Synthesis of 1,2,4-oxadiazole-linked orthogonally urethane-protected dipeptide mimetics

The synthesis of a new class of 1,2,4-oxadiazole-linked orthogonally urethane-protected dipeptide mimetics is described. The protocol employs a reaction between an N-protected amino acyl fluoride and an amino acid-derived amidoxime. All the three commonly employed urethanes have been used in this protocol for N-protection. The course of the reaction was found to be high yielding and all new compounds were well characterized by NMR and mass spectroscopy. The O-acyl amidoxime intermediate has also been isolated as a stable solid.

A new class of 1,2,4-oxadiazole-linked orthogonally urethane-protected dipeptide mimetics has been synthesized by reaction between an N-protected amino acyl fluoride and an amino acid-derived amidoxime.