37118-73-3

Upstream product

• 37118-72-2 4-(p-methoxyphenyl)-2-(1H)-quinolinone 
• 100-07-2 4-methoxy-benzoyl chloride 
• 2881-83-6 ethyl 4-methoxybenzoylacetate 
• 62-53-3 aniline 
• 100-09-4 4-methoxybenzoic acid 
• 37118-72-2 2-hydroxy-4-(4-methoxyphenyl)quinoline 
• 965-01-5 3-(4-methoxyphenyl)-3-oxo-N-phenylpropanamide 
• 610-14-0 2-nitrobenzyl chloride 
• 36188-55-3 N-(2-(4-methoxybenzoyl)phenyl)acetamide 
• 36192-61-7 2-amino-4'-methoxybenzophenone 
• 73376-03-1 (4-methoxyphenyl)(2-nitrophenyl)methanone 
• 552-16-9 ortho-nitrobenzoic acid 

Downstream Products

• 106015-61-6 2-(4-Ethyl-piperazin-1-yl)-4-(4-methoxy-phenyl)-quinoline 
• 106015-78-5 2-{4-[4-(4-Methoxy-phenyl)-quinolin-2-yl]-piperazin-1-yl}-ethanol 
• 120301-15-7 4-(4-Methoxy-phenyl)-2-piperazin-1-yl-quinoline 

Relevant academic research and scientific papers

A Facile Synthesis of 5-Phenyl-Dibenzo[b, g][1,8]Napthyridines

The Vilsmeier Haack heterocyclization of 2-aryl amino-4-phenyl quinolines quinoline yielded the hitherto unknown 5-phenyl-dibenzo[b,g][1,8]naphthyridines in quantitative yield. The synthesis of aryl amines was achieved by the action of anilines on 2-chloro-4-phenyl quinoline, which in turn was sourced through the combes reaction of benzoyl acetanilides.