New features in synthesis of talampanel related 2,3-benzodiazepines
Sándor Sólyom1, István Pallagi, Gizella Abrahám
1IVAX Drug Research Institute Ltd., H-1045 Budapest, Berlini u. 47-49, Hungary. sandor.solyom@idri.hu
Abstract:
Analogues of talampanel (1), a highly active AMPA antagonist 2,3-benzodiazepine, were synthesized, where the characteristic amino-function was either transposed or sterically shielded. For the key intermediates (hemiketals 6a, b) a new synthetic method of different mechanism was developed. The inactivity of several new compounds indicates the significance of the 4-amino(phenyl) function in BDZs of type 1.
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