Rs. Atkinson et al., -ACETOXYAMINO-2-TRIFLUOROMETHYLQUINAZOLIN-4(3H)ONE AS AN AZIRIDINATING AGENT FOR ALKENES, Journal of the Chemical Society, Chemical Communications, (15), 1993, pp. 1215-1216
The title compound 4, prepared by lead tetraacetate oxidation of 5, is
stable at room temperature and aziridinates alkenes in better yield a
nd higher diastereoselectivity than, e.g. the 2-ethyl compound 1; hydr
azinolysis of the quinazolinone ring in 20 gives the corresponding N-a
minoaziridine 21 in 64% yield.