1427158-05-1Relevant articles and documents
A tandem copper (II)-promoted synthesis of 2-substituted pyrrolo[2,1-f][1,2,4] triazin-4(3H)-ones
Chen, Yanhong,Xiang, Haoyue,Tan, Cun,Xie, Yuyuan,Yang, Chunhao
, p. 2714 - 2719 (2013/03/28)
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.