78893-71-7

Upstream product

• 100-63-0 phenylhydrazine 
• 2902-98-9 2-chloro-2,2-diphenylacetyl chloride 
• 3321-83-3 benzilic acid phenylhydrazide 

Downstream Products

• 94941-18-1 1-(N-acetyl-N-phenyl)amino-3-phenyloxindole 
• 78893-73-9 Acetic acid 1-(acetyl-phenyl-amino)-3-phenyl-1H-indol-2-yl ester 
• 94941-28-3 1-(N-Methyl-N-phenylamino)-3-methyl-3-phenyloxindole 
• 78893-72-8 1-(N-benzoyl-N-phenyl)amino-3-phenyl-2,3-dihydro-2-indolone 

Relevant academic research and scientific papers

CONVERSIONS OF 1-ARYLAMINO-3-PHENYLOXINDOLES

Acylation of 1-arylamino-3-phenyloxindoles by acetic anhydride in the presence of an acidic catalyst (TsOH) gives N-acetyl derivatives; alkylation by methyl iodide in the presence of sodium ethoxide gives C(3)- and N-dimethyl derivatives.Reduct

1-Arylamino-3-phenyl-2,3-dihydro-2-indolones

α-Chlorodiphenylacetyl chloride reacts with arylhydrazines to give 1-arylamino-3-phenyl-2,3-dihydro-2-indolones, which undergo acetylation at the nitrogen and oxygen and undergo benzoylation at the nitrogen atom.