摘要
We have described a convenient regioselective one-pot approach to pyrazolo5b;1,5-a5d;- and imidazo5b;1,2-a5d;pyrimidine derivatives from α,β-unsaturated imines generated in situ and amino heterocycles. Reaction is general with respect to all three components, namely (i) nitrile, (ii) aldehyde, and (iii) amino heterocycle reagents. Good yields (52–77%), convenient isolation of the targeted molecules are the distinct characteristics of the developed protocol.