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

HRID 1471223
ノート
印刷プレビュー

反応式

HRID 1471223 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6163Diethyl SulfateHCID 24758Sodium hydrideHCID 178420746HCID 178420746、化合物

生成物 1

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

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-2790bfc8b6e34c5fa15b52b1d2df4828
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09011734B2

反応ノート

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