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Methyl iodide → 6-methoxy-1H-pyrrolo[2,3-b]pyridine

HRID 1515868
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HRID 1515868 반응식
[NH:1]1[C:5]2=[N:6][C:7]([OH:10])=[CH:8][CH:9]=[C:4]2[CH:3]=[CH:2]1.[C:11](=O)([O-])[O-].[K+].[K+].IC>CC(C)=O>[CH3:11][O:10][C:7]1[N:6]=[C:5]2[NH:1][CH:2]=[CH:3][C:4]2=[CH:9][CH:8]=1
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 178515692HCID 178515692, 화합물

생성물 1

HCID 116151916-methoxy-1H-pyrrolo[2,3-b]pyridine수율 30%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

A mixture of 1H-pyrrolo[2,3-b]pyridin-6-ol (1.52 g, 11.4 mmol) and potassium carbonate (7.86 g, 57 mmol) in acetone (100 mL) was stirred under nitrogen at room temperature for 1 h. Iodomethane (2.6 g, 18.2 mmol) was added and the resulting mixture stirred at 56° C. for 12 h. The mixture was filtered, and the filtrate was concentrated to half its volume, diluted with water, and extracted with dichloromethane. The combined organic layers were dried over anhydrous sodium sulfate and evaporated. The residue was purified by flash column chromatography (silica gel from QingDao, 200-300 mesh, 20% ethyl acetate/hexanes) to afford 6-methoxy-1H-pyrrolo[2,3-b]pyridine (0.5 g, 30%): LC/MS m/e calcd for C8H8N2O [M+H]+ 149.17, observed 149.1.

후처리

  1. stirringthe resulting mixture stirred at 56° C. for 12 h
  2. filtrationThe mixture was filtered
  3. concentrationthe filtrate was concentrated to half its volume
  4. additiondiluted with water
  5. extractionextracted with dichloromethane
  6. dry with materialThe combined organic layers were dried over anhydrous sodium sulfate
  7. customevaporated
  8. customThe residue was purified by flash column chromatography (silica gel from QingDao, 200-300 mesh, 20% ethyl acetate/hexanes)

출처 및 근거

ORD 기록
ord-2637bbeeb5e04698968ce4cd411c1d5e
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08222416B2

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