74620-65-8

Upstream product

• 56177-37-8 1-(4-nitrophenyl)-2-(p-tolylsulfonyloxy)ethanone 
• 106-47-8 4-chloro-aniline 
• 118985-14-1 p-nitrophenacyl m-nitrobenzenesulphonate 
• 118985-13-0 p-nitrophenacyl p-chlorobenzenesulphonate 
• 115400-13-0 p-nitrophenacyl benzenesulphonate 
• 99-81-0 4-Nitrophenacyl bromide 

Downstream Products

• 88502-29-8 ethyl 1-(4-chlorophenyl)-2-methyl-5-(4-nitrophenyl)pyrrole-3-carboxylate 
• 88502-16-3 ethyl 1-(4-chlorophenyl)-2-methyl-4-(4-nitrophenyl)-1H-pyrrole-3-carboxylate 
• 97814-20-5 1-(4-Chloro-phenyl)-4-(4-nitro-phenyl)-1H-imidazole 
• 88502-45-8 5-(4-Amino-phenyl)-1-(4-chloro-phenyl)-2-methyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 88502-67-4 1-(4-chlorophenyl)-2-methyl-4-(4-nitrophenyl)pyrrole-3-carboxylic acid 

Relevant academic research and scientific papers

A one-pot and three-component synthetic approach for the preparation of asymmetric and multi-substituted 1,4-dihydropyrazines

An efficient, one-pot and three-component synthesis of a new series of 2-acyl-3,4,6-triaryl-1,4-dihydropyrazines is described. This two-step strategy involves treatment of phenacyl bromides and anilines to give the nucleophilic substitution intermediate f

Synthesis, Characterization, and Antibacterial Activity of Some Novel Substituted Imidazole Derivatives via One-pot Three-Component

A simple and highly efficient one-pot, three-component synthesis of novel substituted imidazole derivatives has been reported by the reaction of 3-(2-bromoacetyl)-2H-chromen-2-one, ammonium thiocyanate, and phenacyl aniline in the presence of acetic acid

Nucleophilic Substitution Reactions of Phenacyl Benzenesulphonates with Anilines in Methanol-Acetonitrile Mixtures

The nucleophilic substitution reactions of phenacyl benzenesulphonates with anilines in methanol-acetonitrile have been studied.A stronger nucleophile was found to cause less bond cleavage, while a better leaving group led to less bond formation, in compl

The Color of N-(4-Nitrophenacyl)arylamines

The N-(4-nitrophenacyl)arylamines 5, prepared from the arylamines 3 and 4-nitrophenacyl bromide (2), have a yellow, red or violet color, depending on the nature of the aryl substituents.The color is explained by intramolecular interaction of the electron accepting nitrobenzoyl group and the electron donating arylamine part of the molecules.On acetylation of the amino group the color is lost.There are no indications for an equilibrium between the amines 5 and N-(4-nitrostyryl)-arylamines 7.