Kinetics and mechanism of the hydrolytic degradation of indinavir: intramolecular catalysis.

ABSTRACT The pH-rate profile of first-order rate constants for the lactonization of Indinavir in aqueous solutions with ionic strength I  = 1 (KCl) at 40°C is reported. The lactonization reaction is a subject of strong buffer catalysis with a nonlinear dependence of the first-order rate constants on the concentration of the buffer. The pH-rate profile is more complex than the pH-rate profiles for the hydrolysis of simple peptides and for the intramolecular OH-catalyzed hydrolysis of γ-hydroxyamides. This complexity appears unique to Indinavir and is a result of the cis -aminoindanol leaving group. The mechanistic pathways for the lactonization are discussed. The buffer catalysis data are consistent with kinetic general acid catalysis. The second-order rate constant for the specific-acid catalyzed hydrolysis of Indinavir at 40°C ( k H  = 2.2 × 10 −4 M −1  min −1 ) is similar to that for a simple peptide indicating similar interactions in the rate limiting transition state for both reactions.