243665-90-9

Upstream product

• 77287-34-4 formamide 
• 243665-84-1 2-amino-1-(3-chloro-4-fluoro-phenyl)-4-(4-methoxy-phenyl)-1H-pyrrole-3-carbonitrile 
• 367-21-5 3-chloro-4-fluorophenylamine 
• 507273-53-2 7-(3-chloro-4-fluorophenyl)-9-(4-methoxyphenyl)tetrazolo[1,5-c]-7H-pyrrolo[3,2-e]pyrimidine 
• 75562-68-4 2-bromo-1-(p-methoxyphenyl)ethylidenemalononitrile 

Downstream Products

• 917496-20-9 2-{[7-(3-chloro-4-fluoro-phenyl)-5-(4-methoxy-phenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-ylamino]-methylene}-malonic acid diethyl ester 

Relevant academic research and scientific papers

The Gould-Jacob type of reaction for the synthesis of novel pyrimidopyrrolopyrimidines: A comparison of classical heating vs solvent free microwave irradiation

The Gould-Jacob type of reaction for the synthesis of ethyl 4-oxo-8,10-substituted-4,8-dihydropyrimido[1,2-c]pyrrolo[3,2-e] pyrimidine-3-carboxylates 5 has been carried out conventionally by the condensation between 4-aminopyrrolo[2,3-d]pyrimidines 2 and

Improved synthesis and efficient chemoselective reduction of fused tetrazoles under phase-transfer conditions

Liquid-liquid phase-transfer conditions were employed in an improved synthesis of 7,9-substituted 7H-pyrrolo[3,2-e]tetrazolo[1,5-c]pyrimidines and 5,7-substituted 4-amino-7H-pyrrolo[2,3-d]pyrimidines. The latter were obtained either by reductive ring clea

Synthesis and reactions of fluoroaryl substituted 2-amino-3- cyanopyrroles and pyrrolo[2,3-d]pyrimidines

Some fluoroaryl substituted 2-amino-3-cyanopyrroles 2 were synthesized from the reaction between (2-bromo-1-arylalkylidene)propanedinitriles 1 and fluoroaryl substituted aromatic amines under Gewald reaction condition, which on reaction with formamide and