Reacción #2298641
ord-a60e2284ddd343c7998f755014dbc362
Ecuación de reacción
4-[2-[2-ethyl-4-methyl-6-oxo-1,6dihydro-1-pyrimidinyl]ethoxy]benzyl hydroxylamine
KOCN
→
compound
Rendimiento 85.2%
N-[4-[2-[2-Ethyl-4-methyl-6-oxo-1,6-dihydro-1-pyrimidinyl]ethoxy]benzyl]N-hydroxyurea
Rendimiento 85.2%
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Temperatura
30°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Extracciónextracted with ethyl acetate (3×10 ml)
- 2LavadoThe combined organic layers were washed with brine
- 3Secadodried over anhydrous Na2SO4
- 4Concentraciónconcentrated
Procedimiento
To a stirred solution of 4-[2-[2-ethyl-4-methyl-6-oxo-1,6dihydro-1-pyrimidinyl]ethoxy]benzyl hydroxylamine (303 mg, 1.0 mmol) (obtained from preparation 18) in a mixture of water (2 ml) and acetic acid (0.5 ml) was added a solution of KOCN (343 mg, 3.0 mmol) in water (1 ml) and stirred for 1 h at 30° C. The reaction mixture was diluted with water and extracted with ethyl acetate (3×10 ml). The combined organic layers were washed with brine, dried over anhydrous Na2SO4 and concentrated to yield the compound (295 mg, 85%).