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Phosphorus oxychloride → 2-Chloro-3-methyl-6-(3-fluoropyridin-4-yl)-3H-pyrimidin-4-one

HRID 1091350
ノート
印刷プレビュー

反応式

HRID 1091350 の反応式
P(Cl)(Cl)([Cl:3])=O.[F:6][C:7]1[CH:8]=[N:9][CH:10]=[CH:11][C:12]=1[C:13]1[N:18]=[C:17](S)[N:16]([CH3:20])[C:15](=[O:21])[CH:14]=1>CN(C)C=O>[Cl:3][C:17]1[N:16]([CH3:20])[C:15](=[O:21])[CH:14]=[C:13]([C:12]2[CH:11]=[CH:10][N:9]=[CH:8][C:7]=2[F:6])[N: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

4

反応物 2

HCID 24813Phosphorus oxychlorideHCID 178481675HCID 178481675、化合物

生成物 1

HCID 595768122-Chloro-3-methyl-6-(3-fluoropyridin-4-yl)-3H-pyrimidin-4-one収率 73.3%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
60 °C

実験手順

After one hour stirring of a solution of phosphorus oxychloride (45 g, 293 mmol) in dimethylformamide (450 ml) at room temperature, 6-(3-fluoropyridin-4-yl)-2-mercapto-3-methyl-3H-pyrimidin-4-one (46.3 g, 195 mmol) was added and heated at 60° C. for 2 hours. The resulting suspension was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate. The aqueous layer was extracted with ethyl acetate and the combined organic layer was washed with brine, dried over magnesium sulfate, and concentrated in vacuo. The residue was washed by hexane to furnish 2-chloro-6-(3-fluoropyridin-4-yl)-3-methyl-3H-pyrimidin-4-one (34.2 g, 143 mmol, 73%) as white crystals.

後処理

  1. customThe resulting suspension was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate
  2. extractionThe aqueous layer was extracted with ethyl acetate
  3. washthe combined organic layer was washed with brine
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated in vacuo
  6. washThe residue was washed by hexane

出典と根拠

ORDレコード
ord-b172098ee8a347979fe670c8cf9740ec
出典データセット
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08129377B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート