199684-22-5

Upstream product

• 63158-35-0 1-(1-methyl-4-nitro-pyrrol-2-yl)-ethanone 
• 108-98-5 thiophenol 
• 199684-03-2 2-acetyl-5-bromo-1-methyl-4-nitropyrrole 

Downstream Products

• 248245-29-6 2-acetyl-4-azido-1-methyl-5-phenylthiopyrrole 
• 882-33-7 diphenyldisulfane 
• 248245-26-3 2-acetyl-4-amino-1-methyl-5-phenylthiopyrrole 

Relevant academic research and scientific papers

Pyrrolo[2,3-b][1,4]benzothiazine. A new ring system from azidopyrroles

Nucleophilic substitutions in pyrrole series by uncharged nucleophiles, represented a valuable and versatile method to synthesize different types of key intermediates such as compounds (6), that were used to prepare the corresponding azides (10) which by thermal decomposition afforded the title ring system (11).

Nucleophilic reactions in the pyrrole series: Displacement of halogen as a tool to functionalize the pyrrole nucleus

Nucleophilic substitutions on halopyrroles by charged and neutral carbon, nitrogen, oxygen and sulfur nucleophiles are reported. Such reactions represent a valuable and versatile instrument to prepare a wide variety of functionalized pyrroles and to obtain building blocks for the synthesis of polycyclic systems.