化学合成。
医药
合成路线 1(1. 合成:23504-03-2)
产率:98%
合成条件:With palladium 10% on activated carbon; hydrogen In ethanol at 20℃; for 18 h; Inert atmosphere
实验步骤:将化合物17(3g,9.08mmol)和10%Pd / C(30wt%)在EtOH(48mL)中的混合物在H 2气体下在环境温度下搅拌18小时。 将固体通过硅藻土垫过滤,用MeOH洗涤并减压浓缩。 通过硅胶快速柱色谱法(EtOAc:己烷= 1:1)纯化粗残余物,得到化合物18,为白色结晶固体(1.35g,98%)。 该化合物先前已报道.3mp:87~89。 1H NMR(400MHz,DMSO-d6)δ9.02(s,1H),8.90(s,1H),6.85(d,J = 8.2Hz,1H),6.26(d,J = 2.7Hz,1H),6.16 (dd,J = 8.2,2.3Hz,1H),3.16-2.98(m,1H),1.18-1.04(s,6H); 13C NMR(100MHz,DMSO-d6)δ155.59,154.78,125.87,124.56,105.67,102.11,25.52,22.64。 ESI-MS:m / z = 170(M + H2O)+。
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