Synthèse des molécules à activités biologique et thérapeutique par des catalyseurs nanostructurés
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Abstract
Propargylamines and pyrroles are very interesting intermediates molecules; they exhibit biological
and therapeutic activity. They are well known as neurodegenerative drugs. These molecules exhibit
different biological activities such as anti-inflammatory, anti-HIV and others. The synthesis method of
these molecules involves the use of metallic and non-metallic catalysts. The synthesis methods described
in the bibliography have shown that metal phosphate catalysts have not been used in the synthesis of
propargylamines and pyrroles. In our thesis, we prepared nanostructured FePO4 and FeCuP2 catalysts via
one-pot hydrothermal method. The prepared catalysts were characterized by different methods such as
UV-Vis, IR, SEM, EDX, Raman, and TEM. The characterization results confirmed the nanoscale
structure of the prepared catalysts. The catalysts FePO4 and FeCuP2 were used in the synthesis of
propargylamines by the A3 coupling of an aldehyde, an alkyne and an amine, and by the AHA coupling
of an amine, an alkyne and diiodomethane. Both catalysts exhibit good activity and stability with
propargylamine yields ranging between 50-100%. For the synthesis of pyrroles, the FeCuP2 catalyst
showed good activity in the four components reaction of aldehyde, amine, nitroalkane and ethyl
acetoacetate. Thus, a reaction mechanism was proposed in the presence of these nanostructures. The
synthesized propargylamines and pyrroles have good biological activity, they demonstarted an anti inflammatory and anti-oxidants activity. Propargylamines have therapeutic activity against Alzheimer's
disease; this study is carried out theoretically by molecular docking.
