Benzoyl Urea Derivatives

作者: Sandor Farkas , Csilla Horvath , Jozsef Nagy , Istvan Borza , Sandor Kolok

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摘要: The new benzoyl urea derivatives of formula (I) wherein the meaning X and Y independently are hydrogen atom, hydroxy, benzyloxy, amino, nitro, C1-C4 alkylsulfonamido optionally substituted with a halogen atom or atoms, alkanoylamido alkoxy, aroyl-carbamoyl alkyl alkoxycarbonyl group, neighboring groups form together one more identical different additional hetero —CH═ and/or —CH2— an 4-7 membered homo- heterocyclic ring, preferably morpholine, pyrrole, pyrrolidine, oxo- thioxo-pyrrolidine, pyrazole, pyrazolidine, imidazole, imidazolidine, thioxo-imidazole 1,4-oxazine, oxazole, oxazolidine, triazole, thioxo-oxazolidine, 3-oxo-1,4-oxazine V Z cyano, alkyl, trifluoromethyl, hydroxy esterized carboxyl W is oxygen as well alkylene, C2-C4 alkenylene, aminocarbonyl, —NH—, —N(alkyl)-, —CH2O—, —CH2S—, —CH(OH)—, —OCH2— group—, when dotted bonds ( ) represent simple C—C then U group alkylene alkenylene can further double bond in this case means electron pair, which participate optical antipodes, racemates salts thereof highly effective selective antagonists NMDA receptor, moreover most compounds antagonist NR2B subtype receptor. Furthermore objects present invention pharmaceutical compositions containing antipodes active ingredients processes for producing these compositions.

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Sandor Farkas, Attila Bielik, Gyorgy Keseru, Csilla Horvath, Jozsef Nagy, Istvan Borza, Gyorgyi Ignaczne Szendrei, Istvan Vago, Gizella Bartane Szalai, Gyorgy Domany, Sandor Kolok, Eva Kovacsne Bozo, Piperdine derivatives as NMDA receptor antagonists ,(2004)