92119-01-2

Upstream product

• 50821-72-2 quinolone-4-carbonyl chloride 
• 62-53-3 aniline 
• 91-22-5 quinoline 
• 500-72-1 oxanilic acid 
• 29620-62-0 cinchoninic hydrazide 

Downstream Products

• 132346-14-6 N-[4]quinolylmethyl-aniline 
• 1220349-22-3 3-(3-methoxyphenyl)-N-phenylquinoline-4-carboxamide 
• 1220349-24-5 3-(naphthalen-2-yl)-N-phenylquinoline-4-carboxamide 
• 1220349-23-4 3-(2-methoxyphenyl)-N-phenylquinoline-4-carboxamide 
• 1220349-25-6 3-(phenanthren-9-yl)-N-phenylquinoline-4-carboxamide 
• 1220349-11-0 N-phenyl-3-(p-tolyl)quinoline-4-carboxamide 
• 1220349-21-2 3-(4-fluorophenyl)-N-phenylquinoline-4-carboxamide 
• 1522465-07-1 3-(5-methylthiophen-2-yl)-N-phenylquinoline-4-carboxamide 

Relevant academic research and scientific papers

Silver-catalyzed direct C-H oxidative carbamoylation of quinolines with oxamic acids

A silver-catalyzed efficient and direct C-H carbamoylation of quinolines with oxamic acids to access carbamoylated quinolines has been developed through oxidative decarboxylation reaction. The reaction proceeds smoothly over a broad range of substrates wi

Pd0/PR3-catalyzed arylation of nicotinic and isonicotinic acid derivatives

(Chemical Eqation Presented) Good for your health: Intermolecular C-H functionalization of pyridine rings at the 3- and 4-positions is described using a Pd0/PR3/ArBr catalytic system. This reaction provides a powerful method for the preparation of structurally diverse nicotinic and isonicotinic acids that are of great importance in drug discovery.