22246-13-5

基本信息
6-氨基-3,4-二氫-1H-喹啉-2-酮
6-氨基-3,4-二氫喹啉-2(1H)-酮
6-氨基-3,4-二氫-2(1H)-喹啉酮
6-amino-3,4-dihydrocarbostyril
6-Amino-3,4-dihydroquinolin-2(1H)
6-AMino-1,3,4-trihydro-quinolin-2-one
6-amino-3,4-dihydro-2(1 )-quinalinone
6-AMINO-3,4-DIHYDRO-2(1H)-QUINOLINONE
6-AMINO-3,4-DIHYDRO-1H-QUINOLIN-2-ONE
6-Amino-3,4-dihydroquinoline-2(1H)-one
6-aMino-3,4-dihydro-2(1H )-quinalinone
2(1H)-Quinolinone, 6-amino-3,4-dihydro-
物理化學(xué)性質(zhì)
制備方法

22246-16-8

22246-13-5
在0℃下,將6-硝基-3,4-二氫喹啉-2(1H)-酮(3g)溶解于甲醇(60mL)中,依次加入鋅粉(5當(dāng)量)和氯化銨(5當(dāng)量)。反應(yīng)混合物在室溫下攪拌1小時,反應(yīng)進(jìn)程通過薄層色譜(TLC)監(jiān)測。反應(yīng)完成后,混合物通過硅藻土床過濾,濾液經(jīng)減壓濃縮。殘余物用含5%甲醇的二氯甲烷溶液溶解,隨后用水洗滌。有機(jī)層用無水硫酸鈉干燥,過濾后減壓濃縮,得到6-氨基-3,4-二氫喹啉-2(1H)-酮(2.3g,收率91%。產(chǎn)物經(jīng)1H NMR(DMSO-d6, 400MHz)表征:δ 9.654(寬單峰,1H),6.53(雙峰,1H),6.378-6.334(多重峰,2H),4.707(寬單峰,2H),2.699(三重峰,2H),2.330(三重峰,2H)。
參考文獻(xiàn):
[1] Patent: WO2015/38417, 2015, A1. Location in patent: Page/Page column 90; 91
[2] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 16, p. 4606 - 4609
[3] Patent: WO2006/71940, 2006, A2. Location in patent: Page/Page column 416
[4] Proceedings of the Imperial Academy (Tokyo), 1939, vol. 15, p. 148,153
[5] Chem. Zentralbl., 1939, vol. 110, # II, p. 3089