Hydrochloric Acid → 2-Chloro-4-methoxypyridin-3-amine

HRID 550834

反応式

HRID 550834 の反応式
[NH2:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[O:8][CH3:9].OO.C(OCC)(=O)C.CCCCCC.[ClH:24]>>[NH2:1][C:2]1[C:3]([Cl:24])=[N:4][CH:5]=[CH:6][C:7]=1[O:8][CH3:9]

参加物

5

実験手順

To a magnetically stirred mixture of 3-Amino-4-methoxypyridine (4.45 g, 35.89 mmole) in 12N HCl (25 mL) cooled in an ice bath was added hydrogen peroxide (5.3 g, 46.65 mmol, 30% solution). The reaction was allowed to slowly warm to room temperature and stirred for 1 h. TLC (50% ethyl acetate/hexane) indicated complete consumption of starting material. The reaction mixture was slowly poured into saturated sodium bicarbonate solution (400 mL) to neutralize the reaction and extracted with ethyl acetate. The resulting organic layers were washed with saturated sodium chloride solution and dried over magnesium sulfate. Filtration and concentration gave 3-Amino-2-chloro-4 methoxypyridine (4.56 g, 28.77 mmol, 80% yield) as an orange solid.

後処理

  1. temperaturecooled in an ice bath
  2. customconsumption of starting material
  3. additionThe reaction mixture was slowly poured into saturated sodium bicarbonate solution (400 mL)
  4. customthe reaction
  5. extractionextracted with ethyl acetate
  6. washThe resulting organic layers were washed with saturated sodium chloride solution
  7. dry with materialdried over magnesium sulfate
  8. filtrationFiltration and concentration

出典と根拠

ORDレコード
ord-2548548e228445b1832b59a62bec1785
出典データセット
uspto-grants-2011_05
特許番号
US07947692B2

関連ノート

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