Methyl iodide → 5-(2-Fluoropyridin-3-yl)-1-methylazepan-2-one

HRID 1880119노트

반응식

HRID 1880119 반응식
[F:1][C:2]1[C:7]([CH:8]2[CH2:14][CH2:13][NH:12][C:11](=[O:15])[CH2:10][CH2:9]2)=[CH:6][CH:5]=[CH:4][N:3]=1.[H-].[Na+].I[CH3:19].[Cl-].[NH4+]>CN(C=O)C>[F:1][C:2]1[C:7]([CH:8]2[CH2:14][CH2:13][N:12]([CH3:19])[C:11](=[O:15])[CH2:10][CH2:9]2)=[CH:6][CH:5]=[CH:4][N:3]=1

참가 물질

6

반응물 4

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 593268345-(2-Fluoropyridin-3-yl)azepan-2-one

생성물 1

HCID 593270605-(2-Fluoropyridin-3-yl)-1-methylazepan-2-one

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of 5-(2-fluoropyridin-3-yl)azepan-2-one (0.15 g, 0.72 mmol) in DMF (2.5 mL) under argon was added sodium hydride (0.021 g, 0.86 mmol). The mixture was stirred at room temperature for 15 min before iodomethane (0.054 mL, 0.86 mmol) was added via syringe. This mixture was stirred for 4 h at room temperature before saturated aqueous ammonium chloride was added. The mixture was extracted with ethyl acetate (2×) and the combined extracts were washed with water (3×), saturated aqueous sodium chloride (1×), dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to give 5-(2-fluoropyridin-3-yl)-1-methylazepan-2-one. [M+1]=223.1.

후처리

  1. additionwas added via syringe
  2. additionwas added
  3. extractionThe mixture was extracted with ethyl acetate (2×)
  4. washthe combined extracts were washed with water (3×), saturated aqueous sodium chloride (1×)
  5. dry with materialdried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-0f6cd8449a6d43e68a96c52e12f2ca43
출처 데이터셋
uspto-grants-2012_11
특허 번호
US08318718B2

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