Abstract

AbstractA novel five‐step synthesis of Boc‐3,3‐dimethylglutamic acid α‐ethyl ester 11 is reported. All the steps are high yielding and simple to carry out. By use of the 3,3‐dimethylglutamic acid building block, we successfully discovered a novel class of DPP‐IV inhibitors, Glu‐Pro‐Nitrile dipeptide mimics 2, with high potency (IC50 < 40 nM). The consequence of 3,3‐dimethyl substituent on the rate of intramolecular cyclization between N‐terminal amine and 5‐position amide bond in different buffer solutions was also evaluated.

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