134004-84-5

Upstream product

• 60-35-5 acetamide 
• 95-14-7 1,2,3-Benzotriazole 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 134004-98-1 2-[Acetylamino-(4-methoxy-phenyl)-methyl]-2-ethyl-malonic acid diethyl ester 
• 134004-97-0 2-[Acetylamino-(4-methoxy-phenyl)-methyl]-2-methyl-malonic acid diethyl ester 
• 138768-31-7 N-[(4-Hydroxy-phenyl)-(4-methoxy-phenyl)-methyl]-acetamide 
• 1080529-44-7 N-[(1H-indol-3-yl)(4-methoxyphenyl)methyl]acetamide 
• 1080529-51-6 N-[(4-methoxyphenyl)(2-methyl-1H-indol-3-yl)methyl]acetamide 
• 1080529-67-4 N-[(4-methoxyphenyl)(4-methyl-1H-indol-3-yl)methyl]acetamide 
• 1080529-54-9 N-[(4-methoxyphenyl)(2-phenyl-1H-indol-3-yl)methyl]acetamide 
• 1080529-59-4 N-[(1-benzyl-1H-indol-3-yl)(4-methoxyphenyl)methyl]acetamide 
• 1080529-66-3 N-[(4-methoxyphenyl)(5-methyl-1H-indol-3-yl)methyl]acetamide 
• 137570-68-4 N-[Isopropoxy-(4-methoxy-phenyl)-methyl]-acetamide 

Relevant academic research and scientific papers

Synthesis of 3-indolylarylmethanamides by samarium triiodide catalyzed Friedel-Crafts amidoalkylation

The amidoalkylation of indoles with N-(α-benzotriazol-1-ylalkyl) amides was smoothly realized with samarium triiodide as a catalyst to give a series of novel 3-indolyl arylmethanamides with good yields and selectivities. Georg Thieme Verlag Stuttgart.

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.