反応 #52227

ord-ab5cf9bb3daa461ab50b0a25299f6c60

反応方程式

O=C([O-])O
bicarbonate
COc1cc(N(CC(OC)OC)S(C)(=O)=O)ccc1F
N-(2,2-dimethoxyethyl)-N-methanesulphonyl-4-fluoro-3-methoxyaniline
COc1cc2c(ccn2S(C)(=O)=O)cc1F
5-fluoro-1-methanesulphonyl-6-methoxyindole

反応条件

温度
70°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度cooled
  2. 2
    workup.ADDITIONpoured onto ice/
  3. 3
    その他The organic layer was separated
  4. 4
    洗浄washed with sat. sod
  5. 5
    乾燥The solution was dried (MgSO4)
  6. 6
    その他evaporated in vacuo

実験手順

To a solution of N-(2,2-dimethoxyethyl)-N-methanesulphonyl-4-fluoro-3-methoxyaniline (1.91 g, 0.65 mmol) in dry toluene at 0° C. under argon, was added slowly a solution of TiCl4 (0.173 g, 0.911 mmol) in dry toluene (10 ml). The solution was then heated to 70° C. for 1 h. cooled and poured onto ice/sat. sod. bicarbonate solution (20 ml). The organic layer was separated, washed with sat. sod. bicarbonate solution, 0.5% hydrochloric acid (2×20 ml) and water (2×20 ml). The solution was dried (MgSO4) and evaporated in vacuo to give 5-fluoro-1-methanesulphonyl-6-methoxyindole ((0.102 g)

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06855715B1uspto-grants-2005_02