HRID1019715

反应详情

EQUATION

反应方程式

HRID 1019715 的结构方程式

CONDITIONS

反应条件

温度
90 °C

PROCEDURE

实验过程

A scintillation vial equipped with a stirbar was charged with (S)-6-bromo-1-(1-phenylethyl)-1H-imidazo[4,5-b]pyrazin-2-ol (1.0 equiv), (Z)-prop-1-enyl boronic acid (2.0 equiv) and (DPPF)PdCl2 (0.10 equiv). The vial was fitted with a septum-lined cap and purged with nitrogen for 5-10 min. To this mixture was added dioxane (16.6 volume equivalents) and degassed 2N K2CO3 (4.2 volume equivalents) by syringe. The resulting mixture was heated to 90° C. overnight. The mixture was cooled to room temperature, diluted with EtOAc, washed with twice with saturated aq. NaHCO3, and once with brine. The organic layer was dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Biotage MPLC 5%-40% EtOAc/Hexanes) provided the title compound (63%) as an off-white foam. LCMS m/z (APCI)=281.1 (M+H).

WORKUP

后处理

  1. customA scintillation vial equipped with a stirbar
  2. customThe vial was fitted with a septum-lined
  3. customcap
  4. custompurged with nitrogen for 5-10 min
  5. additionTo this mixture was added dioxane (16.6 volume equivalents)
  6. customdegassed 2N K2CO3 (4.2 volume equivalents) by syringe
  7. temperatureThe mixture was cooled to room temperature
  8. additiondiluted with EtOAc
  9. washwashed with twice with saturated aq. NaHCO3
  10. dry with materialThe organic layer was dried over sodium sulfate
  11. filtrationfiltered
  12. concentrationconcentrated in vacuo