Spirocyclic derivatives as histone deacetylase inhibitors
This invention is related to new histone deacetylase inhibitors according to the general formula (I) wherein: the dotted line is an optional additional bond; n is zero or an integer from 1 to 4; R 1 is hydrogen; C 1 -C 6 alkyl, optionally substituted by cycloalkyl, aryl or by heteroaryl; (CO)R 3 ; (SO 2 )R 4 ; cycloalkyl; aryl; or heteroaryl; R 2 is C 1 -C 6 alkyl, optionally substituted by aryl or by heteroaryl; aryl; heteroaryl; or (CO)R 5 ; X is CH 2 , oxygen or NR 6 ; Y is a bond, CHR 7 or NR 8 ; Z is oxygen, CR 9 R 10 or C═R 11 ; and R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 and R 11 are as further defined in the specification; and pharmaceutical acceptable salts thereof.
1. Process to prepare the compounds of formula (I)
and pharmaceutically acceptable salts thereof, wherein:
the dotted line is an optional additional bond;
n is zero or 1;
R 1 is hydrogen; C 1 -C 4 alkyl; C 1 -C 4 alkyl substituted by phenyl or phenyl substituted by halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, amino, C 1 -C 4 alkylamino or phenyl; C 1 -C 4 alkyl substituted by 2-phenyl-thiazolyl, pyridyl, indolyl, quinolyl, or indolyl substituted by halogen or C 1 -C 4 alkyl; (CO)R 3 ; (SO 2 )R 4 ; cyclopentyl; phenyl; or pyrimidinyl;
R 2 is phenyl or (CO)NH-phenyl;
X is oxygen or NH;
Y is a bond; CHR′; NH; N—C 1 -C 4 alkyl; or N—C 1 -C 4 alkyl substituted by phenyl;
Z is CR 9 R 10 ; C═O; C═NOH; C═NO—C 1 -C 4 alkyl; or C═NO—C 1 -C 4 alkyl substituted by phenyl;
R 3 is C 1 -C 4 alkyl; phenyl; O—C 1 -C 4 alkyl; NH—C 1 -C 4 alkyl; NH—C 1 -C 4 alkyl substituted by phenyl; or NH-phenyl;
R 4 is C 1 -C 4 or phenyl;
R 7 is hydrogen; or is absent, when said additional bond is present;
R 9 is hydrogen; or is absent, when said additional bond is present;
R 10 is hydrogen; hydroxyl; or C 1 -C 4 acylamino;
provided that when said additional bond is present, then Y and Z are CH;
said process comprising either:
a′) treating a compound of formula:
with a compound of formula HNOR 16 , where R 16 is H, C 1 -C 4 alkyl, or C 1 -C 4 alkyl substituted by phenyl, thus obtaining the compounds of formula (I) where Z is C═NOR 16 ; or
a″) treating a compound of formula:
wherein Z is CR 9 R 10 or C═O,
with a protected hydroxylamine, followed by a deprotection reaction, thus obtaining the compounds of formula (I) where Z is CR 9 R 10 or C═O.
2. Process according to claim 1 , wherein in the case a′), the reaction is conducted in a suitable solvent in presence of a base.
3. Process according to claim 2 , wherein the solvent is ethanol or dimethylformamide, and the base is pyridine.
4. Process according to claim 1 , wherein in the case a″), the reaction with the protected hydroxylamine is conducted in a suitable solvent in presence of a condensating agent and optionally a base.
5. Process according to claim 4 , wherein the solvent is tetrahydrofuran, dichloromethane or dimethylformamide, the condensating agent is 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide, and the optional base is triethylamine or diisopropylethylamine.
6. A method of treating colon cancer in a subject in need thereof, comprising administering a compound of formula (I) prepared according to the process of claim 1 to said subject in an amount effective to treat said colon cancer.
7. A method of treating myelogenous leukemia in a subject in need thereof, comprising administering a compound of formula (I) prepared according to the process of claim 1 to said subject in an amount effective to treat said myelogenous leukemia.
8. A method of treating basal cell carcinoma in a subject in need thereof, comprising administering a compound of formula (I) prepared according to the process of claim 1 to said subject in an amount effective to treat said basal cell carcinoma.