Реакция #1670

ord-3aaa2f0964b0473a962a140eaa35f34c

Уравнение реакции

[Cl-].[NH4+]
ammonium chloride
[H-].[Na+]
NaH
O=c1cccc[nH]1
pyridinone
CCCCCC.CCOC(C)=O
hexane ethyl acetate
CCC#CCBr
1-bromo-2-pentyne
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone

Растворители

Условия реакции

Температура
0°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.WAITThe resulting mixture was kept at 0° C. during one half hour
  2. 2
    ЭкстракцияThe aqueous suspension was extracted with ether (3×100 ml)
  3. 3
    Промывкаthe combined ether layers washed with brine
  4. 4
    Другоеdried
  5. 5
    Другоеyielding the crude product

Методика

To a suspension of NaH (60% in mineral oil, 200 mg) in dry DMF (50 ml) at 0° C. was added the preceding pyridinone and the mixture was stirred at 0° C. for one half hour. To the resulting suspension was added 1-bromo-2-pentyne dropwise. The resulting mixture was kept at 0° C. during one half hour and poured into saturated aqueous ammonium chloride (200 ml). The aqueous suspension was extracted with ether (3×100 ml) and the combined ether layers washed with brine and dried, yielding the crude product. After column chromatography (silica gel, hexane:ethyl acetate 8:2) the product was obtained as a white amorphous solid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05726176uspto-grants-1998_03