Reaktion #10401

ord-2215a032e5f9454f83cc5b8245d8b56f

Reaktionsgleichung

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
Ausbeute 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
Ausbeute 63.1%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed with saturated NaHCO3, water, and brine
  2. 2
    TrocknenThe organic layer is dried over MgSO4
  3. 3
    Filtrationfiltered
  4. 4
    EinengenThe filtrate is concentrated under vacuum
  5. 5
    Sonstigepurified via flash column chromatography (1:2 ethyl acetate/hexanes)

Vorschrift

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+).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07094780B1uspto-grants-2006_08