反応 #10400

ord-eeeb0d9ca8654a97b94c5952a45d29e4

反応方程式

O=C(O)c1cc(F)c(F)cc1Nc1ccc(F)cc1F
2-(2,4-difluoroanilino)-4,5-difluorobenzoic acid
CC(C)(C)OC(=O)NN
tert-butyl carbazate
CCN=C=NCCCN(C)C
1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide
CC(C)(C)OC(=O)N(N)C(=O)c1cc(F)c(F)cc1Nc1ccc(F)cc1F
[2-(2,4-difluoroanilino)-4,5-difluorobenzoyl]-hydrazinecarboxylic acid tert-butyl ester
収率 72.5%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    洗浄washed with saturated NaHCO3, water, and brine
  2. 2
    乾燥The organic layer is dried over Na2SO4
  3. 3
    濃縮concentrated under vacuum
  4. 4
    その他purified via column chromatography (1:3 ethyl acetate/hexanes)

実験手順

To a solution of 2-(2,4-difluoroanilino)-4,5-difluorobenzoic acid (Example 5, 2.18 g, 7.6 mmol) and tert-butyl carbazate (1.57 g, 11.8 mmol) in dichloromethane (30 mL) is added 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (2.25 g, 11.77 mmol). After stirring for 16 hours at room temperature, the reaction mixture is diluted with dichloromethane and then washed with saturated NaHCO3, water, and brine. The organic layer is dried over Na2SO4, concentrated under vacuum, and purified via column chromatography (1:3 ethyl acetate/hexanes) to afford [2-(2,4-difluoroanilino)-4,5-difluorobenzoyl]-hydrazinecarboxylic acid tert-butyl ester as a solid (2.20 g). MS EI: m/z 400 (M+).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07094780B1uspto-grants-2006_08