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Methyl iodide → 3-Bromo-5-chloro-1-methylpyridin-2(1H)-one

HRID 1936448
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HRID 1936448 반응식
[Br:1][C:2]1[C:3](=[O:9])[NH:4][CH:5]=[C:6]([Cl:8])[CH:7]=1.[C:10](=O)([O-])[O-].[K+].[K+].IC>COCCOC>[Br:1][C:2]1[C:3](=[O:9])[N:4]([CH3:10])[CH:5]=[C:6]([Cl:8])[CH:7]=1
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 27267913-Bromo-5-chloropyridin-2-ol

생성물 1

HCID 223820353-Bromo-5-chloro-1-methylpyridin-2(1H)-one수율 74.6%

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

실험 절차

A mixture of 3-bromo-5-chloro-1H-2-pyridone (930 mg, 4.46 mmol), potassium carbonate (1.25 g, 9.1 mmol) and iodomethane (2.8 mL, 45 mmol) in 10 mL of DME was heated to reflux for 18 hr. The mixture was filtered hot and concentrated. The residue was recrystallized from ethyl acetate to give 3-bromo-5-chloro-1-methyl-2-pyridone (740 mg, 74%), mp 162-163° C. HRMS (C6H5BrClNO): Obs. Mass 220.9249. Calcd. Mass 220.9243 (M+H).

후처리

  1. temperaturewas heated
  2. temperatureto reflux for 18 hr
  3. filtrationThe mixture was filtered hot
  4. concentrationconcentrated
  5. customThe residue was recrystallized from ethyl acetate

출처 및 근거

ORD 기록
ord-fafc29b3859d46bd939a1a61e51f9b4a
출처 데이터셋
uspto-grants-2002_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06388084B1

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