96138-48-6

Upstream product

• 495-69-2 Hippuric Acid 
• 626-34-6 ethyl aminocrotonate 
• 52903-67-0 4,4-Dicyano-3-methyl-but-3-en-saeure-ethylester 

Downstream Products

• 1412452-96-0 ethyl 5-benzamido-4-methyl-6-oxo-1-(p-tolyl)-1,6-dihydropyridazine-3-carboxylate 
• 1412452-99-3 ethyl 3-(6-oxo-3-phenyl-1,6-dihydro-1,2,4-triazin-5(2H)-ylidene)butanoate 
• 1412452-91-5 ethyl 2-benzylidene-3-(5-oxo-2-phenyloxazol-4(5H)-ylidene)butanoate 
• 1412452-93-7 ethyl 3-(5-oxo-2-phenyloxazol-4(5H)-ylidene)-2-(2-phenylhydrazono)butanoate 
• 1412452-94-8 ethyl 3-(5-oxo-2-phenyloxazol-4(5H)-ylidene)-2-(2-(p-tolyl)hydrazono)butanoate 
• 1412452-92-6 4-ethyl 2-methyl 3-methyl-5-phenyl-1H-pyrrole-2,4-dicarboxylate 
• 1412452-97-1 ethyl 3-(5-oxo-1,2-diphenyl-1H-imidazol-4(5H)-ylidene)butanoate 
• 1412452-98-2 ethyl 3-(5-oxo-2-phenyl-1-(p-tolyl)-1H-imidazol-4(5H)-ylidene)butanoate 

Relevant academic research and scientific papers

A simple and convenient synthesis of 4-ylidene-5(4H)oxazolone derivatives: Oxazolone ring transformation leading to other heterocyclic structures

Simple, effective, and high yield synthetic procedure for the synthesis of 4-ylidene-5(4H)-oxazolones 2a-m from arylidene-malononitriles under solvent-free conditions is described. The scope of this reaction was investigated, and it was found that the presence of anhydrous sodium acetate gave the corresponding oxazolones in excellent yields. The newly generated oxazolone derivative 2m underwent ring transformation into pyrroles, imidazoles, pyridazine, and triazines.

ETUDE DE LA REACTIVITE DU 3-AMINO-2-BUTENOATE D'ETHYLE VIS-A-VIS D'AZOLINE-5-ONES.

Various 1,3-disubstituted pyrazolin-5-ones, 3-phenylisoxazolin-5-one and 2-phenyloxazolin-5-one react with ethyl 3-amino-2-butenoate to yield compounds resulting from the elimination of ammonia between the precursors; subsequent intramolecular cyclization