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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Bromine → 3-Bromo-2-ethyl-imidazo[1,2-a]pyridine

HRID 1357931
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반응식

HRID 1357931 반응식
[CH2:1]([C:3]1[N:4]=[C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][N:6]2[CH:11]=1)[CH3:2].[Br:12]Br>C(O)C.O>[Br:12][C:11]1[N:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]2=[N:4][C:3]=1[CH2:1][CH3:2]
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참가 물질

5

반응물 2

HCID 24408BromineHCID 218319912-Ethylimidazo[1,2-a]pyridine

생성물 1

HCID 219127413-Bromo-2-ethyl-imidazo[1,2-a]pyridine수율 66.8%

시약·촉매·용매 2

HCID 702Ethanol용매2회HCID 962Water용매

실험 절차

To a solution of 2-ethyl-imidazo[1,2-a]pyridine (2.17 g, 14.9 mmol) in ethanol (25 mL) was added bromine (2.0 g, 12.5 mmol) in water (5 mL) dropwise at rt. After stirring at rt for 4h, ethanol was evaporated under reduced pressure. The residue was basified with aqueous sodium bicarbonate and extracted with methylene chloride (3×). The organic phase was washed with brine and dried over anhydrous magnesium sulfate. Concentration followed by flash chromatography eluting with 20 % ethyl acetate in hexanes, followed by 50% ethyl acetate in hexanes afforded the title compound (1.88 g) as a viscous oil.

후처리

  1. customwas evaporated under reduced pressure
  2. extractionextracted with methylene chloride (3×)
  3. washThe organic phase was washed with brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationConcentration
  6. washeluting with 20 % ethyl acetate in hexanes

출처 및 근거

ORD 기록
ord-561312f5aed24479b2ebee4db8301ee2
출처 데이터셋
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06593346B2

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