路线1:以化合物59为原料合成4-氯-7-甲氧基-1,6-萘啶
- 步骤:将化合物59(332mg,1.89mmol)溶解在20mL乙腈中,加入DIEA(653μL,3.95mmol),搅拌下滴加磷酰氯(345μl,3.78mmol);反应液在70℃搅拌30分钟后冷却至室温,倒入冰水中,用2N NaOH调节至pH8,用EA萃取,饱和NH₄Cl溶液洗涤,无水Na₂SO₄干燥,减压浓缩,残余物经柱色谱纯化得到标题化合物。
- 条件:N-乙基-N,N-二异丙基胺、磷酰氯为试剂,乙腈为溶剂,70℃反应0.5小时。
- 产率:92%
- 参考文献:
- [1] Patent: US2018/244667, 2018, A1. Location in patent: Paragraph 0110
- [2] Patent: WO2008/8539, 2008, A2. Location in patent: Page/Page column 135
- [3] Patent: US2014/336182, 2014, A1. Location in patent: Paragraph 0312
- [4] Patent: WO2008/124083, 2008, A2. Location in patent: Page/Page column 48
- [5] Patent: WO2007/113565, 2007, A1. Location in patent: Page/Page column 99-100