反应 #80613

ord-c5330df2d83d4e779a010d9b0a5e81f0

反应条件

温度
0°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他ice bath was removed
  2. 2
    workup.STIRRINGsolution stirred for 1 hour
  3. 3
    workup.STIRRINGAfter stirring for 2 hours
  4. 4
    温度the reaction was heated
  5. 5
    温度to reflux for 48 hours
  6. 6
    温度The reaction mixture was cooled to room temperature
  7. 7
    workup.STIRRINGAfter stirring for 5 minutes
  8. 8
    workup.STIRRINGthe mixture stirred for 20 hours
  9. 9
    萃取extracted with ether (2×250).The ethereal layer
  10. 10
    干燥was dried over sodium sulfate
  11. 11
    过滤filtered
  12. 12
    浓缩concentrated in vacuo
  13. 13
    其他The crude solid (568 mg) was chromatographed [silica gel, ethyl acetate/toluene (3/7)]

实验过程

To a clear solution of 2-(4-chlorophenyl)-1-[4-(methylsulfonyl)phenyl]-4-(trifluoromethyl)-1H-imidazole from Example 2 (400 mg, 1 mmol) in tetrahydrofuran (THF) (8 mL) at 0° C., n-BuMgCl (2M solution in THF, 2 mL, 4 mmol) was added over 10 minutes. After stirring for additional 10 minutes, ice bath was removed and solution stirred for 1 hour. The reaction mixture was re-cooled to 0° C. and triethylborane (1M solution in THF, 5 mL, 5 mmol) was added. After stirring for 2 hours, the reaction was heated to reflux for 48 hours. The reaction mixture was cooled to room temperature and treated with aqueous sodium acetate (1 g in 4 mL water). After stirring for 5 minutes, solid hydroxylamine-O-sulfonic acid (1 g) was added and the mixture stirred for 20 hours. The reaction mixture was diluted with water and extracted with ether (2×250).The ethereal layer was dried over sodium sulfate, filtered and concentrated in vacuo. The crude solid (568 mg) was chromatographed [silica gel, ethyl acetate/toluene (3/7)] to give 4-[2-(4-chlorophenyl)-4-(trifluoromethyl)-1H-imidazol-1-yl]benzenesulfonamide (260 mg, 65%): mp (DSC) 225° C.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05616601uspto-grants-1997_04