HRID1910684

反应详情

EQUATION

反应方程式

HRID 1910684 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

5,7-Dichloro-3-(2-chlorophenethyl)-1-(4-methoxybenzyl)-1H-benzo[e][1,4]diazepin-2(3H)-one (245 mg) and di-tert-butyl 2-oxo-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-imidazo[4,5-b]pyridine-1,3(2H)-dicarboxylate (255 mg, 1.1 eq) were dissolved in dioxane/water (2 mL:0.65 mL), and cesium carbonate (327 mg, 2 eq) was added followed by lithium chloride (64 mg, 3 eq). The mixture was degassed with nitrogen and then tetrakis-triphenylphosphine palladium (0) (58 mg, 0.1 eq) was added. The mixture was degassed again, and the reaction was then heated to 80° C. for three hours. The crude mixture was partitioned between water and EtOAc and the organic fraction was then washed with brine, then dried over sodium sulfate and concentrated onto silica gel and purified by chromatography (gradient: 9:1 hexanes:EtOAc to EtOAc) delivering both the product 90 mg, 23% yield). MS (ES+) m/z 707.9 (M+Na) and m/z 807.9 (M+Na+Boc) and doubly Boc-protected material.

WORKUP

后处理

  1. customThe mixture was degassed with nitrogen
  2. customThe mixture was degassed again
  3. customThe crude mixture was partitioned between water and EtOAc
  4. washthe organic fraction was then washed with brine
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated onto silica gel
  7. custompurified by chromatography (gradient: 9:1 hexanes:EtOAc to EtOAc)