Ammonium Chloride → 5-Chloro-1-isopropyl-1H-pyrazol-4-amine

HRID 1487668ノート

反応式

HRID 1487668 の反応式
[Cl:1][C:2]1[N:6]([CH:7]([CH3:9])[CH3:8])[N:5]=[CH:4][C:3]=1[N+:10]([O-])=O.[Cl-].[NH4+]>CCO.[Fe]>[Cl:1][C:2]1[N:6]([CH:7]([CH3:9])[CH3:8])[N:5]=[CH:4][C:3]=1[NH2:10]

参加物

5

反応条件

温度
80 °C

実験手順

To a suspension of 5-chloro-1-isopropyl-4-nitro-1H-pyrazole (1 equiv) and iron dust (3 equiv) in EtOH (0.26 M) was added ammonium chloride (3 equiv). The mixture was heated to 80° C. for 20 h then cooled to room temperature. The reaction was quenched with solid sodium bicarbonate and treated with ethyl acetate (0.09 M) with continuous stirring. The mixture was filtered and the filter cake was rinsed with ethyl acetate. The combined filtrate was dried over sodium sulfate and concentrated under reduced pressure. The crude product was purified by silica gel chromatography (1.5% MeOH in DCM) to provide the desired product (76% yield) as a brown oil. MS (ESI) m/z 160.1 [M+H]+.

後処理

  1. temperaturethen cooled to room temperature
  2. customThe reaction was quenched with solid sodium bicarbonate
  3. additiontreated with ethyl acetate (0.09 M) with continuous stirring
  4. filtrationThe mixture was filtered
  5. washthe filter cake was rinsed with ethyl acetate
  6. dry with materialThe combined filtrate was dried over sodium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customThe crude product was purified by silica gel chromatography (1.5% MeOH in DCM)

出典と根拠

ORDレコード
ord-f8dece81f7534d85bec3b5fe082e7622
出典データセット
uspto-grants-2016_08
特許番号
US09428509B2

反応ノート

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