87813-97-6

Upstream product

• 7151-24-8 N-Hydroxy-cis-4-cyclohexene-1,2-dicarboximide 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 621-00-1 1,3-di-p-tolylurea 
• 14034-62-9 4-methylanilinium p-toluenesulfonate 
• 1087-99-6 3-(4-methylphenyl)quinazoline-2,4(1H,3H)-dione 
• 87813-99-8 6-(3-p-Tolyl-ureido)-cyclohex-3-enecarboxylic acid p-tolylamide 
• 7255-72-3 4-chloroaniline p-toluenesulfonate 
• 1219-99-4 N,N'-bis(4-chlorophenyl)urea 
• 65441-00-1 4-amino-benzoic acid ; toluene-4-sulfonate 
• 87814-01-5 C₂₂H₂₁N₃O₆ 
• 16155-52-5 phenyl-hydrazine; toluene-4-sulfonate 
• 14034-57-2 anilinium p-tolylsulfonate 
• 102-07-8 bis(diphenyl)urea 
• 87813-98-7 6-(3-Phenyl-ureido)-cyclohex-3-enecarboxylic acid phenylamide 
• 603-23-6 3-phenyl-2,4-(1H,3H)-quinazolinedione 
• 14034-69-6 Toluene-4-sulfonic acid; compound with 4-methoxy-phenylamine 

Relevant academic research and scientific papers

Imides: Part IV - Synthesis and Reactions of N-(Arylsulphonyloxy)cyclohex-4-ene-1,2-dicarboximides

N-(Arylsulphonyloxy)cyclohex-4-ene-1,2-dicarboximides (IIa and IIb) undergo base-catalysed Lossen rearrangement with aromatic amines in refluxing ethanol to give mixtures of N-(2-arylcarbamoyl)cyclohex-4-enyl-N'-arylureas (IIIa-d) and the amine salts of arylsulphonic acids (IVa-h).Fusion of II with aromatic amines for 15 min gives mixtures of 3-arylquinazoline-2,4-diones (VIa-c) and IV; however fusion for 1 hr affords mixtures of sym-N,N'-diarylureas (VIIa-d) and IV.Compounds IIa and IIb also react with phenylhydrazine to give mixtures of VIII and phenylhydrazine saltof arylsulphonic acids (IXa and IXb).The mass spectra of IIb and IIIa are presented, and discussed.