96682-72-3

Upstream product

• 120642-56-0 (Z)-1-acetyl-2-benzylideneindolin-3-one 
• 140-29-4 phenylacetonitrile 
• 69-72-7 salicylic acid 
• 95542-12-4 1-acetyl-2-benzylideneindolin-3-one 
• 127832-25-1 2-[1-Amino-1-phenyl-meth-(E)-ylidene]-1,2-dihydro-indol-3-one 

Downstream Products

• 127832-31-9 2-acetylamino-3-phenyl-4-quinolone 
• 127832-32-0 1-acetoxy-2-diacetylamino-3-phenylquinoline 
• 129207-15-4 2-morpholinoacetylamino-3-phenyl-4-quinolone 
• 129207-16-5 2-chloroacetylamino-3-phenyl-4-quinolone 
• 129226-38-6 1H-2,3-dihydro-2,9-dioxo-10-phenylimidazo<1,2-a>quinoline 
• 129207-14-3 2-amino-3-phenyl-4-chloroacetoxyquinoline hydrochloride 
• 129207-13-2 2-di(chloroacetyl)amino-3-phenyl-4-chloroacetoxyquinoline 

Relevant academic research and scientific papers

Convenient synthesis of chromones and quinolinones

A one pot synthesis of substituted chromones and quinolinones by condensing commercially available and cheaper molecules like salicylic acid and anthranilic acid respectively with alkenes / nitriles followed by insitu cyclization using ammonium acetate as base has been achieved.

NEW REARRANGEMENT OF 2-ARYLMETHYLENE-3-INDOLINONES TO 2-AMINO-3-ARYL-4-QUINOLONES AND 2-(α-AMINOARYLMETHYLENE)-3-INDOLINONES

2-Arylidene-3-indolinones are converted by the action of sodium azide in a mixture of sulfuric and acetic acids into an easily separated mixture of 2-amino-3-aryl-4-quinolones and 2-(α-aminoarylmethylene)-3-indolinones.