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Hydrazine hydrate (1:1) → 5-Bromo-6-fluoro-3-methyl-1H-indazole

HRID 1497391
ノート
印刷プレビュー

反応式

HRID 1497391 の反応式
[Br:1][C:2]1[C:3]([F:12])=[CH:4][C:5](F)=[C:6]([C:8](=O)[CH3:9])[CH:7]=1.O.[NH2:14][NH2:15]>C(O)CO>[Br:1][C:2]1[CH:7]=[C:6]2[C:5](=[CH:4][C:3]=1[F:12])[NH:15][N:14]=[C:8]2[CH3:9]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24654Hydrazine hydrate (1:1)HCID 207853591-(5-Bromo-2,4-difluorophenyl)ethan-1-one

生成物 1

HCID 1784343175-Bromo-6-fluoro-3-methyl-1H-indazole収率 67%

試薬・触媒・溶媒 1

HCID 174Ethylene Glycol溶媒

反応条件

温度
160 °C

実験手順

To a solution of 1-(5-bromo-2,4-difluorophenyl)ethanone (4.9 g) in ethylene glycol (15 ml) was added hydrazine monohydrate (1.2 g) at room temperature, and the mixture was stirred at 160° C. for 26 hr. The reaction mixture was cooled to room temperature, and the insoluble material was removed. The filtrate was added to water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous ammonium chloride solution, saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (3.2 g).

後処理

  1. temperatureThe reaction mixture was cooled to room temperature
  2. customthe insoluble material was removed
  3. additionThe filtrate was added to water
  4. extractionthe mixture was extracted with ethyl acetate
  5. washThe organic layer was washed with saturated aqueous ammonium chloride solution, saturated aqueous sodium hydrogen carbonate solution and saturated brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customThe residue was purified by silica gel column chromatography (hexane/ethyl acetate)

出典と根拠

ORDレコード
ord-89e54050dfe84339a4669b430a964202
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09199963B2

反応ノート

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