PREPARATION AND ANTICONVULSANT ACTIVITY OF A SERIES OF FUNCTIONALIZED ALPHA-AROMATIC AND ALPHA-HETEROAROMATIC AMINO-ACIDS

We recently reported the potent anticonvulsant activity of (R,S)-α-acetamido-N-benzyl-α-phenylacetamide (2b). Selectively substituted derivatives of this compound have now been prepared (23 examples) and evaluated in the maximal electroshock seizure (MES) and horizontal screen (tox) tests in mice. In several key cases, replacement of the α-phenyl substituent in 2b by a relatively small, electron-rich, heteroaromatic moiety led to a substantial improvement in the anticonvulsant potency of the drug candidate. The most active compounds were (R,S)-α-acetamido-N-benzyl-2-furanacetamide (2g) and (R,S)-α-acetamido-N-benzyl-2-pyrroleacetamide (2i). After ip administration, the MES ED 50 values for 2g (10.3 mg/kg) and 2i (16.1 mg/kg) compared well with phenytoin (9.50 mg/kg). Evaluation of the two individual enantiomers of 2g demonstrated that the anticonvulsant activity resided in the R stereoisomer. The low ED 50value (3.3 mg/kg) for (R)-2g contributed to the large protective index (TD 50/ED50) observed for this drug candidate, which approached that of phenytoin. © 1990, American Chemical Society. All rights reserved.