134004-79-8

Upstream product

• 95-14-7 1,2,3-Benzotriazole 
• 55-21-0 benzamide 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 10374-25-1 N-benzoyl-1-methoxy-1-(p-methoxyphenyl)-methylamine 
• 137570-64-0 N-(ethoxy(4-methoxyphenyl)methyl)benzamide 
• 142232-49-3 5-Ethyl-4-(4-methoxy-phenyl)-2,6-diphenyl-4H-[1,3]oxazine 
• 142232-48-2 4-(4-Methoxy-phenyl)-2,6-diphenyl-4H-[1,3]oxazine 
• 142232-52-8 N-<2-benzoyl-1-(4-methoxyphenyl)-2-phenylethyl>benzamide 
• 134004-88-9 2-[Benzoylamino-(4-methoxy-phenyl)-methyl]-2-ethyl-malonic acid diethyl ester 
• 134004-87-8 2-[Benzoylamino-(4-methoxy-phenyl)-methyl]-2-methyl-malonic acid diethyl ester 
• 138768-37-3 N-[(2-hydroxynaphthalen-1-yl)(4-methoxyphenyl)methyl]benzamide 
• 138768-33-9 N-[(2-Hydroxy-4,6-dimethyl-phenyl)-(4-methoxy-phenyl)-methyl]-benzamide 
• 142232-53-9 N-<2-benzoyl-1-(4-methoxyphenyl)butyl>benzamide 

Relevant academic research and scientific papers

Cross-coupling of aromatic aldehydes with n-(Amidobenzyl)benzotriazoles: An alternative route to α-amidoketones

Background: Several transition-metal-catalyzed reactions have been used to synthesize biologically active α-amidoketones. These approaches involve inconvenient conditions or expensive catalysts. Alternative attempts based on transition-metal-free catalyst

N-(1-Benzotriazol-1-ylalkyl)amides, Versatile α-Amidoalkylation Reagents. 1. α-Amidoalkylation of CH Acids

N-(1-Benzotriazol-1-ylalkyl)amides 2, easily prepared from an amide and an aldehyde with benzotriazole, react smoothly with CH acids under mild conditions to give the α-amidoalkylation products in good yields.Benzotriazole aminals also react with CH acids in the presence of methyl iodide.