HRID2203033

反应详情

EQUATION

反应方程式

HRID 2203033 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
60 °C

PROCEDURE

实验过程

To a mixture of 4-hydroxy-1-(2-((1RS,2SR)-2-(2-hydroxypropan-2-yl)cyclopropyl)-1-methyl-1H-benzimidazol-6-yl)pyridin-2(1H)-one (100 mg), (4-fluorophenyl)methanol (74.3 mg), tributylphosphine (0.219 ml) and THF (10 ml) was added 1,1′-(azodicarbonyl)dipiperidine (223 mg), and the mixture was stirred at 60° C. for 2 h. The reaction mixture was diluted with EtOAc, washed with water and brine successively, dried over MgSO4, filtered through NH silica gel pad, and concentrated in vacuo. The residue was purified by column chromatography (hexane/EtOAc then EtOAc/MeOH). The resulting solid was washed with toluene, and recrystallized from IPA-IPE to give the title compound (49.6 mg) as an off-white solid.

WORKUP

后处理

  1. washwashed with water and brine successively
  2. dry with materialdried over MgSO4
  3. filtrationfiltered through NH silica gel pad
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by column chromatography (hexane/EtOAc
  6. washThe resulting solid was washed with toluene
  7. customrecrystallized from IPA-IPE