Background:
Quinolines represent an important class of bioactive molecules which are present in
various synthetic drugs, biologically active natural compounds and pharmaceuticals. Quinolines find their potential
applications in various chemical and biomedical fields. Thereby, the demand for more efficient and simple
methodologies for the synthesis of quinolines is growing rapidly.
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Objective: The green one-pot Friedlander Synthesis of Functionalized Quinolines has been demonstrated by
using graphene oxide as a carbocatalyst.
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Method: The graphene oxide catalyzed condensation reaction of 2–aminoaryl carbonyl compounds with different
cyclic/ acyclic/ aromatic carbonyl compounds in methanol at 70°C affords different quinoline derivatives.
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Results: The reaction has been examined in different protic and aprotic solvents and the best yield of quinoline
is observed in methanol at 70°C.
Conclusion:
The present method of quinoline synthesis offers various advantages over other reported methods
such as short reaction time, high yield of product, recycling of catalyst and simple separation procedure. The
graphene oxide carbocatalyst can be easily recovered from the reaction mixture by centrifugation and then can
be reused several times without any significant loss in its activity.
Tetra-Aza-Pentacenes by means of a One-Pot Friedländer Synthesis
