All of the compounds exhibited better activity (except compound 3c) than the corresponding sulfonamide derivatives.
📌 3 Key Takeaways
🎯
Objective & Hypothesis:Six new 4-amino-N-heteroaryl,N-[(2-phenyl-4H-1-benzopyran-4- oxo-6-yl)metil]benzensulfonamide derivatives, (3a-3f) were prepared by reacting 6-bromomethylflavone with the corresponding sulfonamide derivatives and their antimicrobial activities against Escherichia coli were evaluated.
📊
Key Findings & Data:Six new 4-amino-N-heteroaryl,N-[(2-phenyl-4H-1-benzopyran-4- oxo-6-yl)metil]benzensulfonamide derivatives, (3a-3f) were prepared by reacting 6-bromomethylflavone with the corresponding sulfonamide derivatives and their antimicrobial activities against Escherichia coli were evaluated.
💡
Conclusion & Impact:All of the compounds exhibited better activity (except compound 3c) than the corresponding sulfonamide derivatives.
Six new 4-amino-N-heteroaryl,N-[(2-phenyl-4H-1-benzopyran-4- oxo-6-yl)metil]benzensulfonamide derivatives, (3a-3f) were prepared by reacting 6-bromomethylflavone with the corresponding sulfonamide derivatives and their antimicrobial activities against Escherichia coli were evaluated. All of the compounds exhibited better activity (except compound 3c) than the corresponding sulfonamide derivatives.
Özet
Six new 4-amino-N-heteroaryl,N-[(2-phenyl-4H-1-benzopyran-4- oxo-6-yl)metil]benzensulfonamide derivatives, (3a-3f) were prepared by reacting 6-bromomethylflavone with the corresponding sulfonamide derivatives and their antimicrobial activities against Escherichia coli were evaluated. All of the compounds exhibited better activity (except compound 3c) than the corresponding sulfonamide derivatives.
KILCIGİL, G. A., DÜNDAR, O. B., ERTAN, R. (2003). Synthesis and Antimicrobial Testing of Some Flavonylsulfonamide Derivatives. Turkish Journal of Chemistry, Cilt: 27 - Sayı: 4, 461–466. https://ajindex.com/articles/382298