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Synthesis of Quinolines and Pyrido[3,2- g or 2,3- g]quinolines Catalyzed by Heterogeneous Propylphosphonium Tetrachloroindate Ionic Liquid.

Mahboobeh AziziMahboobeh Nasr-EsfahaniIraj Mohammadpoor-BaltorkMajid MoghadamValiollah MirkhaniShahram TangestaninejadReza Kia
Published in: The Journal of organic chemistry (2018)
This report explains an efficient method for synthesis of an array of quinolines via the reaction of 2-aminoaryl ketones with terminal and internal alkynes in the presence of propylphosphonium tetrachloroindate ionic liquid supported on nanosilica (PPInCl-nSiO2) as a heterogeneous and reusable catalyst under solvent-free conditions. Inspired by this catalytic system, the first easy one-step synthesis of symmetric and unsymmetric pyrido[3,2- g or 2,3- g]quinolines was investigated through the reaction of diaroylphenylenediamines with one alkyne or two different alkynes.
Keyphrases
  • ionic liquid
  • room temperature
  • atomic force microscopy
  • metal organic framework