posted on 2019-02-08, 00:00authored byAlessio Zuliani, Prabhat Ranjan, Rafael Luque, Erik V. Van der Eycken
The
synthesis of imidazolones through the cycloisomerization of
ureas, specifically propargylureas, has gained attention due to the
large availability of starting materials. However, this type of synthesis
normally requires the utilization of strong bases, such as NaOH, expensive
homogeneous metal catalysts, such as Ag-, Au-, and Ru-based systems,
or toxic and hazardous chemicals. Herein, a study of different synthetic
routes for the preparation of imidazolones through the cycloisomerization
of propargylic ureas under fast, mild, and environmentally friendly
conditions with heterogeneous catalysis was undertaken. First, the
synthesis were carried out under mild conditions using toluene and
acetonitrile as solvents. Silver and gold nanoparticles supported
on AlSBA-15 were used as heterogeneous catalysts. The catalysts were
prepared by mechanochemical and microwave-assisted techniques. Sequentially,
a range of solvents was replaced by the greener ethanol. Finally,
all obtained results were combined in order to carry out the reaction
using only water as solvent and promoter of the reaction. Aiming to
expedite the procedure, the synthesis were carried out under conventional
and microwave irradiation.