American Chemical Society, Journal of Organic Chemistry, 6(73), p. 2473-2475, 2008
DOI: 10.1021/jo7026883
Wiley-VCH Verlag, ChemInform, 30(39), 2008
Full text: Unavailable
A novel and simple method of preparation of 2-alkylaminoquinazolin-4-ones with fused heteroaromatic rings from easily accessible (hetero)aromatic amines is described. The method is very efficient, and the 2-alkylaminoquinazolinone derivatives are obtained in three steps without chromatographic purification. The key step is the ring closure of the N-protected guanidine intermediates by intramolecular Friedel-Craft's type substitution.