Allyl bromide → HCID 9967065, 화합물

HRID 2215312노트

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HRID 2215312 반응식
[H-].[Na+].[CH2:3](Br)[CH:4]=[CH2:5].[Cl:7][C:8]1[CH:9]=[C:10]([CH:21]=[C:22]([Cl:24])[CH:23]=1)[O:11][C:12]1[C:13]([CH2:19][CH3:20])=[N:14][NH:15][C:16]=1[CH2:17][CH3:18]>CN(C)C=O>[CH2:3]([N:14]1[C:13]([CH2:19][CH3:20])=[C:12]([O:11][C:10]2[CH:21]=[C:22]([Cl:24])[CH:23]=[C:8]([Cl:7])[CH:9]=2)[C:16]([CH2:17][CH3:18])=[N:15]1)[CH:4]=[CH2:5]

참가 물질

5

실험 절차

Sodium hydride (60% dispersion in oil, 770 mg, 19.2 mmol) was added to a stirred solution of allyl bromide (1.70 ml, 19.2 mmol) and the pyrazole of Example 3 (5.00 g, 17.5 mmol) in N,N-dimethylformamide (20 ml) at 0° C. under nitrogen. The reaction was warmed to room temperature and stirred for 1 hour. The reaction mixture was quenched by the addition of water (100 ml) and the aqueous phase was extracted with ether (2×50 ml). The combined organic phases were washed with water (30 ml) and brine (30 ml), dried over magnesium sulphate, filtered and concentrated under reduced pressure to leave a brown oil. The crude product was purified by flash column chromatography on silica gel eluting with pentane:ethyl acetate (80:20, by volume) to provide the title compound (5.00 g) as a yellow oil.

후처리

  1. customat 0° C.
  2. customThe reaction mixture was quenched by the addition of water (100 ml)
  3. extractionthe aqueous phase was extracted with ether (2×50 ml)
  4. washThe combined organic phases were washed with water (30 ml) and brine (30 ml)
  5. dry with materialdried over magnesium sulphate
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customto leave a brown oil
  9. customThe crude product was purified by flash column chromatography on silica gel eluting with pentane:ethyl acetate (80:20, by volume)

출처 및 근거

ORD 기록
ord-51e2d01b55cc4feab979b99dc2235122
출처 데이터셋
uspto-grants-2006_09
특허 번호
US07109228B2

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