54609-79-9

Upstream product

• 83-24-9 2,5-dimethyl-1-phenyl-1H-pyrrole 
• 75-36-5 acetyl chloride 
• 3240-34-4 [bis(acetoxy)iodo]benzene 
• 7294-89-5 4-(phenylamino)pent-3-en-2-one 

Downstream Products

• 54609-80-2 1-phenyl-2,5-dimethyl-3,4-di-(2-hydroxy-2-propyl)pyrrole 
• 109450-25-1 1,4,5,7-tetramethyl-6-phenyl-6H-pyrrolo[3,4-d]pyridazine 

Relevant academic research and scientific papers

Synthesis of polysubstituted pyrroles via phi(OAC)2-mediated oxidative coupling of enamine esters and ketones

Enamine esters or ketones could undergo homocoupling by the action of (diacetoxyiodo)benzene in the presence of BF3OEt2, giving rise to pyrrole products. This reaction could be used to synthesize symmetric polysubstituted pyrroles. Some asymmetric polysub

Cyclopenta[c]pyrrole derivatives

2,4,5,6-Tetrahydrocyclopenta[c]pyrrole-4-carboxamide and 4-thiocarboxamide derivatives useful as anti-secretory and anti-ulcer agents are prepared by hydrolysis or thiohydrolysis of the corresponding 2,4,5,6-tetrahydrocyclopenta[c]pyrrole-4-carbonitriles or, in the case of the thiocarboxamides, by reaction of the 4-carboxamide with phosphorus pentasulfide.