Bromine → HCID 86644708、化合物

HRID 1097531ノート

反応式

HRID 1097531 の反応式
[NH2:1][C:2]1[CH:29]=[CH:28][C:5]([O:6][C:7]2[CH:8]=[CH:9][C:10]([F:27])=[C:11]([NH:13][C:14](=[O:26])[CH2:15][C:16]3[CH:21]=[CH:20][CH:19]=[C:18]([C:22]([F:25])([F:24])[F:23])[CH:17]=3)[CH:12]=2)=[C:4]([C:30]#[N:31])[CH:3]=1.[S-:32][C:33]#[N:34].[K+].BrBr>C(O)(=O)C>[NH2:34][C:33]1[S:32][C:3]2[C:4]([C:30]#[N:31])=[C:5]([O:6][C:7]3[CH:8]=[CH:9][C:10]([F:27])=[C:11]([NH:13][C:14](=[O:26])[CH2:15][C:16]4[CH:21]=[CH:20][CH:19]=[C:18]([C:22]([F:23])([F:24])[F:25])[CH:17]=4)[CH:12]=3)[CH:28]=[CH:29][C:2]=2[N:1]=1

参加物

5

実験手順

To a solution of N-[5-(4-amino-2-cyanophenoxy)-2-fluorophenyl]-2-[3-(trifluoromethyl)phenyl]acetamide (1.15 g, 2.68 mmol) in acetic acid (40 mL) was added potassium thiocyanate (1.22 g, 12.6 mmol), and the mixture was stirred at room temperature for 10 min. A solution of bromine (652 mg, 4.08 mmol) in acetic acid (6.5 mL) was added dropwise to the obtained solution over 10 min. After the completion of the dropwise addition, the mixture was stirred at room temperature for 12 hr. The reaction mixture was diluted with acetic acid (50 mL), and insoluble material was filtered off and washed with acetic acid, the filtrate and washings were combined and the mixture was concentrated under reduced pressure. The obtained residue was suspended in ethyl acetate (120 mL)/tetrahydrofuran (12 mL), and the suspension was washed successively with saturated aqueous sodium hydrogen carbonate solution (120 mL) and saturated brine (120 mL), and dried over anhydrous magnesium sulfate. Insoluble material was filtered off, the filtrate was purified by basic silica gel column chromatography (eluate: ethyl acetate), and the obtained solution was concentrated under reduced pressure to give the title compound (1.13 g, 87%) as a beige powder.

後処理

  1. additionAfter the completion of the dropwise addition
  2. stirringthe mixture was stirred at room temperature for 12 hr
  3. filtrationwas filtered off
  4. washwashed with acetic acid
  5. concentrationthe mixture was concentrated under reduced pressure
  6. washthe suspension was washed successively with saturated aqueous sodium hydrogen carbonate solution (120 mL) and saturated brine (120 mL)
  7. dry with materialdried over anhydrous magnesium sulfate
  8. filtrationInsoluble material was filtered off
  9. customthe filtrate was purified by basic silica gel column chromatography (eluate: ethyl acetate)
  10. concentrationthe obtained solution was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-bb56f762c6954947b6ed7582cd236b08
出典データセット
uspto-grants-2012_03
特許番号
US08143258B2

反応ノート

読み込み中…