Saltar al contenido
Merck
  • Palladium-catalyzed direct heck arylation of dual pi-deficient/pi-excessive heteroaromatics. Synthesis of C-5 arylated imidazo[1,5-a]pyrazines.

Palladium-catalyzed direct heck arylation of dual pi-deficient/pi-excessive heteroaromatics. Synthesis of C-5 arylated imidazo[1,5-a]pyrazines.

Organic letters (2008-06-26)
Jian-Xin Wang, J Adam McCubbin, Meizhong Jin, Radoslaw S Laufer, Yunyu Mao, Andrew P Crew, Mark J Mulvihill, Victor Snieckus
RESUMEN

A general and efficient synthesis of 5-aryl imidazo[1,5- a]pyrazines by palladium-catalyzed coupling of the corresponding 8-substituted derivatives with aryl halides is described. The scope of this new reaction for the imidazo[1,5- a]pyrazine ring system was explored using three readily available 8-substituted precursors, X = NH2, NMe2, and OMe, as well as 8-aryl derivatives, X = Ar'. On the basis of these results as well as studies using a deuterated derivative, a Heck-like mechanism is proposed for this transformation.

MATERIALES
Referencia del producto
Marca
Descripción del producto

Sigma-Aldrich
Di-tert-butyl(methyl)phosphonium tetrafluoroborate, 97%