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5-Chloro-2-(2-fluoro-6-methoxy-phenoxy)-3-nitro-pyridine → 5-Chloro-2-(2-fluoro-6-methoxy-phenoxy)-pyridin-3-ylamine

HRID 419045
ノート
印刷プレビュー

反応式

HRID 419045 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([N+:18]([O-])=O)[C:5]([O:8][C:9]2[C:14]([O:15][CH3:16])=[CH:13][CH:12]=[CH:11][C:10]=2[F:17])=[N:6][CH:7]=1>CC(O)=O.CCOC(C)=O.[Fe]>[Cl:1][C:2]1[CH:3]=[C:4]([NH2:18])[C:5]([O:8][C:9]2[C:14]([O:15][CH3:16])=[CH:13][CH:12]=[CH:11][C:10]=2[F:17])=[N:6][CH:7]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 1

HCID 666488545-Chloro-2-(2-fluoro-6-methoxy-phenoxy)-3-nitro-pyridine

生成物 1

HCID 579422525-Chloro-2-(2-fluoro-6-methoxy-phenoxy)-pyridin-3-ylamine

試薬・触媒・溶媒 3

HCID 23925Iron触媒HCID 176Acetic Acid溶媒2 回HCID 8857Ethyl Acetate溶媒

反応条件

温度
80 °C

実験手順

AcOH (30 mL) and iron powder (5 g) were charged into a round bottom flask equipped with a magnetic stirring bar and warmed to 80° C. A solution of crude 5-chloro-2-(2-fluoro-6-methoxy-phenoxy)-3-nitro-pyridine in AcOH was added slowly into the mixture, keeping the temperature under 85° C. The reaction mixture was then cooled to room temperature, diluted with EtOAc, and filtered through a pad of Celite. The filtrate was concentrated under reduced pressure and the residue was partitioned between NaHCO3 and EtOAc. The organic portion was separated and the aqueous portion was extracted with EtOAc. The combined extracts were dried (Na2SO4), filtered, and concentrated under reduced pressure. The residue was purified by flash column chromatography on silica gel to provide 5-chloro-2-(2-fluoro-6-methoxy-phenoxy)-pyridin-3-ylamine (3.56 g) as a colorless powder.

後処理

  1. customequipped with a magnetic stirring bar
  2. customunder 85° C
  3. temperatureThe reaction mixture was then cooled to room temperature
  4. filtrationfiltered through a pad of Celite
  5. concentrationThe filtrate was concentrated under reduced pressure
  6. customthe residue was partitioned between NaHCO3 and EtOAc
  7. customThe organic portion was separated
  8. extractionthe aqueous portion was extracted with EtOAc
  9. dry with materialThe combined extracts were dried (Na2SO4)
  10. filtrationfiltered
  11. concentrationconcentrated under reduced pressure
  12. customThe residue was purified by flash column chromatography on silica gel

出典と根拠

ORDレコード
ord-95a34d98c24744afba09b1ad0c63943c
出典データセット
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08093247B2

反応ノート

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