Réaction #2219

ord-3d045ba7bb254c15a155333d94ac21c7

Solvants

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

Mode opératoire

To a suspension of NaH (60% in mineral oil, 700 mg) in dry DMF (100 ml) at 0° C. was added the preceding quinolinone (2.05 g) and the mixture was stirred at 0° C. for one half hour. To the resulting suspension was added 1-bromo-2-pentyne (1.6 g) 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 (1 g).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05728698uspto-grants-1998_03