Palladium-Catalysed Amination of Aryl- and Heteroaryl Halides Using<i>tert</i>-Butyl Tetraisopropylphosphorodiamidite as an Easily Accessible and Air-Stable Ligand
作者:Gheorghe-Doru Roiban、Gerlinde Mehler、Manfred T. Reetz
DOI:10.1002/ejoc.201301789
日期:2014.4
phosphorus compound tert-butyl tetraisopropylphosphorodiamidite, prepared from bis(diisopropylamino)chlorophosphine, is an excellent ligand for palladium-catalysed Buchwald–Hartwig amination of aryl- and heteroaryl chlorides and bromides. Based on its ready accessibility and air-stability, this amination protocol is a practical approach to the synthesis of industrially important aryl- and heteroarylamines.
A synthetic strategy has been developed for the synthesis of 2‐dialkylaminoquinolines from easily available quinoline N‐oxides, tertiaryamines, diisopropyl H‐phosphonate and carbon tetrachloride (CCl4) in one pot under metal‐free conditions at room temperature.