Reacción #1785949

Ecuación de reacción

(±)-2-oxo-3-tert-butoxycarbonylamino-5-cyclohexyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine

bromomethyl tert-butyl ketone

potassium carbonate

potassium iodide

→

(±)-1-tert-butylcarbonylmethyl-2-oxo-3-tert-butoxycarbonylamino-5-cyclohexyl-1,3,4,5-tetrahydro-2H -1,5-benzodiazepine

Disolventes

dimethyl sulfoxide

Condiciones de reacción

Tratamiento posterior

1. 1
   Extracciónfollowed by extraction with ethyl acetate
2. 2
   LavadoThe organic layer was washed with brine
3. 3
   Secadodried over an hydrous sodium sulfate
4. 4
   OtroThe solvent was evaporated under reduced pressure
5. 5
   Otrothe residue was purified by silica gel colomn chromatography (ethyl acetate: n-hexane=1:3), whereby the title compound (2.3 g)
6. 6
   Otrowas obtained

Procedimiento

To a solution of (±)-2-oxo-3-tert-butoxycarbonylamino-5-cyclohexyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine (3.35 g) in dimethyl sulfoxide (30 mL), bromomethyl tert-butyl ketone (2 g), potassium carbonate (1.55 g), potassium iodide (125mg) and tetra (n-butyl) ammonium bromide (120mg) were added, followed by stirring at room temperature for 1 hour. The reaction mixture was poured into ice water, followed by extraction with ethyl acetate. The organic layer was washed with brine and then dried over an hydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel colomn chromatography (ethyl acetate: n-hexane=1:3), whereby the title compound (2.3 g) was obtained.

Fuente