Treatment of oppositional defiant disorder and conduct disorder with 5-aminoalkyl-4,5,6,7-tetrahydro-4-oxyindolones
View Patent ↗A method for treating the psychiatric disorders known as oppositional defiant disorder and conduct disorder is disclosed. The method comprises the administration of a compound according to Formula I or II to a patient suffering from oppositional defiant disorder and/or conduct disorder. The compound may be either a racemic mixture or e.g. the levorotatory form. It may be short acting or in a sustained release, long acting form. Molindone or a pharmaceutically acceptable salt of molindone is a preferred embodiment.
1. A method of treating oppositional defiant disorder in a patient diagnosed therewith wherein said method comprises administering a therapeutically effective amount of indole compound I, represented by general formula I,
or the indole compound I as a pharmaceutically acceptable acid addition salt of the compound of general formula I to said patient,
wherein:
n is 2 or 3;
R 1 designates hydrogen, a lower alkyl, benzyl, phenyl or 2-, 3- or 4-pyridyl;
R 2 and R 3 are each independently alkyl, alkenyl, cycloalkyl, phenyl, halogeno-phenyl or lower alkoxy phenyl;
R 4 designates hydrogen or a lower alkyl and is attached to carbon atom 6 or 7 of the indole nucleus; and
X and Y designate lower alkyl, hydroxy lower alkyl, lower acyloxy alkyl, carbamoyloxy lower alkyl and phenyl lower alkyl or alternatively X and Y may be linked together and then constitute, together with the nitrogen atom to which they are attached, an NXY moiety that is an optionally substituted heterocyclic ring.
2. A method of treating oppositional defiant disorder in a patient diagnosed therewith wherein said method comprises administering a therapeutically effective amount of indole compound II, represented by general formula II,
or the indole compound II as a pharmaceutically acceptable acid addition salt of the compound of general formula II, to said patient,
wherein:
n is 2 or 3;
R 1 , R 2 , R 3 and R 4 are each independently a hydrogen atom, an optionally substituted alkyl, an optionally substituted alkenyl or an optionally substituted alkynyl radical (the optional substituent of the alkyl, alkenyl or alkynyl radical being 1-3 radicals of amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino or alkylsulfonylamino); a hydroxy group, an alkoxy group, an alkylthio group, an alkylsulfinyl group, a lower alkylsulfonyl group, a halogen atom, a carboxyl group, a lower alkoxy-carbonyl group, a benzyloxycarbonyl group, a cyano group, a benzyloxy group, a lower alkanoyloxy group, a cycloalkyl group, a cycloalkyl group, an aryl group, an aralkyl group, a substituted aryl group, a heteroaryl group, a substituted heteroaryl group, a benzenesulfonyloxy group being optionally substituted by an alkyl group; a lower alkanoylamino group, a lower alkoxycarbonylamino group, a lower alkylsulfonamido group or a phthalimido group;
or R 3 is also one or more members selected from the group consisting of hydrogen, amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino, and alkylsulfonylamido;
X and Y designate lower alkyl, hydroxy lower alkyl, lower acyloxy alkyl, carbamoyloxy lower alkyl and phenyl lower alkyl, or X and Y may be linked together and then constitute, together with the nitrogen atom to which they are attached, an NXY moiety that is an optionally substituted heterocyclic ring; and
Z is selected from the group consisting of oxo, thio, seleno, telluro, and NH.
3. The method of claim 1 wherein said n is 2 and said NXY moiety is morpholine.
4. The method of claim 1 , wherein said n is 2 and said NXY moiety is N-(2-methyoxyphenyl)piperazine.
5. The method of claim 1 or 2 , wherein said indole compound is to be administered orally.
6. The method of claim 1 or 2 , wherein said indole compound is to be administered intramuscularly.
7. The method of claim 1 or 2 , wherein said indole compound is to be administered 2, 3, 4 or 5 times a day.
8. The method of claim 1 or 2 , wherein said indole compound is to be administered at a dose of from 1-20 mg every 4 hours.
9. The method of claim 1 or 2 , wherein said indole compound is to be administered at a dose of 10 mg twice per day.
10. The method of claim 1 or 2 , wherein said compound of formula I or II or pharmaceutically acceptable acid addition salt thereof is to be administered in a long lasting formulation.
11. The method of claim 10 , wherein said compound of formula I or II or pharmaceutically acceptable acid addition salt of thereof is to be administered once daily.
12. The method of claim 10 , wherein said compound of formula I or II or pharmaceutically acceptable acid addition salt thereof is to be administered at least once per week but less than once per day.
13. The method of claim 1 or 2 , wherein said compound of formula I or II or pharmaceutically acceptable acid addition salt thereof is to be administered in the form of a patch.
14. The method of claim 1 or 2 , wherein said compound of formula I or II or pharmaceutically acceptable acid addition salt thereof comprises the levorotatory enantiomer thereof in the absence of any substantial amount of the dextrorotatory enantiomer.
15. The method of claim 1 or 2 , wherein said compound of formula I or II or pharmaceutically acceptable acid addition salt thereof is to be administered with another drug.
16. The method of claim 15 , wherein said another drug is lithium.
17. A method of treating oppositional defiant disorder in a patient diagnosed therewith, wherein said method comprises administering a dihydroindoline analogue of compound I or II or a pharmaceutically acceptable acid salt of said analogue to said patient, wherein said compound I is represented by the general formula I,
wherein:
n is 2 or 3;
R 1 designates hydrogen, a lower alkyl, benzyl, phenyl or 2-, 3- or 4-pyridyl;
R 2 and R 3 are each independently alkyl, alkenyl and cycloalkyl, phenyl, halogeno-phenyl or lower alkoxy phenyl;
R 4 designates hydrogen or a lower alkyl and being attached to carbon atom 6 or 7 of the indole nucleus; and
X and Y designate lower alkyl, hydroxy lower alkyl, lower acyloxy alkyl, carbamoyloxy lower alkyl and phenyl lower alkyl or alternatively X and Y may be linked together and then constitute, together with the nitrogen atom to which they are attached, an NXY moiety that is an optionally substituted heterocyclic ring;
and wherein said compound II is represented by general formula II,
wherein:
n is 2 or 3;
R 1 , R 2 , R 3 and R 4 are each independently a hydrogen, alkyl, a alkenyl or a alkynyl radical optionally substituted by 1-3 radicals of amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino, alkylsulfonylamino, a hydrogen atom, hydroxy, alkoxy, alkylthio, an alkylsulfinyl group, a lower alkylsulfonyl group, halo, a carboxyl group, a lower alkoxy-carbonyl group, a benzyloxycarbonyl group, a cyano group, a benzyloxy group, a lower alkanoyloxy group, a cycloalkyl group, a cycloalkyl group, an aryl group, an aralkyl group, a substituted aryl group, a heteroaryl group, a substituted heteroaryl group, a benzenesulfonyloxy group being optionally substituted by an alkyl group; a lower alkanoylamino group, a lower alkoxycarbonylamino group, a lower alkylsulfonamido group, a phthalimido group;
or R 3 is also one or more members selected from the group consisting of hydrogen, amino, alkylamino, dialkylamino, alkanoylamino, alkoxycarbonylamino, and alkylsulfonylamido;
X and Y designate lower alkyl, hydroxy lower alkyl, lower acyloxy alkyl, carbamoyloxy lower alkyl and phenyl lower alkyl, or X and Y may be linked together and then constitute, together with the nitrogen atom to which they are attached, an NXY moiety that is an optionally substituted heterocyclic ring; and
Z is selected from the group consisting of oxo, thio, seleno, telluro, and NH.