반응 #1607

ord-0cdfb3a6a39e4aada49cd2cfa61b5f7c

반응 방정식

[Cl-].[NH4+]
ammonium chloride
CCCCCC
hexane
[H-].[Na+]
NaH
O=c1cccc[nH]1
pyridinone
CCC#CCBr
1-bromo-2-pentyne
CCC#CCn1cc(-c2ccc(Cl)cc2)cnc1=O
product
CCC#CCn1cc(-c2ccc(Cl)cc2)cnc1=O
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyrimidinone

용매

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

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

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05726162uspto-grants-1998_03