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Diethyl Sulfate → 1-Ethyl-1H-imidazo[4,5-b]pyridine

HRID 1926476
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HRID 1926476 반응식
[N:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[N:9][C:4]=2[NH:3][CH:2]=1.[H-].[Na+].[CH2:12](OS(OCC)(=O)=O)[CH3:13]>CN(C)C=O>[CH2:12]([N:1]1[C:5]2[C:4](=[N:9][CH:8]=[CH:7][CH:6]=2)[N:3]=[CH:2]1)[CH3:13]
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참가 물질

5

반응물 3

HCID 6163Diethyl SulfateHCID 24758Sodium hydrideHCID 178420746HCID 178420746, 화합물

생성물 1

HCID 217595471-Ethyl-1H-imidazo[4,5-b]pyridine수율 64.8%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a flask were added 0.5 g 4-azabenzimidazole and 10 ml N,N-dimethylformamide and the mixture was cooled to 10 C under nitrogen. 0.18 g Sodium hydride were added in portions and the reaction mixture was stirred for 20 minutes. 0.71 g Diethylsulfate were added and the mixture was allowed to warm to 22 C and was stirred for 16 hours. The mixture was quenched slowly with 30 ml 1M hydrochloric acid and the aqueous layer was washed with ethyl acetate. After basification with sodium hydroxide, the product was extracted twice with ethyl acetate and dried over sodium sulfate. Following filtration and solvent removal, the product was purified by silica gel chromatography using 5% methanol in ethyl acetate to 12% methanol in ethyl acetate. 0.4 g Of an oil was obtained.

후처리

  1. temperaturethe mixture was cooled to 10 C under nitrogen
  2. temperatureto warm to 22 C
  3. stirringwas stirred for 16 hours
  4. customThe mixture was quenched slowly with 30 ml 1M hydrochloric acid
  5. washthe aqueous layer was washed with ethyl acetate
  6. extractionAfter basification with sodium hydroxide, the product was extracted twice with ethyl acetate
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltration and solvent removal
  9. customthe product was purified by silica gel chromatography

출처 및 근거

ORD 기록
ord-8ea3ee8b0ff44335bcb7da25b59a2c55
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08182718B2

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