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4.2 5-甲氧基喹啉的合成 (1)在氬氣保護(hù)下,將5-羥基喹啉(4.0 g,27.6 mmol)溶解于無水DMF(60 mL)中,冷卻至0℃。隨后緩慢加入NaH(1.33 g,33.12 mmol,60%礦物油分散體)。保持0℃下攪拌反應(yīng)混合物30分鐘。然后,向懸浮液中滴加甲基碘(4.7 g,33.12 mmol),并讓反應(yīng)混合物逐漸升溫至室溫,繼續(xù)攪拌30分鐘。反應(yīng)完成后,用300 mL水淬滅反應(yīng),然后用乙醚(6×100 mL)進(jìn)行萃取。合并有機(jī)層,依次用水和鹽水洗滌,用無水Na2SO4干燥,過濾后減壓濃縮溶劑,得到棕色油狀目標(biāo)產(chǎn)物5-甲氧基喹啉。產(chǎn)量:4.03 g(92%)。 1H NMR (400 MHz, CDCl3) δ 8.95 (dd, J = 4.2, 2.0 Hz, 1H), 8.62 (dd, J = 8.4, 1.2 Hz, 1H), 7.74 (d, J = 8.0 Hz, 1H), 7.65 (t, J = 8.4 Hz, 1H), 7.42 (dd, J = 8.4, 4.4 Hz, 1H), 6.90 (d, J = 8.0 Hz, 1H), 4.05 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 155.17, 150.66, 148.70, 130.81, 129.37, 121.58, 120.85, 120.19, 104.22, 55.76.
參考文獻(xiàn):
[1] European Journal of Medicinal Chemistry, 2015, vol. 101, p. 754 - 768
[2] Patent: KR101778938, 2017, B1. Location in patent: Paragraph 0147-0148; 0155; 0164-0166
[3] Dissertation , S. 23,
[4] Chemische Berichte, 1882, vol. 15, p. 1979
[5] Chemische Berichte, 1887, vol. 20, p. 731