808750-47-2Relevant academic research and scientific papers
Suzuki reaction on pyridinium N-(5-bromoheteroar-2-yl)aminides
José Reyes,Luisa Izquierdo,Alvarez-Builla, Julio
, p. 8713 - 8715 (2004)
The Suzuki cross-coupling reaction takes place efficiently on bromoaminides 3 (5) employing Cs2CO3 as base and Pd(PPh 3)4 as catalyst, yielding mono- and di-coupled products 4 (6). The reactivity of substituted
A facile synthesis of 3,5-halo and aryl 1H-pyridin-2-ones from pyridinium N-(pyridin-2-yl)aminide
Filace, Fabiana,Sucunza, David,Izquierdo, M. Luisa,Burgos, Carolina,Alvarez-Builla, Julio
, p. 6088 - 6094 (2013/07/19)
The synthesis of halogenated and arylated 1H-pyridin-2-ones starting from pyridinium N-(pyridin-2-yl)aminides is described. The synthetic pathway involves the reaction of pyridinium N-(5-bromopyridin-2-yl)aminide, N-(3-bromo-5- chloropyridin-2-yl)aminide or N-(3,5-dibromopyridin-2-yl)aminide with different boronic acids to afford monosubstituted and disubstituted aminides in good yields. An additional bromination in the 3-position of N-(5-arylpyridin-2-yl) aminides was performed. Finally, reduction of the N-N bond followed by the reaction of the corresponding 2-aminopyridines with sodium nitrite/sulfuric acid in water yields 3,5-disubstituted 1H-pyridin-2-ones in good yields.
Suzuki reaction on pyridinium N-haloheteroarylaminides: regioselective synthesis of 3,5-disubstituted 2-aminopyrazines
Castillo, Rafael,Reyes, M. José,Izquierdo, M. Luisa,Alvarez-Builla, Julio
, p. 1351 - 1370 (2008/09/18)
An extensive study of Suzuki-Miyaura cross-coupling processes on N-pyridinium bromoazinyl aminides has been performed. Mono- and disubstitution on 5- and 3,5-bromo derivatives produced the corresponding aryl derivatives. In the disubstituted compounds reg
