Potassium Iodide → Cgp 57698

HRID 1721170ノート

反応式

HRID 1721170 の反応式
[F:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][C:8]([CH2:12][O:13][C:14]3[CH:15]=[C:16]([CH:18]=[CH:19][CH:20]=3)[NH2:17])=[N:9]2)=[CH:4][CH:3]=1.[C:21](=[O:24])([O-])[O-:22].[Na+].[Na+].N[C:28]1C=[C:30]([OH:34])[CH:31]=[CH:32][CH:33]=1.Br[CH2:36][C:37]1C=CC2C(=CC(F)=CC=2)N=1.C(=O)([O-])[O-].[Cs+].[Cs+].[I-].[K+]>CC(C)=O>[F:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][C:8]([CH2:12][O:13][C:14]3[CH:15]=[C:16]([NH:17][C:30](=[O:34])[CH2:31][C:32]([CH2:33][CH3:28])([CH2:36][CH3:37])[C:21]([OH:22])=[O:24])[CH:18]=[CH:19][CH:20]=3)=[N:9]2)=[CH:4][CH:3]=1

参加物

8

実験手順

3-(7-fluoro-2-quinolinylmethoxy)aniline: 1.99 g of sodium carbonate are added to a solution of 1.36 g of 3-aminophenol in 150 ml of acetone and the batch is stirred for 15 min. at 20°. 3.0 g of 2-bromomethyl-7-fluoroquinoline, 4.07 g of caesium carbonate and 0.1 g of potassium iodide are added to the mixture which is boiled under reflux for 3 hours. The reaction mixture is filtered, the precipitate is washed with acetone and the filtrate is concentrated by evaporation. The residue is taken up in methylene chloride, washed with water, dried over sodium sulfate and concentrated by evaporation. The resulting orange oil is chromatographed on 200 g of silica gel using hexane/ethyl acetate 3:1. The title compound is obtained in the form of a yellow solid of m.p. 88°-89°.

後処理

  1. temperatureunder reflux for 3 hours
  2. filtrationThe reaction mixture is filtered
  3. washthe precipitate is washed with acetone
  4. concentrationthe filtrate is concentrated by evaporation
  5. washwashed with water
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated by evaporation
  8. customThe resulting orange oil is chromatographed on 200 g of silica gel

出典と根拠

ORDレコード
ord-1acb8656019445ec83dff57a6f7473bb
出典データセット
uspto-grants-1996_04
特許番号
US05508408

反応ノート

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