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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
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인쇄 미리보기

반응식

HRID 1282180 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

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

생성물 1

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

실험 절차

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.

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. additionWater was added to the residue
  3. extraction
the mixture was extracted with ethyl acetate
  • washThe extract was washed with brine
  • dry with materialdried over anhydrous sodium sulfate
  • customThe solvent was evaporated
  • 출처 및 근거

    ORD 기록
    ord-4645d9bdf4974fe59e40652d4b3a5c70
    출처 데이터셋
    uspto-grants-2002_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06455528B1

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