作者:Adriana Chilin、Giovanni Marzaro、Samuele Zanatta、Vera Barbieri、Giovanni Pastorini、Paolo Manzini、Adriano Guiotto
DOI:10.1016/j.tet.2006.09.103
日期:2006.12
A new synthetic pathway to quinazolines is described. This new method uses hexamethylenetetramine in TFA and potassium ferricyanide in aqueous ethanolic KOH, starting from simple N-protected anilines. The method affords substituted quinazolines with high selectivities and good yields, reducing reaction-time and work-up operations.
描述了一种合成喹唑啉的新途径。该新方法从简单的N保护苯胺开始,在TFA中使用六亚甲基四胺,在含水乙醇KOH中使用铁氰化钾。该方法提供了具有高选择性和良好收率的取代的喹唑啉,减少了反应时间和后处理操作。