A tandem copper (II)-promoted synthesis of 2-substituted pyrrolo[2,1-f][1,2,4] triazin-4(3H)-ones
Tetrahedron(2013)
Abstract
An efficient tandem method for the annulation of 1-amino-1H-pyrrole-2-amides with various substituted benzaldehydes, heteroaryl aldehydes, alkyl aldehydes or even acetals, promoted by cupric chloride, to synthesize 2-substituted pyrrolo[2,1-f][1,2,4]triazin-4(3H)-ones is reported. This approach provides a useful method for constructing the privileged structure in medicinal chemistry. Electron-donating groups on both partners could accelerate the reaction.
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Key words
Tandem annulation,Cupric chloride,1-Amino-1H-pyrrole-2-amides,Privileged structure,Pyrrolo[2,1-f][1,2,4]triazin-4(3H)-ones
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