylamino,
(19) substituted or unsubstituted dialkylamino,
(20) substituted or unsubstituted alkylsulfonyl,
(21) substituted or unsubstituted arylsulfonyl,
(22) substituted or unsubstituted alkylcarboxy,
(23) substituted or unsubstituted carboxamido,
(24) substituted or unsubstituted carboxyamino,
(25) substituted or unsubstituted aminocarboxy,
(26) substituted or unsubstituted aminocarbonyl, and
(27) substituted or unsubstituted alkylsulfonamido;
R 10 , R 17 , R 18 , R 19 , R 20 , and R 21 are independently selected from the group consisting of:
(1) hydrogen,
(2) substituted or unsubstituted alkyl,
(3) substituted or unsubstituted alkenyl,
(4) substituted or unsubstituted alkynyl,
(5) substituted or unsubstituted aryl,
(6) substituted or unsubstituted heteroaryl, and
(7) substituted or unsubstituted heterocyclyl; or
R 19 and R 20 taken together form a 3- to 7-membered carbocyclic or heterocyclic ring; and
m=0, 1, or 2.