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1-Acetyl-4-(4,6-difluoropyrimidin-2-yl)piperazine → 1-Acetyl-4-(6-(dimethylamino)-4-fluoropyrimidin-2-yl)piperazine

HRID 1282180
ノート
印刷プレビュー

反応式

HRID 1282180 の反応式
[C:1]([N:4]1[CH2:9][CH2:8][N:7]([C:10]2[N:15]=[C:14](F)[CH:13]=[C:12]([F:17])[N:11]=2)[CH2:6][CH2:5]1)(=[O:3])[CH3:2].[CH3:18][NH:19][CH3:20].C(O)C>>[C:1]([N:4]1[CH2:5][CH2:6][N:7]([C:10]2[N:11]=[C:12]([F:17])[CH:13]=[C:14]([N:19]([CH3:20])[CH3:18])[N:15]=2)[CH2:8][CH2:9]1)(=[O:3])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 184230501-Acetyl-4-(4,6-difluoropyrimidin-2-yl)piperazineHCID 22184060Dimethylamine ethanol

生成物 1

HCID 184231721-Acetyl-4-(6-(dimethylamino)-4-fluoropyrimidin-2-yl)piperazine

実験手順

1-Acetyl-4-(4,6-difluoropyrimidin-2-yl)piperazine (1.9 g) was dissolved in 12% dimethylamine-ethanol solution (30 ml) and the mixture was stirred at room temperature for 1 hr. The reaction mixture was concentrated under reduced pressure. Water was added to the residue and the mixture was extracted with ethyl acetate. The extract was washed with brine and dried over anhydrous sodium sulfate. The solvent was evaporated to give the title compound (2.1 g) as a yellow solid.

後処理

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. additionWater was added to the residue
  3. extractionthe mixture was extracted with ethyl acetate
  • washThe extract was washed with brine
  • dry with materialdried over anhydrous sodium sulfate
  • customThe solvent was evaporated
  • 出典と根拠

    ORDレコード
    ord-4645d9bdf4974fe59e40652d4b3a5c70
    出典データセット
    uspto-grants-2002_09
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US06455528B1

    反応ノート

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