Iodine chloride → 4-Bromo-5-chloro-3-iodopyridin-2-amine

HRID 1521950ノート

反応式

HRID 1521950 の反応式
[Br:1][C:2]1[C:7]([Cl:8])=[CH:6][N:5]=[C:4]([NH2:9])[CH:3]=1.[I:10]Cl>CN(C)C=O>[Br:1][C:2]1[C:7]([Cl:8])=[CH:6][N:5]=[C:4]([NH2:9])[C:3]=1[I:10]

参加物

4

反応条件

温度
40 °C

実験手順

A solution of Example 52A (3 g, 14.46 mmol) in N,N-dimethylformamide (60 mL) was heated to 40° C. and iodine chloride (2.82 g, 17.35 mmol) was added. After stirring at 40° C. for 3 hours, a second lot of iodine chloride (2.82 g, 17.35 mmol) was added and the mixture was stirred overnight at 40° C. The mixture was cooled to room temperature and quenched with ice cold water. The mixture was extracted with ethyl acetate (100 mL×2) and the organic layer was washed with water and brine, dried over sodium sulfate, filtered, and concentrated. Purification by column chromatography (silica gel, 20% ethyl acetate in hexane) afforded the title compound. LCMS: 334.6 (M+H)+.

後処理

  1. stirringthe mixture was stirred overnight at 40° C
  2. temperatureThe mixture was cooled to room temperature
  3. customquenched with ice cold water
  4. extractionThe mixture was extracted with ethyl acetate (100 mL×2)
  5. washthe organic layer was washed with water and brine
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customPurification by column chromatography (silica gel, 20% ethyl acetate in hexane)

出典と根拠

ORDレコード
ord-18667432085846408bc3ff2246f46f8a
出典データセット
uspto-grants-2015_07
特許番号
US09073922B2

反応ノート

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