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23833-99-0
4-氯-8-硝基喹啉(6a)的合成步驟如下:將4-氯喹啉(10.0g,61.3mmol)緩慢加入硫酸(45mL)中,反應(yīng)過(guò)程中需控制溫度不超過(guò)15℃。隨后,將反應(yīng)液冷卻至-15℃,并在該溫度下逐滴加入發(fā)煙硝酸。加畢,將反應(yīng)混合物逐漸升溫至室溫,并繼續(xù)攪拌3小時(shí)。反應(yīng)完成后,將混合物傾倒在冰上,用NH4OH調(diào)節(jié)pH至9,過(guò)濾收集析出的固體沉淀,用水充分洗滌,干燥后以甲醇重結(jié)晶,得到目標(biāo)產(chǎn)物4-氯-8-硝基喹啉(6a)7.5g,產(chǎn)率59%。產(chǎn)物表征數(shù)據(jù)如下:熔點(diǎn)128-129℃(文獻(xiàn)值129-130℃);1H NMR (CDCl3) δ 7.67 (d, 1H, J=4.5Hz), 7.75 (dd, 1H, J=8.6Hz, J=7.6Hz), 8.10 (dd, 1H, J=7.6Hz, J=1.3Hz), 8.48 (dd, 1H, J=8.6Hz, J=1.3Hz), 8.94 (d, 1H, J=4.5Hz);13C NMR (CDCl3) δ 123.0, 124.4, 126.5, 127.5, 128.3, 140.6, 143.2, 148.7, 152.1。
參考文獻(xiàn):
[1] Chemical and Pharmaceutical Bulletin, 2013, vol. 61, # 7, p. 747 - 756
[2] Patent: WO2004/14906, 2004, A2. Location in patent: Page 19
[3] Bioorganic and Medicinal Chemistry Letters, 2009, vol. 19, # 13, p. 3517 - 3520
[4] Journal of Enzyme Inhibition and Medicinal Chemistry, 2015, vol. 30, # 4, p. 607 - 614
[5] Patent: US2010/249182, 2010, A1. Location in patent: Page/Page column 3; 5