反応 #5707

ord-3f8581bc16ea4d41a3c766acc9b0ade0

反応方程式

CCCCCC.CCOC(C)=O
hexane ethyl acetate
ClCc1ccc(Cl)cc1
parachlorobenzyl chloride
[H-].[Na+]
sodium hydride
COC(=O)C(NCc1cccc(C(F)(F)F)c1)c1c[nH]c2ccccc12
methyl α-[3-(trifluoromethyl)benzylamino]-indole-3acetate
COC(=O)C(c1cn(Cc2ccc(Cl)cc2)c2ccccc12)N(C)Cc1cccc(C(F)(F)F)c1
title compound
COC(=O)C(c1cn(Cc2ccc(Cl)cc2)c2ccccc12)N(C)Cc1cccc(C(F)(F)F)c1
Methyl α-[N-methyl-3-(trifluoromethyl)benzylamino]-1-(4-chlorobenzyl)indole-3-acetate

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGthe reaction stirred at room temperature for one hour
  2. 2
    洗浄the ether solution was washed two times with water
  3. 3
    抽出The ether extract
  4. 4
    洗浄was then washed with saturated brine
  5. 5
    乾燥dried over anhydrous sodium sulfate
  6. 6
    濃縮concentrated in vacuo
  7. 7
    その他to give the crude product

実験手順

To a magnetically stirred suspension of sodium hydride (60% oil dispersion washed two times with hexane, 80 mg, 2.0 mmol) in 5 mL of dimethylformamide (DMF) under nitrogen was added methyl α-[3-(trifluoromethyl)benzylamino]-indole-3acetate (752 mg, 2.0 mmol) dissolved in 2 mL DMF. Stirring was continued at room temperature for 10 minutes. At the end of this time, 0.322 g (2.0 mmol) of parachlorobenzyl chloride was added and the reaction stirred at room temperature for one hour. The reaction was diluted with ether and the ether solution was washed two times with water. The ether extract was then washed with saturated brine, dried over anhydrous sodium sulfate and concentrated in vacuo to give the crude product. Flash chromatography of the crude product with 100 g of silica gel and using hexane-ethyl acetate (4:10) as the eluent afforded 419 mg of the title compound.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05245046uspto-grants-1993_09