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Uracil → HCID 86723841, 화합물

HRID 576742
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HRID 576742 반응식
[NH:1]1[CH:8]=[CH:7][C:5](=[O:6])[NH:4][C:2]1=[O:3].CN(CCN(C)C)C.[F:17][C:18]([F:29])([F:28])[C:19]1[CH:20]=[C:21](B(O)O)[CH:22]=[CH:23][CH:24]=1>CO.CN(C)C=O.O.C([O-])(=O)C.[Cu+2].C([O-])(=O)C>[F:17][C:18]([F:29])([F:28])[C:19]1[CH:24]=[C:23]([N:1]2[CH:8]=[CH:7][C:5](=[O:6])[NH:4][C:2]2=[O:3])[CH:22]=[CH:21][CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 1174UracilHCID 8037N,N,N',N'-TetramethylethylenediamineHCID 27343883-(Trifluoromethyl)phenylboronic acid

생성물 1

HCID 86723841HCID 86723841, 화합물수율 4.8%

시약·촉매·용매 2

HCID 8895Cupric acetate촉매HCID 86634112HCID 86634112, 화합물
용매

실험 절차

To a solution of uracil (8.9 g), copper(II) acetate (9.6 g), N,N,N,N-tetramethylethylenediamine (10.2 ml) in methanol/dimethy formamide/water (500/100/100 ml) was added 3-trifluoromethylphenyl boronic acid (10.0 g) and the resulting mixture was stirred at room temperature for twelve hours. The reaction mixture was concentrated under reduced pressure so as to remove methanol and thereto was added water (100 ml). The resulting mixture was extracted with ethyl acetate (100 ml×3) and the organic layer was washed with water (100 ml×2) and saturated saline (50 ml), dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate) to afford 1-(3-trifluoromethylphenyl)pyrimidin-2,4(1H,3H)-dione (650.0 mg).

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure so as
  2. customto remove methanol
  3. additionwas added water (100 ml)
  4. extractionThe resulting mixture was extracted with ethyl acetate (100 ml×3)
  5. washthe organic layer was washed with water (100 ml×2) and saturated saline (50 ml)
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customThe residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate)

출처 및 근거

ORD 기록
ord-004422eaae934a5581d4b278f35941d4
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09040516B2

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