Dimethyl Sulfate → 3-(4-Choro-2-nitrophenyl)-1-methyl-6-trifluoromethyl-2,4(1h, 3h)-pyrimidinedione

HRID 1271762ノート

反応式

HRID 1271762 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:13](=[O:14])[CH:12]=[C:11]([C:15]([F:18])([F:17])[F:16])[NH:10][C:9]2=[O:19])=[C:4]([N+:20]([O-:22])=[O:21])[CH:3]=1.S(OC)(O[CH3:27])(=O)=O.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:13](=[O:14])[CH:12]=[C:11]([C:15]([F:17])([F:18])[F:16])[N:10]([CH3:27])[C:9]2=[O:19])=[C:4]([N+:20]([O-:22])=[O:21])[CH:3]=1

参加物

5

反応条件

温度
55 °C

実験手順

A mixture of 3-(4-chloro-2-nitrophenyl)-6-trifluoromethyl-2,4(1H, 3H)-pyrimidinedione (3 g), dimethyl sulfate (1.7 g) and potassium carbonate (1.85 g) in N,N-dimethylformamide (100 ml) was stirred at 55° C. overnight. The resulting mixture was allowed to cool to ambient temperature and filtered through Celite to remove unsoluble precipitate. The filtrate was diluted with a mixed solvent of ethyl acetate and hexane (1:1, 200 ml), washed with brine (×2) and dried over anhydrous sodium sulfate. After removal of the solvent, the residue was solidified. The yellow solid was recrystallized from ethyl acetate and hexane to give desired compound (2.3 g).

後処理

  1. temperatureto cool to ambient temperature
  2. filtrationfiltered through Celite
  3. customto remove unsoluble precipitate
  4. additionThe filtrate was diluted with a mixed solvent of ethyl acetate and hexane (1:1, 200 ml)
  5. washwashed with brine (×2)
  6. dry with materialdried over anhydrous sodium sulfate
  7. customAfter removal of the solvent
  8. customThe yellow solid was recrystallized from ethyl acetate and hexane

出典と根拠

ORDレコード
ord-f8d595737c0643eba9602612ca8aadca
出典データセット
uspto-grants-2007_04
特許番号
USRE039590E1

反応ノート

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