26956-43-4

基本信息
4,5-二氢-4-氧代呋喃[3,2]吡啶
呋喃并[3,2-C]吡啶-4(5H)-酮
4,5-二氢-4-氧代呋喃[3,2]吡啶 1G
Furo[3,2-c]pyridin-4-ol
5H-Furo[3,2-c]pyridin-4-one
FURO[3,2-C]PYRIDIN-4(5H)-ONE
4H,5H-furo[3,2-c]pyridin-4-one
4,5-Dihyro-4-Oxofuro[3,2]Pyridine
4,5-DIHYDRO-4-OXOFURO[3,2-C]PYRIDINE
4-OXO-4,5-DIHYDROFURO[3,2-C]PYRIDINE
4,5-DIHYDRO-4-OXOFURO[3,2-C]PYRIDINE ISO 9001:2015 REACH
物理化学性质
制备方法

119924-26-4
![4,5-二氢-4-氧代呋喃[3,2]吡啶](/CAS/GIF/26956-43-4.gif)
26956-43-4
以(E)-3-(呋喃-2-基)丙烯酰叠氮化物为原料合成4,5-二氢-4-氧代呋喃[3,2]吡啶的一般步骤如下:将(E)-3-(呋喃-2-基)丙烯酰叠氮化物(150 g,920 mmol)加入预热至100℃的甲苯(800 mL)中,搅拌反应混合物30分钟。反应完成后,减压蒸馏去除溶剂。将残余物溶解于邻二氯苯(800 mL)中,加入碘(1 g)作为催化剂。将反应混合物在180℃下搅拌2小时,随后减压蒸发去除溶剂。将残余物溶解于甲醇中,过滤收集沉淀物,滤液经减压浓缩。最后,用二异丙醚洗涤残余物,得到目标产物4,5-二氢-4-氧代呋喃[3,2]吡啶(100 g,产率80%)。产物经1H-NMR(DMSO-d6)表征:δ 6.85(1H,dd,J = 7.1, 1.0 Hz),6.92(1H,dd,J = 1.9, 1.0 Hz),7.29(1H,d,J = 7.1 Hz),7.86(1H,d,J = 1.9 Hz),11.42(1H,brs)。
参考文献:
[1] Patent: EP2100895, 2009, A1. Location in patent: Page/Page column 44
[2] Patent: WO2013/163244, 2013, A1. Location in patent: Paragraph 00273
[3] Patent: WO2016/37578, 2016, A1. Location in patent: Page/Page column 146
[4] Patent: WO2004/100947, 2004, A2. Location in patent: Page 20-21; 16
[5] Patent: WO2005/67900, 2005, A2. Location in patent: Page/Page column 39-40