反応 #1380308

ord-347620f152da4b16bd2c6f0d697eaea6

反応方程式

Sc1nc[nH]n1
3-mercapto-1H-1,2,4-triazole
O=C([O-])[O-].[K+].[K+]
potassium carbonate
OC1CCOc2ccccc21
4-chromanol
O=C(OC(Cl)(Cl)Cl)OC(Cl)(Cl)Cl
triphosgene
c1ccc2c(c1)OCCC2Sc1nc[nH]n1
title compound
収率 47.2%
c1ccc2c(c1)OCCC2Sc1nc[nH]n1
3-(Chroman-4-yl)thio-1H-1,2,4-triazole
収率 47.2%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度with cooling it on an ice bath
  2. 2
    workup.STIRRINGthe reaction mixture was stirred at room temperature for 2 hours
  3. 3
    workup.STIRRINGstirred overnight
  4. 4
    洗浄The reaction solution was washed with water
  5. 5
    濃縮concentrated

実験手順

To a mixture of triphosgene (95 mg) and dichloromethane (4 ml), with stirring, were added pyridine (82 μl) and 4-chromanol (150 mg) in this order with cooling it on an ice bath. Additional pyridine (82 μl) was added, and the reaction mixture was stirred at room temperature for 2 hours. The reaction solution was added to a mixture of 3-mercapto-1H-1,2,4-triazole (110 mg), anhydrous potassium carbonate (200 mg) and N,N-dimethylformamide (2 ml), and stirred overnight. The reaction solution was washed with water, followed by saturated aqueous sodium chloride solution, and concentrated. The residue was subjected to a silica-gel column chromatography with 50% ethyl acetate/hexane to yield the title compound (110 mg).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07238720B2uspto-grants-2007_07