Synthesis and characterization of new diiodocoumarin derivatives with promising antimicrobial activities

Beilstein J Org Chem. 2011:7:1688-96. doi: 10.3762/bjoc.7.199. Epub 2011 Dec 19.

Abstract

A series of 6,8-diiodocoumarin-3-N-carboxamides (4-11) were prepared. Treatment of ethyl 6,8-diiodocoumarin-3-carboxylate (1) with ethyl cyanoacetate/NH(4)OAc gave ethyl 2-(3-carbamoyl-6,8-diiodocoumarin-4-yl)-2-cyanoacetate (12) and 2-amino-4-hydroxy-7,9-diiodocoumarino[3,4-c]pyridine-1-carbonitrile (13), and treatment with acetone in the presence of NH(4)OAc or methylamine gave the ethyl 4-oxo-2,6-methano-2-methyl-3,4,5,6-tetrahydro-8,10-diiodobenzo[2,1-g]-2H-1,3-oxazocine-5-carboxylate derivatives 14a,b. All compounds were evaluated for their antimicrobial activity and the compounds 12-14a,b exhibited a pronounced effect on all tested microorganisms.

Keywords: 3,5-diiodosalicylaldehyde; Michael reaction; antimicrobial; coumarins; diethyl malonate; ethyl cyanoacetate.