Stable hemiaminals from axially chiral pyridine compounds

Abstract

AbstractIn this study, we have synthesized a series of 3‐(pyridin‐2‐yl)‐2‐(pyridin‐2‐ylimino)thiazolidin‐4‐ol derivatives regioselectively from 2‐iminothiazolidin‐4‐ones using LiAlH4 at room temperature. Due to the presence of the restricted rotation around the N3‐Caryl single bond, the formation of M/P isomers was observed. The OH group of the hemiaminal was found to orient itself on the same side with pyridyl nitrogen during this restricted rotation to form an intramolecular hydrogen bond, which was demonstrated by the computational DFT study. This orientation presumably inhibited the occurrence of dehydration and stabilized the molecule.