Abstract
Some new 4-(1H-pyrrol-1-yl)phenyl benzoates (4a-m) were synthesized by the reaction of 4-(1H-pyrrol-1-yl)phenol (2) and substituted benzoyl chlorides (3a-m). All the synthesized compounds 4a-m were studied for their antimicrobial and antitubercular activities using standard drugs. With minimum inhibitory concentration values ranging from 0.8 to 12.5 g/mL, all of the drugs demonstrated antitubercular activity. The tested compounds exhibited substantial synthetic accessibility, docking scores, and antimicrobial activities.