反応 #5838

ord-57a90189c8764512903a44bb9d37a3a5

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    洗浄the ethyl acetate layer was sequentially washed with water
  2. 2
    乾燥a saturated sodium chloride aqueous solution twice in each case, and dried over magnesium sulfate
  3. 3
    ろ過The solution was filtered
  4. 4
    その他evaporated under a reduced pressure
  5. 5
    その他resulting residue
  6. 6
    その他was purified on a silica gel column (silica gel 50 g, eluant: 5% methanol in chloroform)

実験手順

1.31 g of the product of Example 172 was dissolved in 3 ml of dimethylformamide, to the solution were added 644 mg of 1,2-dibromoethane and 1.13 g of anhydrous potassium carbonate at a room temperature, and the mixture was stirred for 24 hours. After adding 100 ml of ethyl acetate, the ethyl acetate layer was sequentially washed with water and a saturated sodium chloride aqueous solution twice in each case, and dried over magnesium sulfate. The solution was filtered and evaporated under a reduced pressure, and resulting residue was purified on a silica gel column (silica gel 50 g, eluant: 5% methanol in chloroform), to obtain 356 mg of the title compound in a colorless amorphous form, while recovering the residual starting material.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05245034uspto-grants-1993_09