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Uracil → HCID 86723841、化合物

HRID 576742
ノート
印刷プレビュー

反応式

HRID 576742 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

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

生成物 1

HCID 86723841HCID 86723841、化合物収率 4.8%

試薬・触媒・溶媒 2

HCID 8895Cupric acetate触媒HCID 86634112HCID 86634112、化合物
溶媒

実験手順

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).

後処理

  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)

出典と根拠

ORDレコード
ord-004422eaae934a5581d4b278f35941d4
出典データセット
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09040516B2

反応ノート

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