102101-13-3

Upstream product

• 17823-58-4 ethyl 2-cyano-3,3-di(methylsulfanyl)acrylate 
• 106-47-8 4-chloro-aniline 

Downstream Products

• 91190-04-4 (E)-3-(Benzimidoyl-amino)-3-(4-chloro-phenylamino)-2-cyano-acrylic acid ethyl ester 
• 158590-96-6 5(3)-Amino-3(5)-<(4-chlorphenyl)amino>pyrazol-4-carbonsaeure-ethylester 
• 90832-89-6 4-Chloro-6-(4-chloro-phenylamino)-2-phenyl-pyrimidine-5-carboxylic acid ethyl ester 
• 90832-86-3 4-Amino-6-(4-chloro-phenylamino)-2-phenyl-pyrimidine-5-carboxylic acid ethyl ester 
• 90832-83-0 4-(4-Chloro-phenylamino)-6-hydroxy-2-phenyl-pyrimidine-5-carbonitrile 

Relevant academic research and scientific papers

Convenient synthesis of ketene N, S-acetal from low nucleophilic arylamine

Novel ketene N, S-acetals compounds were prepared by the reaction of ethyl 2-cyano-3,3-bis(methylthio)acrylate and 2-cyano-3,3- bis(methylthio)acrylonitrile with low nucleophilic aromatic amines in two convenient methods, respectively.

Highly selective and efficient synthesis of 3-arylamino-substituted 5-aminopyrazole-4-carboxylates under microwave irradiation

An improved microwave-assisted method was developed for the preparation of ethyl 5-aminopyrazole carboxylates from ethyl 2-cyano-3-methylthioacrylates and hydrazine. It was shown that using microwave irradiation significantly reduced the reaction time and improved the process selectivity and yield. The reaction proved to be reproducible in different microwave reactors and on large scale, affording the desired products in high yields and purity. A representative library of 3-arylamino-substituted 5-aminopyrazole-4-carboxylates was successfully prepared to assess the scope of the method.