Amide derivatives as NMDA receptor antagonists

   
   

New Formula (I) compounds are disclosed having NR2B selective NMDA receptor antagonist activity: ##STR1##

wherein

    • one of the neighboring R1, R2, R3 and R4 groups is OH or NH2 and the others are each hydrogen , or
    • two of the neighboring R1, R2 R3 and R4 groups in given case together with one or more identical or different additional hetero atom and -CH and/or -CH2- groups forms a 5-6 membered homo- or heterocyclic ring, preferably pyrrole, pyrazole, imidazole, oxazole, oxo-oxazolidine, or 3-oxo-1,4-oxazine ring, and the other two of R1, R2, R3 and R4 groups are hydrogen atoms,
    • R5 and R6 together with the nitrogen between them form a saturated or unsaturated, 4-6 membered heterocyclic ring, which is substituted by hydroxy group, and/or in given case phenyl or phenoxy, phenyl-(C1-C4 alkyl), phenyl-(C1-C4 alkoxy), phenoxy-(C1-C4 alkyl), anilino, phenyl-(C1-C4 alkylamino), [phenyl-(C1-C4 alkyl)]-amino, benzoyl, hydroxy-diphenylmethyl, C1-C4 alkoxycarbonyl-phenoxymethyl or benzhydrylidene group, optionally substituted on the aromatic ring by one or more halogen atom, cyano or hydroxy group, C1-C4 alkyl or C1-C4 alkoxy group,
    • X is independently oxygen, -NH- or a CH2 group,
    • Y is independently a nitrogen atom or a -CH- group, and the salts thereof formed with acids and bases.
  •  
    Web www.patentalert.com

    < Aza-and polyaza-naphthalenyl-carboxamides useful as HIV integrase inhibitors

    < Pyrazolopyridinyl pyridine and pyrimidine therapeutic compounds

    > N-substituted heterocyclic amines as modulators of chemokine receptor activity

    > Azabicyclic-substituted-heteroaryl compounds for the treatment of disease

    ~ 00194