359458-02-9

Upstream product

• 21815-91-8 3-chlorobenzo[b]thiophen-2-carbonyl chloride 
• 216985-67-0 2-(3-chlorobenzo[ b]thiophene-2-carboxamido)acetic acid 
• 555-16-8 4-nitrobenzaldehdye 

Downstream Products

• 1352051-66-1 N-[2-(3-chloro-1-benzo[b]thiophen-2-yl)-4-(4-nitrobenzylidene)-5-oxo-4,5-dihydro-1H-imidazol-1-yl]benzo[b]benzo[b]furan-2-carboxamide 
• 1352051-49-0 1-(3-chloro-4-fluorophenyl)-2-(3-chlorobenzo[ b]thiophen-2-yl)-4-(4-nitrobenzylidene)-1H-imidazol-5(4H)-one 
• 359006-54-5 2-(3-chlorobenzo[b]thiophen-2-yl)-4-(4-nitrobenzylidene)-1-p-tolyl-1H-imidazol-5(4H)-one 
• 1352051-53-6 1-(4-acetylphenyl)-2-(3-chlorobenzo[b]thiophen-2-yl)-4-(4-nitrobenzylidene)-1H-imidazol-5(4H)-one 
• 1352051-78-5 3-(3-chlorobenzo[b]thiophen-2-yl)-2-(4-fluorophenyl)-5-(4-nitrobenzylidene)-1,2-dihydro-1,2,4-triazin-6(5H)-one 
• 1352051-87-6 1-acetyl-3-(3-chlorobenzo[b]thiophen-2-yl)-2-(4-fluoro-phenyl)-5-(4-nitrobenzylidene)-1,2-dihydro-1,2,4-triazin-6(5H)-one 
• 1352051-58-1 2-(3-chlorobenzo[b]thiophen-2-yl)-4-(4-nitrobenzylidene)-1-(4-nitrophenyl)-1H-imidazol-5(4H)-one 
• 1352051-62-7 3-chloro-N-[2-(3-chloro-1-benzo[b]thiophen-2-yl)-4-(4-nitrobenzylidene)-5-oxo-4,5-dihydro-1H-imidazol-1-yl]benzo[b]thiophene-2-carboxamide 
• 1352051-74-1 3-(3-chloro-1-benzo[b]thiophen-2-yl)-5-(4-nitrobenzylidene)-2-phenyl-1,2-dihydro-1,2,4-triazin-6(5H)-one 
• 1352051-83-2 1-acetyl-3-(3-chloro-1-benzothiophen-2-yl)-5-(4-nitrobenzylidene)-2-phenyl-1,2-dihydro-1,2,4-triazin-6(5H)-one 
• 359610-36-9 2-(3-chlorobenzo[b]thiophen-2-yl)-1-(4-fluorophenyl)-4-(4-nitrobenzylidene)-1H-imidazol-5(4H)-one 

Relevant academic research and scientific papers

Synthesis and antimicrobial activity of oxazolone, imidazolone and triazine derivatives containing benzothiophene

3-Chloro-1-benzothiophene-2-carbonylchloride (1) was allowed to react with glycine to give 3-chloro-1-benzothiophen-2-yl-carbonylaminoacetic acid (2). Various aldehydes were treated with compound (2) in acetic anhydride to get 1,3-oxazol-5-ones (3a-d). Th

Synthesis and antimicrobial activity of oxazolone, imidazolone and triazine derivatives containing benzothiophene

3-Chloro-1-benzothiophene-2-carbonyl chloride 1 was reacted with glycine in acetone to give 3-chloro-1- benzothiophen-2-yl-carbonylaminoacetic acid 2. Various aldehydes on treatment with compound 2 in acetic anhydride to gave 1,3-oxazol-5-ones