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Dimethylformamide → 1-(3-Chloro-2-pyridyl)-3-methyl-pyrazole-4-carbaldehyde

HRID 1517597
ノート
印刷プレビュー

反応式

HRID 1517597 の反応式
[CH3:1][C:2]1[C:6]([CH:7]=[O:8])=[CH:5][NH:4][N:3]=1.C(=O)([O-])[O-].[K+].[K+].FN1C=C[CH:19]=[CH:18][CH:17]1[Cl:22].[CH3:23][N:24]([CH3:27])C=O>O>[Cl:22][C:17]1[C:23]([N:4]2[CH:5]=[C:6]([CH:7]=[O:8])[C:2]([CH3:1])=[N:3]2)=[N:24][CH:27]=[CH:19][CH:18]=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

6

反応物 4

HCID 6228DimethylformamideHCID 11430Potassium CarbonateHCID 866535441-Fluoro-2-chloropyridineHCID 1784345503-methyl-1H-pyrazole-4-carbaldehyde

生成物 1

HCID 582685431-(3-Chloro-2-pyridyl)-3-methyl-pyrazole-4-carbaldehyde収率 52%

試薬・触媒・溶媒 1

HCID 962
Water
溶媒

反応条件

温度
40 °C

実験手順

To a solution of 3-methyl-pyrazole-4-carbaldehyde (0.5 g, 4.5 mmol) in dry dimethylformamide (15 mL) is added potassium carbonate (2.5 g, 18 mmol,) at room temperature. The reaction mixture is stirred at 40° C. for 30 min and then 1-fluoro-2-chloropyridine (0.77 g, 6 mmol,) is added. The reaction mixture is heated at 70° C. for 16 h. After completion, the reaction mixture is cooled to room temperature, diluted with water and then extracted with ethyl acetate. The organic layer is dried over sodium sulfate, filtered and concentrated under reduce pressure. The crude mixture is purified by chromatography on silica gel eluting with hexane/ethyl acetate (75:25, 65:35) to yield 0.525 g (52%) of the title compound. MS (m/z): 222 (M+1).

後処理

  1. temperatureThe reaction mixture is heated at 70° C. for 16 h
  2. temperatureAfter completion, the reaction mixture is cooled to room temperature
  3. extractionextracted with ethyl acetate
  4. dry with materialThe organic layer is dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude mixture is purified by chromatography on silica gel eluting with hexane/ethyl acetate (75:25, 65:35)

出典と根拠

ORDレコード
ord-b20cf038e506491fad97d4ca41cc6b6b
出典データセット
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08232289B2

反応ノート

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