پديدآورندگان :
Amini Fatemeh Firoozabad Branch, Islamic Azad University , Rezaei Ramin rezaieramin@yahoo.com Firoozabad Branch, Islamic Azad University
چكيده فارسي :
Pyrimidines have occupied an important place in organic and medicinal chemistry, mainly
due to their diverse therapeutic and pharmacologicalproperties [1]. Among them, fused
pyrimidines have been used as a common source for the synthesis of new therapeutic agents.
Recent studies have shown that pyrimidine-fused heterocycles, particularly their oxo and
thioxo derivatives, possess a wide range of biological activity and for this reason, they are
extensively used in the design of new drugs [2].The synthesis of pyrimidine derivatives by a
multicomponent reaction (MCR) is an attractive approach for the construction of this class of
compounds [3]. It has been proven recently that this is a mild, worthwhile catalyst, which is
efficiently and selectively catalyzes various organic transformations and synthesis. The
catalyst was recovered activated and reused for two consecutive times with only slight
variation in the yields of the products. Now, we report an efficient and convenient procedure
for the One-Pot synthesis of aromatic aldehyde, barbituric acid and aromatic amine, by using
homogeneous catalyst cyclohexane-1,4-diyl bis(hydrogen sulfate) [CDBH]to produce the
pyrimidine-fused heterocycle derivatives in excellent yields (Figure 1).