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3,5-Dimethylpyrazole → HCID 12926677、化合物

HRID 1916049
ノート
印刷プレビュー

反応式

HRID 1916049 の反応式
[CH3:1][C:2]1[CH:6]=[C:5]([CH3:7])[NH:4][N:3]=1.[H-].[Na+].[Cl:10][C:11]1[CH:16]=[C:15]([Cl:17])[N:14]=[C:13](S(C)(=O)=O)[N:12]=1>ClCCl>[Cl:10][C:11]1[CH:16]=[C:15]([Cl:17])[N:14]=[C:13]([N:3]2[C:2]([CH3:1])=[CH:6][C:5]([CH3:7])=[N:4]2)[N:12]=1
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

5

反応物 3

HCID 62103,5-DimethylpyrazoleHCID 24758Sodium hydrideHCID 2396854,6-Dichloro-2-(methylsulfonyl)pyrimidine

生成物 1

HCID 12926677HCID 12926677、化合物収率 59%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

反応条件

温度
-78 °C

実験手順

A suspension of 3,5-dimethylpyrazole (3.9 g, 40.7 mmol) and sodium hydride (60% in mineral oil, 1.7 g) in dichloromethane (50 mL) was added dropwise to a cooled (−78° C.) solution of 4,6-dichloro-2-methanesulfonyl-pyrimidine (10 g, 38.7 mmol) in dichloromethane (200 mL). The mixture was stirred at −78° C. for one hour. The reaction was carefully quenched at the same temperature by addition of water (150 mL). The mixture was allowed to warm to room-temperature. Brine (150 mL) was added and the phases were separated. The aqueous phase was extracted with dichloromethane (4×200 mL). The combined organic layers were washed with brine, dried over sodium sulphate, filtrated and concentrated in vacuo. The crude product was purified by flash chromatography (ethyl acetate/heptane as eluent) to give 4,6-dichloro-2-(3,5-dimethyl-pyrazol-1-yl)-pyrimidine (5.5 g, 59%) as a white crystalline compound.

後処理

  1. additionwas added dropwise to
  2. customThe reaction was carefully quenched at the same temperature by addition of water (150 mL)
  3. temperatureto warm to room-temperature
  4. additionBrine (150 mL) was added
  5. customthe phases were separated
  6. extractionThe aqueous phase was extracted with dichloromethane (4×200 mL)
  7. washThe combined organic layers were washed with brine
  8. dry with materialdried over sodium sulphate
  9. filtrationfiltrated
  10. concentrationconcentrated in vacuo
  11. customThe crude product was purified by flash chromatography (ethyl acetate/heptane as eluent)

出典と根拠

ORDレコード
ord-2bd0d8372f0842048a4f17ac515aaa83
出典データセット
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08618099B2

反応ノート

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