1422975-81-2

Upstream product

• 7677-24-9 trimethylsilyl cyanide 
• 1220960-48-4 4,6-dimethoxy-3-(4-methylphenyl)-1H-indole-7-carbaldehyde 

Downstream Products

• 1422975-90-3 N-(2-(4,6-dimethoxy-3-(p-tolyl)-1H-indol-7-yl)-2-oxoethyl)-acetamide 
• 1422975-94-7 5-(4,6-dimethoxy-3-(p-tolyl)-1H-indol-7-yl)-2-methyloxazole 
• 1422975-96-9 N-(2-(4,6-dimethoxy-3-(p-tolyl)-1H-indol-7-yl)-2-oxoethyl)-4,6-dimethoxy-3-(p-tolyl)-1H-indole-7-carboxamide 
• 1422975-98-1 2,5-bis-(4,6-dimethoxy-3-(p-tolyl)-1H-indol-7-yl)-oxazole 
• 1422975-85-6 4,6-dimethoxy-3-(p-tolyl)-1H-indol-7-carbonyl cyanide 

Relevant academic research and scientific papers

Synthesis of 5-(7′-indolyl)oxazoles and 2,5-di-(7′-indolyl) oxazoles

The synthesis of 7-aminoacetylindoles was achieved via the hydrogenation of 7-acylcyanides, which were produced through the oxidation of indole-7-cyanohydrin silylether intermediates. 7-Oxotryptamines were subsequently converted into 5-(7′-indolyl)oxazole