Quinolone derivative or pharmaceutically acceptable salt thereof
Provided are quinolone derivatives having a lower alkyl or cycloalkyl at the 1-position; —N(R 0 )C(O)-lower alkylene-CO 2 R 0 , lower alkylene-CO 2 R 0 , lower alkenylene-CO 2 R 0 , —O-lower alkylene-CO 2 R 0 , —O-(lower alkylene which may be substituted with —CO 2 R 0 )-aryl or —O-lower alkenylene-CO 2 R 0 (wherein R 0 is H or lower alkyl) at the 3-position; halogen at the 6-position; and amino group substituted with a substituent group having a ring structure at the 7-position, respectively, or pharmaceutically acceptable salts thereof. Pharmaceutical composition containing the quinolone derivatives and methods of using the compositions are provided.
1. A quinolone derivative represented by a formula (I) or a pharmaceutically acceptable salt thereof
wherein
R 1 : a cycloalkyl or lower alkylene-cycloalkyl, wherein the cycloalkyl in R 1 may be substituted;
R 2 : —H or a halogen;
R 3 : —H, a halogen, —OR 0 or —O-lower alkylene-aryl;
R 0 : the same or different from each other and each represents —H or a lower alkyl
R 4 : a lower alkyl, halogeno-lower alkyl, lower alkylene-cycloalkyl, cycloalkyl or heterocyclic group, wherein the cycloalkyl and heterocyclic group in R 4 may respectively be substituted;
R 5 : —NO 2 , —CN, a lower alkyl, lower alkenyl, halogeno lower alkenyl, -L-R a , —C(O)R 0 , —O—R b , —N(R 6 ) 2 , lower alkylene-N(R 6 )(R c ), —N(R 6 )C(O)—R d , lower alkylene-N(R 6 )C(O)—R d , lower) alkylene-N(R 0 )C(O)O-lower alkyl, —N(R 0 )C(O)N(R 0 )—R e , lower alkylene-N(R 0 )C(O)N(R 0 )—R e , —N(R 0 )S(O) 2 N(R 0 )C(O)—R d , —CH═NOH, cycloalkyl, heterocyclic group, (2,4-dioxo-1,3-thiazolidin-5-ylidene)methyl or (4-oxo-2-thioxo-1,3-thiazolidin-5-ylidene)methyl, wherein the cycloalkyl and heterocyclic group in R 5 may respectively be substituted;
R 6 : H, a lower alkyl, lower alkylene-CO 2 R 0 or lower alkylene-P(O)(OR p ) 2 , wherein the lower alkylene in R 6 may be substituted;
L: a lower alkylene or lower alkenylene which may respectively be substituted;
R a : —OR 0 , —CN, —O-lower alkylene-aryl, —O-lower alkylene-CO 2 R 0 , —C(O)R 0 , —CO 2 R 0 , —C(O)NHOH, —C(O)N(R 6 ) 2 , —C(O)N(R 0 )-aryl, —C(O)N(R 0 )—S(O) 2 -lower alkyl, —C(O)N(R 0 )—S(O) 2 -aryl, —C(O)N(R 0 )—S(O) 2 -heterocyclic group, —NH 2 OH, —OC(O)R 0 , —OC(O)-halogeno-lower alkyl, —P(O)(OR p ) 2 , an aryl or heterocyclic group, wherein the aryl and heterocyclic group in R a may be substituted;
R p : R 0 , a lower alkylene-OC(O)-lower alkyl, lower alkylene-OC(O)-cycloalkyl, lower alkylene-OC(O)O-lower alkyl, lower alkylene-OC(O)O-cycloalkyl, or lower alkylene-heterocyclic group, wherein the heterocyclic group in R p may be substituted;
R b : H, a cycloalkyl, aryl, heterocyclic group, lower alkylene-R ba or lower alkenylene-R ba , wherein the lower alkylene, lower alkenylene, cycloalkyl, aryl and heterocyclic group in R b may be substituted;
R ba : —OR 0 , —O—Si(lower alkyl) 3 , —CO 2 R 0 , —C(O)NHOH, —C(O)N(R 0 ) 2 , —C(O)N(R 0 )—S(O) 2 -lower alkyl, —C(O)N(R 0 )—S(O) 2 -aryl, ═C(NH 2 )═NOH, —C(NH 2 )═NO—C(O)R 0 , —C(NH 2 )═NO—C(O)-lower alkylene-C(O)R 0 , —CO 2 -lower alkylene-aryl, —P(O)(OR p ) 2 , —C(O)R 0 , —C(O)-aryl, a cycloalkyl, aryl or heterocyclic group, wherein the aryl and heterocyclic group in R ba may be substituted;
R c : H, a lower alkyl, lower alkylene-OR 0 , lower alkylene-CO 2 R 0 , lower alkylene-C(O)NHOH, lower)alkylene-C(O)N(R 0 ) 2 , lower alkylene-P(O)(OR P ) 2 , lower alkylene-aryl, lower alkylene-heterocyclic group, aryl or heterocyclic group, wherein the lower alkylene, aryl and heterocyclic group in R c may be substituted;
R d : a C 1-7 alkyl, lower alkenyl, halogeno-lower alkyl, lower alkylene-R da , lower alkenylene-R da , cycloalkyl, aryl or heterocyclic group, wherein the lower alkylene, lower alkenylene, cycloalkyl, aryl and heterocyclic group in R d may be substituted;
R da : —CN, —OR 0 , —OC(O)R 0 , —O-lower alkylene-CO 2 R 0 , —O-aryl, —CO 2 R 0 , —C(O)NHOH, —C(O)N(R 0 ) 2 , —CO 2 -lower alkylene-N(R 0 ) 2 , —P(O)(OR P ) 2 , —N(R 6 ) 2 , —N(R 0 )C(O)R 0 , —C(O)N(R 0 )-aryl, —C(O)N(R 0 )-(lower alkylene which may be substituted with —CO 2 R 0 )-aryl, —N(R 0 )C(O)-aryl, —N(R 0 )C(O)—OR 0 , —N(R 0 )C(O)—O-lower alkylene-aryl, —N(R 0 )S(O) 2 -aryl, —S-heterocyclic group, —C(O)N(R 0 )-heterocyclic group, —N(R 0 )C(O)-heterocyclic group, a cycloalkyl, aryl or heterocyclic group, wherein the cycloalkyl, aryl and heterocyclic group in R da may be substituted;
R e : lower alkylene-CO 2 R 0 , lower alkylene-C(O)NHOH, lower)alkylene-C(O)N(R 0 ) 2 , a lower alkylene-heterocyclic group, aryl, heterocyclic group, —S(O) 2 -aryl or —S(O) 2 -heterocyclic group, wherein the aryl and heterocyclic group in R e may be substituted;
X: CH;
A: C(R 7 );
R 7 : —H or a lower alkyl, or R 4 and R 7 may together form a lower alkylene which may be substituted;
with the proviso that 7-(cyclohexylamino)-1-ethyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbonitrile is excluded.
2. The compound according to claim 1 , wherein R 3 is —H, —OH or —F.
3. The compound according to claim 2 , wherein A is CH.
4. The compound according to claim 3 , wherein R 1 is cyclohexyl or cyclopropylmethyl.
5. The compound according to claim 4 , wherein R 2 is —F.
6. The compound according to claim 5 , wherein R 4 is a lower alkyl or cycloalkyl.
7. The compound according to claim 6 , wherein R 5 is —N(R 0 )C(O)-lower alkylene-CO 2 R 0 , lower alkylene-CO 2 R 0 , lower alkenylene-CO 2 R 0 , —O-lower alkylene-CO 2 R 0 , —O-(lower alkylene which may be substituted with —CO 2 R 0 )-aryl or —O-lower alkenylene-CO 2 R 0 .
8. The compound according to claim 1 , which is selected from the group consisting of
4-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]amino}-4-oxobutanoic acid,
5-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]amino}-5-oxopentanoic acid,
(2E)-3-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]acrylic acid,
(2S)-2-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]oxy}-3-phenylpropanoic acid,
(2E)-3-[7-(cyclohexylamino)-6-fluoro-1-isopropyl-4-oxo-1,4-dihydroquinolin-3-yl]acrylic acid,
(2S)-2-{[7-(cyclohexylamino)-6-fluoro-1-isopropyl-4-oxo-1,4-dihydroquinolin-3-yl]oxy}-3-phenylpropanoic acid,
(2S)-2-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]oxy}propanoic acid, and
(2S)-2-{([7-(cyclohexylamino)-6-fluoro-1-isopropyl-4-oxo-1,4-dihydroquinolin-3-yl]oxy}propanoic acid,
or a pharmaceutically acceptable salt thereof.
9. A pharmaceutical composition which comprises the compound or a pharmaceutically acceptable salt thereof according to claim 1 , and a pharmaceutically acceptable carrier.
10. The compound according to claim 1 , wherein A is CH.
11. The compound according to claim 1 , wherein R 1 is cyclohexyl or cyclopropylmethyl.
12. The compound according to claim 11 , wherein R 2 is —F.
13. The compound according to claim 12 , wherein R 4 is a lower alkyl or cycloalkyl.
14. The compound according to claim 13 , wherein R 5 is —N(R 0 )C(O)-lower alkylene-CO 2 R 0 , lower alkylene-CO 2 R 0 , lower alkenylene-CO 2 R 0 , —O-lower alkylene-CO 2 R 0 , —O-(lower alkylene which may be substituted with —CO 2 R 0 )-aryl or —O-lower alkenylene-CO 2 R 0 .
15. A compound of the formula:
or a pharmaceutically acceptable salt thereof.
16. The compound according to claim 15 , which is in a purified form.
17. A pharmaceutical composition comprising the compound or a pharmaceutically acceptable salt thereof according to claim 15 , and a pharmaceutically acceptable carrier.
18. A pharmaceutical composition comprising the compound or a pharmaceutically acceptable salt thereof according to claim 16 , and a pharmaceutically acceptable carrier.