Chloroform → HCID 86708205、化合物

HRID 533610

反応式

HRID 533610 の反応式
[Br:1][C:2]1[CH:3]=[C:4]2[N:10]=[C:9]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3SCC)[N:8]([CH3:20])[C:5]2=[N:6][CH:7]=1.C(Cl)(Cl)Cl.Cl[C:26]1C=CC=C(C(OO)=O)[CH:27]=1.[S:36]([O-:40])([O-])(=[O:38])=S.[Na+].[Na+]>O>[Br:1][C:2]1[CH:3]=[C:4]2[N:10]=[C:9]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[S:36]([CH2:26][CH3:27])(=[O:40])=[O:38])[N:8]([CH3:20])[C:5]2=[N:6][CH:7]=1

参加物

6

実験手順

To a mixture of 6-bromo-2-(2-ethylsulfanylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridine (0.20 g) and chloroform (3 ml), 3-chloroperbenzoic acid (purity: not less than 65%) (0.34 g) was added under ice-cooling, and then heated to room temperature, and stirred for 3.5 hours. Chloroform and saturated aqueous sodium thiosulfate solution were poured thereinto under ice-cooling, and stirred, and then, water was poured, and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The resulting solid was washed with hexane, and dried to give 0.20 g of 6-bromo-2-(2-ethylsulfonylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridine (hereinafter referred to as Present Compound 44).

後処理

  1. additionwas added under ice-
  2. temperaturecooling
  3. temperatureunder ice-cooling
  4. stirringstirred
  5. extractionextracted with ethyl acetate
  6. washThe organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine
  7. dry with materialdried over sodium sulfate
  8. concentrationconcentrated under reduced pressure
  9. washThe resulting solid was washed with hexane
  10. customdried

出典と根拠

ORDレコード
ord-ddba5269e00c4fa9a96e7cb3ef2aa64b
出典データセット
uspto-grants-2014_10
特許番号
US08853238B2

関連ノート

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