1185428-32-3

基本信息
2-broMo-5h-pyrrolo[2,3-b]pyrazine-7-carbaldehyde
2-BroMo-5H-pyrrolo[2,3-b]pyrazine-7-carboxaldehyde
5H-Pyrrolo[2,3-b]pyrazine-7-carboxaldehyde, 2-bromo-
制备方法
![(2-BROMO-5H-PYRROLO[2,3-B]PYRAZIN-7-YL)METHANOL](/CAS/GIF/1334674-88-2.gif)
1334674-88-2
![2-溴-5H-吡咯并[2,3-B]吡嗪-7-甲醛](/CAS/20150408/GIF/1185428-32-3.gif)
1185428-32-3
步骤3. 2-溴-5H-吡咯并[2,3-b]吡嗪-7-甲醛的合成。 在2-溴-5H-吡咯并[2,3-b]吡嗪-7-基甲醇(127g,562mmol)的丙酮(2.5L)悬浮液中,缓慢滴加Jones试剂(253mL,674mmol)。滴加完毕后,将反应混合物于室温下搅拌50分钟,观察到悬浮液逐渐澄清并析出棕色固体。Jones试剂(2.67M)的制备需在低于10℃的条件下,将浓H2SO4(184mL)小心加入CrO3(213.6g)中,随后用H2O稀释至800mL。反应完成后,用异丙醇(60mL)淬灭反应,过滤分离固体。滤饼用丙酮(1L×2)洗涤,合并滤液并浓缩,得到目标产物2-溴-5H-吡咯并[2,3-b]吡嗪-7-甲醛(320g,收率84.4%),为黄色固体。
参考文献:
[1] Journal of Medicinal Chemistry, 2013, vol. 56, # 1, p. 345 - 356
[2] Patent: US2015/158864, 2015, A1. Location in patent: Paragraph 0650
[3] Patent: WO2016/178110, 2016, A1. Location in patent: Page/Page column 30
[4] Patent: US2011/230462, 2011, A1. Location in patent: Page/Page column 54; 56
[5] Patent: WO2011/144584, 2011, A1. Location in patent: Page/Page column 37