Abstract:
Silatranes bearing an amide group in the axial chain have been synthesized by the reaction of 1-(3-aminopropyl)silatrane with arylchalcogenylacetic acids (Het)ArYCH2CO2H [(Het)Ar=2-MeC6H4, 4-Cl-2-MeC6H3, 4-ClC6H4, 3-indolyl; Y=O, S], and their structures have been established by 1H,13C, 15N, 29Si NMR and IR spectroscopy. When 4-chlorophenylsulfonylacetic acid was employed, the reaction proceeded unexpectedly via the 4-chlorophenyl methyl sulfone intermediate and resulted in methyl 4-[3-(1 silatranyl)propylamino]phenyl sulfone.