Allyl bromide → HCID 9967065、化合物

HRID 2215312ノート

反応式

HRID 2215312 の反応式
[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]

参加物

5

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-51e2d01b55cc4feab979b99dc2235122
出典データセット
uspto-grants-2006_09
特許番号
US07109228B2

反応ノート

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