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Trimethylsilyl iodide → 3-(Difluoromethyl)-1-(5-fluoropyrimidin-2-yl)-1H-pyrazole-4-carboxylic acid

HRID 2279613
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인쇄 미리보기

반응식

HRID 2279613 반응식
[F:1][CH:2]([F:20])[C:3]1[C:7]([C:8]([O:10]CC)=[O:9])=[CH:6][N:5]([C:13]2[N:18]=[CH:17][C:16]([F:19])=[CH:15][N:14]=2)[N:4]=1.I[Si](C)(C)C>>[F:20][CH:2]([F:1])[C:3]1[C:7]([C:8]([OH:10])=[O:9])=[CH:6][N:5]([C:13]2[N:18]=[CH:17][C:16]([F:19])=[CH:15][N:14]=2)[N:4]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 85247Trimethylsilyl iodideHCID 59579960Ethyl 3-(difluoromethyl)-1-(5-fluoropyrimidin-2-yl)-1H-pyrazole-4-carboxylate

생성물 1

HCID 595798213-(Difluoromethyl)-1-(5-fluoropyrimidin-2-yl)-1H-pyrazole-4-carboxylic acid

반응 조건

온도
90 °C

실험 절차

A mixture of ethyl 3-(difluoromethyl)-1-(5-fluoropyrimidin-2-yl)-1H-pyrazole-4-carboxylate (50 mg) and iodotrimethylsilane (1.0 mL) is heated at 90° C. for 4 h. The mixture is concentrated under vacuum, quenched with ice, and sodium metabisulfite is added until the aqueous solution becomes colorless. The mixture is then extracted with EtOAc (3×10 mL) and dried over anhydrous MgSO4. The dried extract is filtered and concentrated under vacuum to afford the title compound as white solid.

후처리

  1. concentrationThe mixture is concentrated under vacuum
  2. customquenched with ice, and sodium metabisulfite
  3. additionis added until the aqueous solution
  4. extractionThe mixture is then extracted with EtOAc (3×10 mL)
  5. dry with materialdried over anhydrous MgSO4
  6. extractionThe dried extract
  7. filtrationis filtered
  8. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-da5d7568124242c7b478ac0bf384417a
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09133204B2

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