Pharmaceutically active benzsulfonamide derivatives as inhibitors of protein junkinases
View Patent ↗The present invention is related to benzsulfonamide derivatives of formula I notably for use as pharmaceutically active compounds, as well as to pharmaceutical formulations containing such benzsulfonamide derivatives. Said benzsulfonamide derivatives are ef-ficient modulators of the JNK pathway, they are in particular efficient and selective in-hibitors of JNK 2 and 3. The present invention is furthermore related to novel benzsul-fonamide derivatives as well as to methods of their preparation (I). The compounds of formula I according to the present invention being suitable pharma-ceutical agents are those wherein Ar1 is a substituted or unsubstituted aryl or heteroaryl group. X is O or S, preferably O.R1 is hydrogen or a C1-C6-alkyl group, preferably H.R2 is hydrogen, —COOR3, —CONR3R3′, OH, a C1-C4 alkyl substituted with an OH group, a hydrazido carbonyl group, a sulfate, a sulfonate, an amine or an ammonium salt; n is either 0 or 1, preferably 1.
1. A benzsulfonamide according to formula I
with its geometrical isomers, in an optically active form as enantiomers, diastereomers, as well as in the form of racemates, as well as pharmaceutically acceptable salts thereof, wherein
Ar 1 is selected from the group consisting of an unsubstituted aryl group, an unsubstituted heteroaryl group, a substituted aryl group, and a substituted heteroaryl group;
R 1 is hydrogen or a C 1 -C 6 -alkyl group;
R 2 is hydrogen, —COOR 3 , —CONR 3 R 3′ , OH, a C 1 -C 4 alkyl substituted with an OH group, a hydrazido carbonyl group, a sulfate, a sulfonate, an amine or an ammonium salt;
n is either 0 or 1;
Y is a cyclic amine having the formula
whereby, L 1 and L 2 are independently selected from the group consisting of C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 4 -C 8 -cycloalkyl, C 4 -C 8 -cycloalkyl containing 1-3 heteroatoms, C 4 -C 8 -cycloalkyl fused with an aryl, C 4 -C 8 -cycloalkyl fused with a heteroaryl, an unsubstituted aryl group, an unsubstituted heteroaryl group, a substituted aryl group, a substituted heteroaryl group, aryl-C 1 -C 6 -alkyl, heteroaryl- C 1 -C 6 -alkyl, —C(O)—OR 3 , —C(O)—R 3 , —C(O)—NR 3′ R 3 , —NR 3′ R 3 , —NR 3′ C(O)R 3 , —NR 3′ C(O)NR 3′ R 3 , —(SO)R 3 , —(SO 2 )R 3 , —NHSO 2 R 3 , and —SO 2 NR 3′ R 3 ,
with R 3 and R 3′ independently selected from the group consisting of H, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, an unsubstituted aryl group, an unsubstituted heteroaryl group, a substituted aryl group, and a substituted heteroaryl group, aryl-C 1 -C 6 -alkyl, and heteroaryl-C 1 -C 6 -alkyl;
R 6 is selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, OH, halogen, nitro, cyano, sulfonyl, and oxo (═O); and
n′ is an integer from 0 to 4.
2. A benzsulfonamide according to claim 1 , wherein Ar 1 is selected from the group consisting of phenyl, thienyl, furyl, and pyridyl.
3. A benzsulfonamide according to claim 1 , wherein Ar 1 is a phenyl.
4. A benzsulfonamide according to claim 1 , wherein Ar 1 is selected from a halogenophenyl, nitrophenyl, hydroxyphenyl, alkoxy phenyl, pyridyl, 3,4,-dihydroxyphenyl, thioxo-dihydropyridine or its tautomer, pyrazole, R 1 is hydrogen, and n is 1.
5. A benzsulfonamide according to formula I
with its geometrical isomers, in an optically active form as enantiomers, diastereomers, as well as in the form of racemates, as well as pharmaceutically acceptable salts thereof, wherein
Ar 1 is selected from the group consisting of an unsubstituted aryl group, an unsubstituted heteroaryl group, a substituted aryl group, and a substituted heteroaryl group;
R 1 is hydrogen or a C 1 -C 6 -alkyl group;
R 2 is hydrogen, —COOR 3 , —CONR 3 R 3′ , OH, a C 1 -C 4 alkyl substituted with an OH group, a hydrazido carbonyl group, a sulfate, a sulfonate, an amine or an ammonium salt with R 3 and R 3 ′ independently selected from the group consisting of H, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, an unsubstituted aryl group, an unsubstituted heteroaryl group, a substituted aryl group, and a substituted heteroaryl group, and-C 1 -C 6 -alkyl, and heteroaryl-C 1 -C 6 -alkyl;
n is either 0 or 1;
Y is a cyclic amine having the formula
wherein, L 2 is hydrogen, and
L 1 is —NHR 4 ; with R 4 being selected from the group consisting of a straight unsubstituted C 4 -C 12 -alkyl, an unsubstituted branched C 4 -C 12 -alkyl, a straight C 4 -C 12 -alkyl substituted with a cyclohexyl group, a branched C 4 -C 12 -alkyl substituted with a cyclohexyl group, and a benzyl group,
R 6 is hydrogen; and
n′ is an integer from 0 to 4.
6. A benzsulfonamide according to formula I
with its geometrical isomers, in an optically active form as enantiomers, diastereomers, as well as in the form of racemates, as well as pharmaceutically acceptable salts thereof, wherein
Ar 1 is selected from the group consisting of an unsubstituted aryl group, an unsubstituted heteroaryl group, a substituted aryl group, and a substituted heteroaryl group;
R 1 is hydrogen or a C 1 -C 6 -alkyl group;
R 2 is hydrogen, —COOR 3 , —CONR 3 R 3′ , OH, a C 1 -C 4 alkyl substituted with an OH group, a hydrazido carbonyl group, a sulfate, a sulfonate, an amine or an ammonium salt;
n is either 0 or 1;
Y is a piperidine of the following formula
wherein L 1 is —NHR 3 ; with R 3 being selected from the group consisting of a straight unsubstituted C 4 -C 12 -alkyl, an unsubstituted branched C 4 -C 12 -alkyl, a straight C 4 -C 12 -alkyl substituted with a cyclohexyl group, a branched C 4 -C 12 -alkyl substituted with a cyclohexyl group, and a benzyl group,
L 2 is selected from the group consisting of C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 4 -C 8 -cycloalkyl, C 4 -C 8 -cycloalkyl containing 1-3 heteroatoms, C 4 -C 8 -cycloalkyl fused with an aryl, C 4 -C 8 -cycloalkyl fused with a heteroaryl, an unsubstituted aryl group, an unsubstituted heteroaryl group, a substituted aryl group, a substituted heteroaryl group, aryl-C 1 -C 6 -alkyl, heteroaryl- C 1 -C 6 -alkyl, —C(O)—OR 3 , —C(O)—R 3 , —C(O)—NR 3′ R 3 , —NR 3′ R 3, —NR 3′ C(O)R 3 , —NR 3′ C(O)NR 3′ R 3 , —(SO)R 3 , —(SO 2 )R 3 , —NHSO 2 R 3 , and —SO 2 NR 3′ R 3 ,
R 3 ′ is selected from the group consisting of H, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, an unsubstituted aryl group, an unsubstituted heteroaryl group, a substituted aryl group, and a substituted heteroaryl group, aryl-C 1 -C 6 -alkyl, and heteroaryl-C 1 -C 6 -alkyl;
R 6 is selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, OH, halogen, nitro, cyano, sulfonyl, and oxo (═O); and
n′ is an integer from 0 to 4.
7. A benzsulfonamide according to claim 6 , wherein R 3 is a straight or branched C 6 -C 10 -alkyl, optionally substituted with a cyclohexyl group.
8. Sulfonamide compounds (XIX)
wherein
Ar 1 is an aryl or heteroaryl group;
R 1 is hydrogen or a C 1 -C 6 -alkyl group;
R 2 is hydrogen, —COOR 3 , —CONR 3 R 3′ , OH, a C 1 -C 4 alkyl substituted with an OH group, a hydrazido carbonyl group, a sulfate, a sulfonate, an amine or an ammonium salt;
R 3 and R 3′ independently are selected from the group consisting of H, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, an unsubstituted aryl group, an unsubstituted heteroaryl group, a substituted aryl group, and a substituted heteroaryl group, aryl-C 1 -C 6 -alkyl, and heteroaryl-C 1 -C 6 -alkyl;
n is either 0 or 1, and
Y is a piperidine 4-one.
9. A benzsulfonamide selected from the group consisting of
4-chloro-N-(3-{[4-(hexylamino)-1-piperidinyl]sulfonyl}phenyl)benzamide
4-chloro-N-{4-[(4-{[4-(trifluoromethyl)benzyl]amino}-1-piperidinyl)sulfonyl]phenyl}benzamide
4-chloro-N-(4-{[4-({2-[3-(trifluoromethyl)phenyl]ethyl}amino)-1-piperidinyl]sulfonyl}phenyl)benzamide
4-chloro-N-(4-{[4-(hexylamino)-1-piperidinyl]sulfonyl}benzyl)benzamide
4-chloro-N-(4-{[4-(hexylamino)-1-piperidinyl]sulfonyl}phenyl)benzamide
4-chloro-N-(3-{[4-(hexylamino)-1-piperidinyl]sulfonyl}benzyl)benzamide
4-chloro-N-{3-[(4-{[4-(trifluoromethyl)benzyl]amino}-1-piperidinyl)sulfonyl]benzyl}benzamide
4-chloro-N-(3-{[4-({2-[3-(trifluoromethyl)phenyl]ethyl)}amino)-1-piperidinyl]sulfonyl}benzyl)benzamide
4-chloro-N-(4-{[4-({2-[3-(trifluoromethyl)phenyl]ethyl}amino)-1-piperidinyl]sulfonyl}benzyl)benzamide
4-chloro-N-{4-[(4-{[4-(trifluoromethyl)benzyl]amino}-1-piperidinyl)sulfonyl]benzyl}benzamide
4-chloro-N-{3-[(4-{[4-(trifluoromethyl)benzyl]amino}-1-piperidinyl)sulfonyl]phenyl}benzamide
4-chloro-N-{3-[(4-{3-[(trifluoromethyl)sulfonyl]anilino}-1-piperidinyl)sulfonyl]phenyl}benzamide
4-chloro-N-{4-[(4-{3-[(trifluoromethyl)sulfonyl]anilino}-1-piperidinyl)sulfonyl]benzyl}benzamide
N-{3-[(4-anilino-1-piperidinyl)sulfonyl]phenyl}-4-chlorobenzamide
4-chloro-N-(3-{[4-({2-[3-(trifluoromethyl)phenyl]ethyl}amino)-1-piperidinyl]sulfonyl}phenyl)benzamide
4-chloro-N-{3-[(4-{3-[(trifluoromethyl)sulfonyl]anilino}-1-piperidinyl)sulfonyl]benzyl}benzamide
4-chloro-N-{4-[(4-{3-[(trifluoromethyl)sulfonyl]anilino}-1-piperidinyl)sulfonyl]phenyl}benzamide
N-(4-{[4-(hexylamino)-1-piperidinyl]sulfonyl}benzyl)-2-hydroxynicotinamide
N-(3-{[4-(hexylamino)-1-piperidinyl]sulfonyl}benzyl)-2-hydroxynicotinamide
2-hydroxy-N-{3-[(4-{3-[(trifluoromethyl)sulfonyl]anilino}-1-piperidinyl)sulfonyl]benzyl}nicotinamide; and
2-hydroxy-N-{4-[(4-{3-[(trifluoromethyl)sulfonyl]anilino}-1-piperidinyl)sulfonyl]benzyl}nicotinamide.
10. A pharmaceutical composition containing a benzsulfonamide according to claim 1 and a pharmaceutically acceptable carrier, diluent or excipient thereof.
11. Process for the preparation of a benzsulfonamide according to claim 1 , wherein a sulfonamide (XIX)
wherein Ar 1 , R 1 , R 2 and n are as defined in claim 1 and Y is a piperidine 4-one,
is subjected to a reductive amination using an amine H 2 N—R 3 with R 3 as defined in claim 1 .
12. A process according to claim 11 , wherein the following steps are performed:
13. A process according to claim 11 , wherein the following steps are performed: