Note Synthesis and antibacterial activity of benzamides and sulfonamide derived from 2- amino-5-bromo/nitropyridine against bacterial strains isolated from clinical patients
Diwakar Rai, Ramendra K. Singh
Abstract
Diwakar Rai, Ramendra K. Singh
Abstract
A series of 5-(bromo/nitropyridin-2-yl)benzamide derivatives, viz. N-(5-bromopyridin-2-yl)benzamide 4a, 4-methyl-N-(5bromopyridin-2-yl)benzamide 4b, 4-chloro-N-(5-bromopyridin-2yl)benzamide 4c, 4-nitro-N-(5-bromopyridin-2-yl)benzamide 4d , N-(5-nitropyridin-2-yl)benzamide 7a, 4-methyl-N-(5-nitropyridin2-yl)benzamide 7b, 4-chloro-N-(5-nitropyridin-2-yl)benzamide 7c, 4-nitro-N-(5-nitropyridin-2-yl)benzamide 7c and a sulfonamide derivative, N-benzoyl-N-(5-bromopyridin-2-yl)trifluoromethane sulfonamide 5 have been synthesized as novel antibacterial agents. All compounds have shown promising activity (MIC 0.22–1.49 μM) against Gram-positive and Gram-negative bacterial strains using microdilution broth susceptibility test method. The sulfonamide 5 showed much better results than other compounds and its MIC values predicted it to be a lead compound as an antibacterial agent.
OpenAlex reports 7 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
A series of 5-(bromo/nitropyridin-2-yl)benzamide derivatives, viz. N-(5-bromopyridin-2-yl)benzamide 4a, 4-methyl-N-(5bromopyridin-2-yl)benzamide 4b, 4-chloro-N-(5-bromopyridin-2yl)benzamide 4c, 4-nitro-N-(5-bromopyridin-2-yl)benzamide 4d , N-(5-nitropyridin-2-yl)benzamide 7a, 4-methyl-N-(5-nitropyridin2-yl)benzamide 7b, 4-chloro-N-(5-nitropyridin-2-yl)benzamide 7c, 4-nitro-N-(5-nitropyridin-2-yl)benzamide 7c and a sulfonamide derivative, N-benzoyl-N-(5-bromopyridin-2-yl)trifluoromethane sulfonamide 5 have been synthesized as novel antibacterial agents. All compounds have shown promising activity (MIC 0.22–1.49 μM) against Gram-positive and Gram-negative bacterial strains using microdilution broth susceptibility test method. The sulfonamide 5 showed much better results than other compounds and its MIC values predicted it to be a lead compound as an antibacterial agent.
Key concepts: Benzamide, Sulfonamide, Chemistry, Stereochemistry, Derivative (finance), Medicinal chemistry, Economics, Financial economics