Arylpiperidinol and arylpiperidine derivatives and pharmaceuticals containing the same
View Patent ↗A pharmaceutical composition, especially a pharmaceutical composition for the alleviation or treatment of symptoms due to ischemic diseases and symptoms derived from seizures, epilepsy, and migraine, and a Ca 2+ overload suppressant, containing an arylpiperidinol or arylpiperidine derivative having the formula (I): wherein, R is H, an optionally substituted phenyl, an optionally substituted phenoxy, or an optionally substituted benzoyl, A is a connecting bond, a cycloalkylene, or an alkenylene optionally substituted with a lower alkyl, B is an alkylene optionally substituted with OH or an alkoxy or —NHCO(CH 2 ) n — where n is an integer of 1 to 5, E is a connecting bond, O, or a methylene, X is OH or H provided that when E is O or a methylene, X is not H, and Y and Z are independently H, a halogen, an alkoxy, or an alkyl optionally substituted with a halogen.
1. A compound having the formula (I′):
wherein,
R′ is a phenyl group optionally substituted with a substituent selected from the group consisting of a halogen atom, a hydroxyl group, a C1-C5 optionally branched alkoxy group, and a C1-C5 optionally branched alkyl group optionally substituted with a halogen atom; a phenoxy group optionally substituted with a substituent selected from the group consisting of a halogen atom, a hydroxyl group, a C1-C5 optionally branched alkoxy group, and a C1-C5 optionally branched alkyl group optionally substituted with a halogen atom; or a benzoyl group optionally substituted with a substituent selected from the group consisting of a halogen atom, a hydroxyl group, a C1-C5 optionally branched alkoxy group, a C1-C5 optionally branched alkyl group optionally substituted with a halogen atom,
A is a connecting bond,
B is an alkylene group optionally substituted with a hydroxyl group or an alkoxy group,
E is an oxygen atom,
X is a hydroxyl group, and
Y and Z may be the same or different from each other and represent a hydrogen atom, a halogen atom, an alkoxy group, or an alkyl group optionally substituted with a halogen atom,
provided that, when R′ is a phenyl group optionally substituted with a substituent selected from the group consisting of a halogen atom, a hydroxyl group, a C1-C5 optionally branched alkoxy group, and a C1-C5 optionally branched alkyl group optionally substituted with a halogen atom, B is not an unsubstituted alkylene group, and that when R′ is a phenoxy group optionally substituted with a substituent selected from the group consisting of a halogen atom, a hydroxyl group, a C1-C5 optionally branched alkoxy group, and a C1-C5 optionally branched alkyl group optionally substituted with a halogen atom, B is not an unsubstituted alkylene group,
or its pharmaceutically acceptable salt.
2. A compound or its pharmaceutically acceptable salt as claimed in claim 1 , wherein, in the formula (I′), R′, A, B, and X are selected from the group consisting of:
1) R′ is a phenyl group optionally substituted with a substituent selected from the group consisting of a halogen atom, a hydroxyl group, a C1-C5 optionally branched alkoxy group, and a C1-C5 optionally branched alkyl group optionally substituted with a halogen atom, A is a connecting bond, B is an alkylene group substituted with a hydroxyl group, and X is a hydroxyl group;
2) R′ is a phenoxy group optionally substituted with a substituent selected from the group consisting of a halogen atom, a hydroxyl group, a C1-C5 optionally branched alkoxy group, and a C1-C5 optionally branched alkyl group optionally substituted with a halogen atom, A is a connecting bond, B is an alkylene group substituted with a hydroxyl group, and X is a hydroxyl group; and
3) R′ is a benzoyl group optionally substituted with a substituent selected from the group consisting of a halogen atom, a hydroxyl group, a C1-C5 optionally branched alkoxy group, a C1-C5 optionally branched alkyl group optionally substituted with a halogen atom, A is a connecting bond, B is an alkylene group optionally substituted with a hydroxyl group or an alkoxy group and X is a hydroxyl group where further E is an oxygen atom, Y and Z may be the same or different from each other and represent a hydrogen atom, a halogen atom, an alkoxy group, or an alkyl group optionally substituted with a halogen atom.
3. A compound or its pharmaceutically acceptable salt as claimed in claim 1 or claim 2 , wherein, in the formula (I′), R′ is a benzoyl group optionally substituted with a substituent selected from the group consisting of a halogen atom, a hydroxyl group, a C1-C5 optionally branched alkoxy group, a C1-C5 optionally branched alkyl group optionally substituted with a halogen atom, A is a connecting bond, and X is a hydroxyl group.
4. A compound or its pharmaceutically acceptable salt as claimed in claim 1 or claim 2 , wherein, in the formula (I′), R′ is a phenyl group optionally substituted with a substituent selected from the group consisting of a halogen atom, a hydroxyl group, a C1-C5 optionally branched alkoxy group, and a C1-C5 optionally branched alkyl group optionally substituted with a halogen atom, A is a connecting bond, B is a dimethylene group substituted with a hydroxyl group, and X is a hydroxyl group.
5. A compound or its pharmaceutically acceptable salt as claimed in claim 1 or claim 2 , wherein, in the formula (I′), R′ is a phenoxy group optionally substituted with a substituent selected from the group consisting of a halogen atom, a hydroxyl group, a C1-C5 optionally branched alkoxy group, and a C1-C5 optionally branched alkyl group optionally substituted with a halogen atom, A is a connecting bond, B is a trimethylene group substituted with a hydroxyl group, and X is a hydroxyl group.
6. A pharmaceutical composition containing the compound having the formula (I′) according to claim 1 or its pharmaceutically acceptable salt and a pharmaceutical acceptable carrier.