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Dimethylformamide → Methyl 3-(4-fluorophenethyl)-6-hydroxypyridin-2-carboxylate

HRID 1251921
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HRID 1251921 반응식
[F:1][C:2]1[CH:20]=[CH:19][C:5]([CH2:6][CH2:7][C:8]2[C:9]([C:15]([O:17][CH3:18])=[O:16])=[N+:10]([O-])[CH:11]=[CH:12][CH:13]=2)=[CH:4][CH:3]=1.CN(C=[O:25])C>FC(F)(F)C(OC(=O)C(F)(F)F)=O>[F:1][C:2]1[CH:20]=[CH:19][C:5]([CH2:6][CH2:7][C:8]2[C:9]([C:15]([O:17][CH3:18])=[O:16])=[N:10][C:11]([OH:25])=[CH:12][CH:13]=2)=[CH:4][CH:3]=1
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참가 물질

4

반응물 2

HCID 6228DimethylformamideHCID 183244604-Fluorophenethyl-2-(methoxycarbonyl)pyridine-1-oxide

생성물 1

HCID 178499128Methyl 3-(4-fluorophenethyl)-6-hydroxypyridin-2-carboxylate

시약·촉매·용매 1

HCID 9845Trifluoroacetic anhydride용매

실험 절차

A solution of 3-(4-fluorophenethyl)-2-(methoxycarbonyl)pyridine-1-oxide (7.96 g) in DMF (100 ml) and trifluoroacetic anhydride (40.9 ml) was stirred under an inert atmosphere at ambient temperature for 24 hours. The reaction mixture was concentrated under reduced pressure, diluted with saturated aqueous sodium bicarbonate (150 ml) and extracted with dichloromethane (3×100 ml). The combined organic extracts were dried and concentrated under reduced pressure and the residue purified on a silica flash column eluting with methanol/dichloromethane (1:9) to give methyl 3-(4-fluorophenethyl)-6-hydroxypyridin-2-carboxylate as a cream solid (7.7 g).

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. additiondiluted with saturated aqueous sodium bicarbonate (150 ml)
  3. extractionextracted with dichloromethane (3×100 ml)
  4. customThe combined organic extracts were dried
  5. concentrationconcentrated under reduced pressure
  6. customthe residue purified on a silica flash column
  7. washeluting with methanol/dichloromethane (1:9)

출처 및 근거

ORD 기록
ord-cffeb43acb2444b8b09cebe752006caa
출처 데이터셋
uspto-grants-2002_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06342765B1

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