Reacción #1675

Ecuación de reacción

ammonium chloride

hexane

NaH

pyridinone

1-bromo-2-pentyne

→

product

5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyrimidinone

Disolventes

DMF

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.WAITThe resulting mixture was kept at 0° C. for one half hour
2. 2
   ExtracciónThe aqueous suspension was extracted with ether (3×100 ml)
3. 3
   Lavadothe combined ether layers washed with brine
4. 4
   Otrodried
5. 5
   Otroyielding the crude product

Procedimiento

To a suspension of NaH (60% in mineral oil, 340 mg) in dry DMF (75 ml) at 0° C. was added the preceding pyridinone (1.0 g) and the mixture was stirred at 0° C. for one half hour. To the resulting suspension was added 1-bromo-2-pentyne (750 mg) dropwise. The resulting mixture was kept at 0° C. for one half hour and poured into saturated aqueous ammonium chloride (200 ml). The aqueous suspension was extracted with ether (3×100 ml), the combined ether layers washed with brine and dried, yielding the crude product. Trituration with hexane yielded the product as a yellow solid.

Fuente