38346-22-4Relevant articles and documents
N-Arylation of 4-fluoro-5-trimethylsilyl-1H-pyrazole
Hanamoto, Takeshi,Iwamoto, Yuhko,Yamada, Kenji,Anno, Ryoko
, p. 1126 - 1130 (2007)
The 1,3-dipolar cycloaddition reaction of fluoro(trimethylsilyl)acetylene prepared in situ with an excess of diazomethane smoothly proceeded to give the corresponding 4-fluoro-5-trimethylsilyl-1H-pyrazole in 84% yield. The copper iodide-catalyzed N-arylation of the fluorinated pyrazole with a variety of aryl iodides afforded N-aryl-4-fluoropyrazoles as desilylation products in good to excellent yields.