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Methyl acetoacetate → 6-Methyl-2-trifluoromethylpyrimidin-4-ol

HRID 1426359
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HRID 1426359 반응식
[F:1][C:2]([F:7])([F:6])[C:3](=[NH:5])[NH2:4].O=[C:9]([CH3:15])[CH2:10][C:11](OC)=[O:12].C[O-].[Na+]>CO>[CH3:15][C:9]1[N:4]=[C:3]([C:2]([F:7])([F:6])[F:1])[NH:5][C:11](=[O:12])[CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7757Methyl acetoacetateHCID 2776882TrifluoroacetamidineHCID 10942334Sodium Methoxide

생성물 1

HCID 1354086166-Methyl-2-trifluoromethylpyrimidin-4-ol

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 2,2,2-trifluoroethanimidamide (3.02 g, 22.9 mmol) and 3-oxobutanoic acid, methyl ester (2.60 mL, 24.0 mmol) in methanol (25 mL) was added 25 wt % sodium methoxide (10.5 mL, 45.8 mmol). The reaction solution was stirred at room temperature overnight. The solvent was removed in vacuo and diluted with ethyl acetate and 5M HCl. The aqueous layer was extracted with ethyl acetate once. The organic solutions were washed with brine, dried over sodium sulfate, filtered and concentrated. The residue was purified by flash chromatography on a silica gel column to give the desired product as white solid.

후처리

  1. customThe solvent was removed in vacuo
  2. additiondiluted with ethyl acetate and 5M HCl
  3. extractionThe aqueous layer was extracted with ethyl acetate once
  4. washThe organic solutions were washed with brine
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue was purified by flash chromatography on a silica gel column

출처 및 근거

ORD 기록
ord-9e17236e3edd4a4d8bda801d283cc8b7
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08933085B2

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