Reacción #434875

ord-05f1036f33e3430cb005bf0bdcaaff02

Ecuación de reacción

CC(=O)[O-].O.O.O.[Na+]
sodium acetate trihydrate
O=C(C(Br)Br)C(F)(F)F
1,1-dibromo-3,3,3-trifluoroacetone
[Na+].[OH-]
NaOH
N=C(N)NN.O=C(O)O
aminoguanidine bicarbonate
Nc1nncc(C(F)(F)F)n1
mixture
Rendimiento 53.1%
Nc1nncc(C(F)(F)F)n1
3-Amino-5-trifluoromethyl-1,2,4-triazine
Rendimiento 53.1%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe solution was heated
  2. 2
    Temperaturaat reflux under nitrogen for 30 min
  3. 3
    FiltraciónThe solid was collected by filtration
  4. 4
    Lavadowashed with water
  5. 5
    Otrodried at 60° C. under vacuum

Procedimiento

To a stirred solution of sodium acetate trihydrate (22.62 g, 166.2 mmol) in water (80 ml) was added 1,1-dibromo-3,3,3-trifluoroacetone (21.57 g, 79.9 mmol). The solution was heated at reflux under nitrogen for 30 min, then allowed to cool to room temperature before adding solid aminoguanidine bicarbonate (10.88 g, 79.9 mmol). The resulting pale yellow solution (pH 5) was stirred at room temperature for 3 h, then 4 N aqueous NaOH solution (40 ml, 160 mmol) was added causing a precipitate to appear. The mixture (pH 10) was stirred under nitrogen for a further 39 h. The solid was collected by filtration, washed with water and dried at 60° C. under vacuum to give 6.96 g of a mixture of two isomers in a 28:72 ratio. This was further purified by flash chromatography (silica gel, 30% EtOAc/isohexane), then recrystallised from ethanol to afford 3.53 g (27%) of the title compound: 1H NMR (400 MHz, DMSO-d6) δ 8.00 (2H, br s), 9.08 (1H, s).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07176203B2uspto-grants-2007_02