Ethyl bromopyruvate → HCID 66797364、化合物

HRID 1916884

反応式

HRID 1916884 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9](=[NH:20])[C:10]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=2[F:19])([CH3:12])[CH3:11])=[CH:4][CH:3]=1.C([O-])(O)=O.[Na+].Br[CH2:27][C:28](=O)[C:29]([O:31][CH2:32][CH3:33])=[O:30]>C1COCC1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[CH:27]=[C:28]([C:29]([O:31][CH2:32][CH3:33])=[O:30])[N:20]=[C:9]2[C:10]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=2[F:19])([CH3:12])[CH3:11])=[CH:6][CH:7]=1

参加物

5

反応条件

温度
70 °C

実験手順

To a 250 mL round bottom flask attached with condenser was added N-(4-bromophenyl)-2-(2-fluorophenyl)-2-methylpropanimidamide (5.0 g, 15 mmol), anhydrous THF (80 mL), NaHCO3 (2.52 g, 30 mmol), and 90% ethyl bromopyruvate (1.90 mL, 15.1 mmol). The reaction mixture was stirred at 70° C. for 2 hr prior to analysis by LCMS. The cooled reaction mixture was decanted and concentrated in vacuo. The residue was taken into toluene (65 mL) and acetic acid (1.8 mL). The solution was stirred at reflux for 1 hr. The cooled solution was washed with H2O (150 mL×3), dried over Na2SO4, filtered, concentrated in vacuo, and chromatographed through a SiO2 column using a 100% Hx to 70% EtOAc gradient to afford purified title compound (4.3 g, 67% yield). LCMS (ES): m/z=431.3, 433.3 [M+H]+.

後処理

  1. customTo a 250 mL round bottom flask attached with condenser
  2. customThe cooled reaction mixture
  3. customwas decanted
  4. concentrationconcentrated in vacuo
  5. stirringThe solution was stirred
  6. temperatureat reflux for 1 hr
  7. washThe cooled solution was washed with H2O (150 mL×3)
  8. dry with materialdried over Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo
  11. customchromatographed through a SiO2 column
  12. customto afford

出典と根拠

ORDレコード
ord-264c1cae779945cca665dd7bd7d1dd25
出典データセット
uspto-grants-2013_12
特許番号
US08618154B2

関連ノート

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