Reacción #7313

ord-7ed350118fc746a58b79ffe1365ea045

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe reaction mixture is subsequently concentrated by evaporation in a vacuum
  2. 2
    workup.DISSOLUTIONdissolved again in ethyl acetate
  3. 3
    Lavadowashed with water and saturated sodium chloride solution
  4. 4
    OtroThe organic phase is separated
  5. 5
    Secadodried with magnesium sulphate
  6. 6
    Concentraciónconcentrated by evaporation

Procedimiento

240 mg of 1-(5-chlorobenzotriazol-1-yl)-propan-2-one are dissolved in 4 ml of a 2-molar solution of ammonia in ethanol, then 64 mg of sodium cyanide and 91 mg of ammonium chloride are added and the mixture is stirred over night at room temperature. The reaction mixture is subsequently concentrated by evaporation in a vacuum, dissolved again in ethyl acetate, and washed with water and saturated sodium chloride solution. The organic phase is separated, dried with magnesium sulphate and concentrated by evaporation. 2-amino-3-(5-chlorobenzotriazol-1-yl)-2-methylpropionitrile is thus obtained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07084280B2uspto-grants-2006_08