Reacción #1244261

Ecuación de reacción

2-nitroimidazole

propargyl bromide

potassium carbonate

DMF

→

10

Rendimiento 85.5%

2-Nitro-1-(prop-2-ynyl)-1H-imidazole

Rendimiento 85.5%

Disolventes

EtOAc

Condiciones de reacción

Tratamiento posterior

1. 1
   Otroreaction
2. 2
   workup.ADDITIONThe reaction was poured onto water (20 mL)
3. 3
   Extracciónextracted into EtOAc (3×20 mL)
4. 4
   LavadoThe combined organics were washed with water (5×20 mL)
5. 5
   ConcentraciónThe organic layer was then concentrated in vacuo
6. 6
   Otropurified on a silica gel cartridge

Procedimiento

To a round bottom flask was added 2-nitroimidazole (500 mg, 4.42 mmol), propargyl bromide (631 mg, 5.31 mmol), potassium carbonate (733 mg, 5.31 mmol) and DMF (5 mL). The reaction was stirred overnight at RT. TLC (EtOAc) indicated complete reaction. The reaction was poured onto water (20 mL) and extracted into EtOAc (3×20 mL). The combined organics were washed with water (5×20 mL). The organic layer was then concentrated in vacuo and purified on a silica gel cartridge using EtOAc:Hex as the eluent to afford 571 mg (85% yield) of 10 as a pale yellow solid. 1H NMR (CDCl3, 400 MHz), δ: 2.63 (1H, d, J=5.6 Hz), 5.23 (2H, d, J=2.4 Hz), 7.20 (1H, d, J=1.2 Hz), 7.46 (1H, s). Mass Spec (lo-res): Calc'd for C6H5N3O2: 151.04; found: 152.10 (M+H).

Fuente