Abstract
The chemical performance of 5-bromo-2-(bromoacetyl)-thiophene (1) was tested toward the reaction with numerous bi-nucleophilic reagents (namely; 2-aminobenzothiazoles, 2-aminothiazole, 2-aminotetrazole, 2-aminotriazole, 2-aminopyridines, 2-aminobenzimidazole ando-phenylenediamine). Therefore, a series of bridged nitrogen heterocycles bearing thiophene moiety3,5,7,9,11,13and15, respectively was synthesized. In addition, the reaction of 5-bromo-2-(bromoacetyl)-thiophene with the thiocarbamoyl compounds17,19and/or24afforded the corresponding thienyl-thiazoles18or dithien-2-yl ketones20and25, based on the reaction conditions. Treatment of1with 2-mercapto-4,6-dimethylnicotinonitrile was achieved to obtain the target dithien-2-yl ketone28. The new synthesized scaffolds were examined for their antioxidant activity by means of ABTS antioxidant assay. The thienyl-thiazole scaffold18cand 2-((2-[thiophen-2-yl]-2-oxoethyl)thio)nicotinonitrile derivative27displayed a reasonable radical scavenging activity.