Volgograd Journal of Medical Research
Quarterly Journal of Science and Practice

UDK: 547.856.1

Selective synthesis of 1-benzylquinazoline-2,4(1H,3H)-dione

A. A. Ozerov, M. S. Novikov, A. I. Luganchenko

Abstract

The reaction of 1,3-dibenzoylquinazoline-2,4(1H,3H)-dione with potassium carbonate in anhydrous DMF at room tem- perature leads to the formation of a potassium salt of 3-benzoylquinazoline-2,4(1H,3H)-dione, the alkylation of which in situ with benzyl chloride produces 1-benzyl-3-benzoylquinazoline-2,4(1H,3H)-dione. A one-pot method for the prepara- tion of N1-monosubstituted derivatives of quinazoline-2,4(1H,3H)-dione was developed. The effect of an alkaline agent on the yield and ratio of the debenzoylation products was studied.

Keywords

quinazolinedione, debenzoylation, selective alkylation, 3-benzoylquinazolinedione

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