Stereocomplexity and Stereoselective Synthesis of Triamine Molecules Bearing Four Chiral Carbon Centers: Stereodifferentiated Preparation of All 10 Stereoisomers of 2,6-Bis[1-(1-phenylethylamino)ethyl]pyridines

Compounds (S,S)-2,6-bis(1-hydroxyethyl)pyridine, (R,R)-2,6-bis(1-acetoxyethyl)pyridine, and (1R,1‘S)-2-(1-acetoxyethyl)-6-(1‘-hydroxyethyl)pyridine were obtained by lipase-catalyzed kinetic acetylation of
2,6-bis(1-hydroxyethyl)pyridine as enantiomerically pure forms. The stereospecific replacement of hydroxy
groups with (R)-phenylethylamine or (S)-phenylethylamine via its methanesulfonate or toluenesulfonate
simultaneously or stepwise afforded all the stereoisomers of 1. Stereospecific preparation of all the 10
possible stereoisomers of 2,6-bis[1-(1-phenylethylamino)ethyl]pyridines 1a−f was achieved. Triamine
1b reacted with ZnCl2 to form Zn−triamine complex 16, the structure of which was determined by
X-ray crystallographic analysis.