m-Chloroperbenzoic acid → HCID 86644470、化合物

HRID 2404539ノート

反応式

HRID 2404539 の反応式
[Cl:1][C:2]1[C:3]([O:23][C:24]([F:32])([F:31])[CH:25]([F:30])[C:26]([F:29])([F:28])[F:27])=[N:4][N:5]([C:9]2[CH:14]=[C:13]([S:15][CH2:16][C:17]([F:20])([F:19])[F:18])[C:12]([CH3:21])=[CH:11][C:10]=2[F:22])[C:6]=1[NH:7][CH3:8].ClC1C=CC=C(C(OO)=[O:41])C=1>C(Cl)(Cl)Cl>[Cl:1][C:2]1[C:3]([O:23][C:24]([F:31])([F:32])[CH:25]([F:30])[C:26]([F:27])([F:28])[F:29])=[N:4][N:5]([C:9]2[CH:14]=[C:13]([S:15]([CH2:16][C:17]([F:20])([F:19])[F:18])=[O:41])[C:12]([CH3:21])=[CH:11][C:10]=2[F:22])[C:6]=1[NH:7][CH3:8]

参加物

4

実験手順

0.24 g of 4-chloro-1-{2-fluoro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl}-3-(1,1,2,3,3,3-hexafluoropropoxy)-5-methylaminopyrazole was dissolved in 10 mL of chloroform, and 120 mg of m-chloroperbenzoic acid (purity: 75%) was added under cooling with ice. After stirring for one hour under cooling with ice, the solution was washed with an aqueous sodium thiosulfate solution and then washed with an aqueous sodium hydrogen carbonate solution, and then dried over anhydrous sodium sulfate. Then, the solvent was distilled off under reduced pressure, and the obtained residue was purified by column chromatography (developing solvent ethyl acetate:hexane=1:2) to obtain 0.24 g of 4-chloro-1-{2-fluoro-4-methyl-5-(2,2,2-trifluoroethylsulfinyl)phenyl}-3-(1,1,2,3,3,3-hexafluoropropoxy)-5-methylaminopyrazole.

後処理

  1. temperatureunder cooling with ice
  2. temperatureunder cooling with ice
  3. washthe solution was washed with an aqueous sodium thiosulfate solution
  4. washwashed with an aqueous sodium hydrogen carbonate solution
  5. dry with materialdried over anhydrous sodium sulfate
  6. distillationThen, the solvent was distilled off under reduced pressure
  7. customthe obtained residue was purified by column chromatography (developing solvent ethyl acetate:hexane=1:2)

出典と根拠

ORDレコード
ord-cecdae981d094af3ba1519500504cfcf
出典データセット
uspto-grants-2014_08
特許番号
US08802713B2

反応ノート

読み込み中…