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Phosphorus oxychloride → HCID 86233545、化合物

HRID 1091351
ノート
印刷プレビュー

反応式

HRID 1091351 の反応式
P(Cl)(Cl)([Cl:3])=O.[Cl:6][C:7]1[C:12]([Cl:13])=[C:11]([C:14]2[N:19]=[C:18](S)[N:17]([CH3:21])[C:16](=[O:22])[CH:15]=2)[CH:10]=[CH:9][N:8]=1>CN(C)C=O>[Cl:3][C:18]1[N:17]([CH3:21])[C:16](=[O:22])[CH:15]=[C:14]([C:11]2[CH:10]=[CH:9][N:8]=[C:7]([Cl:6])[C:12]=2[Cl:13])[N:19]=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 1784816776-(2,3-dichloropyridin-4-yl)-2-mercapto-3-methyl-3H-pyrimidin-4-one

生成物 1

HCID 86233545HCID 86233545、化合物収率 72.2%

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 (2.9 g, 18.9 mmol) in dimethylformamide (30 ml) at room temperature, 6-(2,3-dichloropyridin-4-yl)-2-mercapto-3-methyl-3H-pyrimidin-4-one (3.58 g, 12.4 mmol) was added and heated at 60° C. for 2 hours. The resulting suspension was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate and the aqueous layer was extracted with ethyl acetate. 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-(2,3-dichloropyridin-4-yl)-3-methyl-3H-pyrimidin-4-one (2.6 g, 8.95 mmol, 72%) 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-f56536f0af64418e9c225498fbd32d2f
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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