55580-08-0
55580-08-0 结构式
基本信息
7-bromo-3,4-dihydro-2h-1-benzoxepin-5-one
7-BROMO-3,4-DIHYDRO-1-BENZOXEPIN-5(2H)-ONE
7-BROMO-3,4-DIHYDROBENZO[B]OXEPIN-5(2H)-ONE
7-BROMO-3,4-DIHYDRO-2H-BENZO[B]OXEPIN-5-ONE
1-Benzoxepin-5(2H)-one, 7-bromo-3,4-dihydro-
JR-8190, 7-Bromo-3,4-dihydrobenzo[b]oxepin-5(2H)-one, 97%
7-Bromo-3,4-dihydrobenzo[b]oxepin-5(2H)-one 7-Bromo-3,4-dihydrobenzo[b]oxepin-5(2H)-one
制备方法
1189816-63-4
55580-08-0
步骤H2: 将1-[5-溴-2-(2-溴乙氧基)苯基]乙酮(9.0g,28.0mmol)溶解于THF(175mL)中,冷却至0℃。在搅拌下,缓慢加入氢化钠(0.805g,33.5mmol)。反应混合物小心加热至回流,并维持回流状态20小时。反应完成后,将混合物冷却至室温,用2M HCl(50mL)淬灭反应。将混合物转移至分液漏斗中,加入盐水(300mL)和EtOAc(250mL)进行萃取。分离有机层,用无水硫酸钠干燥,过滤后减压浓缩。粗产物通过硅胶柱色谱法纯化,洗脱剂为10-30% EtOAc/己烷梯度。收集纯净的级分,减压浓缩,得到7-溴-3,4-二氢-2H-苯并[B]氧杂环庚烷-5-酮(5.41g,22.4mmol,产率80%),为无色油状物。LCMS(M + H)+ = 242.95。1H NMR(500MHz,CDCl3)δ 7.91-7.85(m,1H),7.54-7.48(m,1H),6.98(d,J = 8.5Hz,1H),4.25(t,J = 6.6Hz,2H),2.91(t,J = 6.9Hz,2H),2.23(quin,J = 6.8Hz,2H)。
参考文献:
[1] Patent: WO2012/162330, 2012, A1. Location in patent: Page/Page column 41-42
[2] Patent: US2009/247567, 2009, A1. Location in patent: Page/Page column 183
[3] Patent: US2011/76291, 2011, A1. Location in patent: Page/Page column 144-145
[4] Journal of Medicinal Chemistry, 2017, vol. 60, # 2, p. 627 - 640
