Stannous Chloride → 2-Bromo-5-fluoropyridin-3-amine

HRID 2409035

反応式

HRID 2409035 の反応式
[Br:1][C:2]1[C:7]([N+:8]([O-])=O)=[CH:6][C:5]([F:11])=[CH:4][N:3]=1.Cl[Sn]Cl>CCO.Cl>[Br:1][C:2]1[C:7]([NH2:8])=[CH:6][C:5]([F:11])=[CH:4][N:3]=1

参加物

5

反応条件

温度
60 °C

実験手順

A suspension of 2-bromo-5-fluoro-3-nitropyridine (4.42 g, 20 mmol) and SnCl2 (22.56 g, 100 mmol) in EtOH (40 mL) and concentrated HCl (40 mL) was heated at 60° C. for 1 h. The reaction mixture was concentrated under reduced pressure. To the residue was added EtOAc (100 mL) and sat'd aq. NaHCO3 solution (200 mL), and the mixture was filtered with Celite® and extracted with EtOAc (100 mL×3). The organic layer was washed with saturated NaHCO3, water and brine, dried (MgSO4), filtered, and concentrated under reduced pressure to afford 3.1 g (80%) of 2-bromo-5-fluoropyridin-3-amine as a brown solid. MS (ESI): m/z=191.1 [M+1]+.

後処理

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. additionTo the residue was added EtOAc (100 mL)
  3. filtrationthe mixture was filtered with Celite®
  4. extractionextracted with EtOAc (100 mL×3)
  5. washThe organic layer was washed with saturated NaHCO3, water and brine
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-f9fefd6e1f4e4c79b7cca736daa2e513
出典データセット
uspto-grants-2014_08
特許番号
US08815877B2

関連ノート

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