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

HRID 1091350
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HRID 1091350 반응식
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
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참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 178481675HCID 178481675, 화합물

생성물 1

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

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 (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.

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-b172098ee8a347979fe670c8cf9740ec
출처 데이터셋
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08129377B2

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