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Phosphorus oxychloride → HCID 86233545, 화합물

HRID 1091351
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HRID 1091351 반응식
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
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참가 물질

4

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HCID 24813Phosphorus oxychlorideHCID 1784816776-(2,3-dichloropyridin-4-yl)-2-mercapto-3-methyl-3H-pyrimidin-4-one

생성물 1

HCID 86233545HCID 86233545, 화합물수율 72.2%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
60 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-f56536f0af64418e9c225498fbd32d2f
출처 데이터셋
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08129377B2

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