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was obtained by the condensation of ethyl α-cyano-β-(2-furyl)acrylate with p-fluorophenylmagnesium bromide. Its deethoxycarbonylation led to β-(p-fluorophenyl)-β-(2-furyl)propionitrile. Reduction of the nitrile with lithium aluminum hydride gave γ-(p-fluorophenyl)-γ-(2-furyl)propylamine. Some transformations of the latter were studied.

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Synthesis and Pharmacological Activity of N-[β-(para-Substituted Benzoyl)ethyl]isoleucine and -methionine. -Most of the amino acid derivatives prepared (III) possess antiinflammatory activity. -(AGABABYAN, A. G.; ISAKHANYAN, A. U.; PAPOYAN, O. A.; TUMADZHYAN, A. E.; BALASANYAN, A. S.; GEVORGYAN, G. A.; Khim.-Farm.