Affiliation:
1. Department of Chemistry, Yasouj University, P. O. Box 353, Yasouj 75918-74831, Iran
Abstract
Background:
Carbon-based materials, due to their unique properties such as lightweight,
different forms, doping capability with hetero atoms, low cost, and ease of processability,
are suitable support, for heterogeneous catalysts. Among them, cellulose, as one of the most abundant
and renewable organic polymers, preserves a key position in many organic raw materials.
Pyranopyrimidine derivatives, due to their high biological activity are of interest to both medicinal
chemists and biochemists. Moreover, they play the most fundamental structural role in many natural
compounds and are medicinally useful molecules. Owing to the great variety of biologically
active pyridines, it is not surprising that the pyridine ring system has become a vital basic component
in many pharmaceutical agents.
Method:
In this study, cellulose as a heterogeneous support was used to prepare an efficient solid
catalyst. Cellulose, as the most abundant organic polymer, is a suitable material for this purpose.
Then, by immobilizing polyoxomolybdate by a linker on the surface of this carbon-based material,
we succeeded in producing Cell@(CH2)3N=Mo[Mo5O18] nanocatalyst. The structure and properties
of this catalyst were confirmed by various analyses including FT-IR, XRD, EDS-map, FESEM,
and TGA, and its efficacy was evaluated by its use in the preparation of Pyrano[2,3-
d]pyrimidine derivatives through a multicomponent reaction between aryl aldehydes, malononitrile,
and barbituric acid.
Results:
The results of this study showed that this new and non-toxic organo-inorganic hybrid
nanocatalyst provides the desired products in a short time and with appropriate efficiency.
Conclusion:
The key features of the present protocol include reusability of the catalyst, ease of
recovery, ambient reaction conditions, and simple work-up procedure that make it economic and
sustainable.
Publisher
Bentham Science Publishers Ltd.
Subject
Organic Chemistry,Analytical Chemistry,Catalysis
Cited by
1 articles.
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