2,4-二氯噻吩并[3,2-d]嘧啶主要作为医药中间体或农药中间体,用于相关药物和农药的合成制备。
医药; 农药
合成路线 1(1. 合成:16234-14-3)
产率:100%
合成条件:for 2 h; Heating / reflux
实验步骤:向尿嘧啶(5g,29mmol)在POCl 3(40mL)中的悬浮液中加入二异丙基乙胺(13mL,74mmol)并将反应物加热回流2小时。 然后通过减压蒸馏除去过量的POCb和二异丙基乙胺,将得到的棕色固体溶解在氯仿中并用水分配。 通过加入5M NaOH使水相呈碱性,再用氯仿萃取两次。 将合并的有机级分用水和盐水洗涤,干燥(Na 2 SO 4),过滤并浓缩,得到产物,为浅棕色固体(6.05g,定量收率)。 1 H NMR(CDCl 3,300MHz):8.16(d,J = 5.4Hz,1H),7.56(d,J = 5.7Hz,1H); LRMS(ESI):m / z计算值[M + H] + 204.94,206.94,实测值205.1,207.0。
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