反応 #10401

ord-2215a032e5f9454f83cc5b8245d8b56f

反応方程式

O=C(O)c1cc(F)c(F)c(Cl)c1NC1CC1
3-chloro-2-cyclopropylamino-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)c(Cl)c1NC1CC1
title compound
収率 63.1%
CC(C)(C)OC(=O)N(N)C(=O)c1cc(F)c(F)c(Cl)c1NC1CC1
(3-Chloro-2-cyclopropylamino-4,5-difluorobenzoyl)-hydrazinecarboxylic acid tert-butyl ester
収率 63.1%

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 MgSO4
  3. 3
    ろ過filtered
  4. 4
    濃縮The filtrate is concentrated under vacuum
  5. 5
    その他purified via flash column chromatography (1:2 ethyl acetate/hexanes)

実験手順

To a solution of 3-chloro-2-cyclopropylamino-4,5-difluorobenzoic acid (Example 5d, 2.09 g, 8.45 mmol) in dichloromethane (30 mL) is added tert-butyl carbazate (1.67 g, 12.7 mmol) and 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (2.43 g, 12.7 mmol). After 16 hours, the reaction mixture is diluted with dichloromethane and washed with saturated NaHCO3, water, and brine. The organic layer is dried over MgSO4 and filtered. The filtrate is concentrated under vacuum and purified via flash column chromatography (1:2 ethyl acetate/hexanes) to afford the title compound (1.93 g). MS EI: m/z 360 (M+).

出典

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