Hydrochloric Acid → 5-Bromo-2-methoxypyridin-3-amine

HRID 520605

反応式

HRID 520605 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([N+:10]([O-])=O)[C:5]([O:8][CH3:9])=[N:6][CH:7]=1.Cl>[Fe].O>[Br:1][C:2]1[CH:3]=[C:4]([NH2:10])[C:5]([O:8][CH3:9])=[N:6][CH:7]=1

参加物

5

反応条件

温度
22.5 °C

実験手順

Iron powder (1.17 kg) was added to a suspension of 5-bromo-2-(methyloxy)-3-nitropyridine (1.36 kg) in IMS (6.1 L), stirred under nitrogen at 20-25° C. Water (0.8 L) was then added and the mixture cooled to less than 10° C. Aqueous hydrochloric acid (0.8 L concentrated hydrochloric acid and 0.8 L water) was then added to the reaction mixture, maintaining the temperature below 10-15° C. The suspension was warmed to 20-25° C. and then stirred at this temperature for 23 hours. The suspension was filtered, the filter cake washed with IMS (2×2.7 L) and the combined filtrates concentrated under vacuum. Water (4.1 L) was added slowly to the concentrated solution and the resulting suspension was held at 20-25° C. for 1.75 hours. The resultant suspension was filtered, washed with water (2×6.8 L) and the solid dried under vacuum to give the title compound as an off-white solid (1.13 kg).

後処理

  1. temperaturethe mixture cooled to less than 10° C
  2. temperaturemaintaining the temperature below 10-15° C
  3. temperatureThe suspension was warmed to 20-25° C.
  4. stirringstirred at this temperature for 23 hours
  5. filtrationThe suspension was filtered
  6. washthe filter cake washed with IMS (2×2.7 L)
  7. concentrationthe combined filtrates concentrated under vacuum
  8. additionWater (4.1 L) was added slowly to the concentrated solution
  9. filtrationThe resultant suspension was filtered
  10. washwashed with water (2×6.8 L)
  11. customthe solid dried under vacuum

出典と根拠

ORDレコード
ord-3bd6b642172a45998b90e41cb3beb3a6
出典データセット
uspto-grants-2016_05
特許番号
US09326987B2

関連ノート

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