3-phenyl-5-(4-methyl-beta-hydroxyphenethyl)-N-methyl-isoxazole-4-carboxamide → N-methyl-5-(4-methylphenacyl)-3-phenyl-4-isoxazole carboxamide

HRID 2083787ノート

反応式

HRID 2083787 の反応式
[C:1]1([C:7]2[C:11]([C:12]([NH:14][CH3:15])=[O:13])=[C:10]([CH2:16][CH:17]([OH:25])[C:18]3[CH:23]=[CH:22][C:21]([CH3:24])=[CH:20][CH:19]=3)[O:9][N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CC(C)=O.OS(O)(=O)=O.O=[Cr](=O)=O>CC(C)=O>[CH3:15][NH:14][C:12]([C:11]1[C:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)=[N:8][O:9][C:10]=1[CH2:16][C:17]([C:18]1[CH:23]=[CH:22][C:21]([CH3:24])=[CH:20][CH:19]=1)=[O:25])=[O:13]

参加物

4

実験手順

A mixture of 41.4 g. (0.123 mole) of 3-phenyl-5-(4-methyl-β-hydroxyphenethyl)-N-methyl-isoxazole-4-carboxamide and 800 ml. of acetone is treated dropwise with the addition of 92.5 ml. (0.185 mole) of Jones reagent [100 g. chromium trioxide, 160 ml. concentrated sulfuric acid with water to 500 ml.] and the resulting mixture is stirred at room temperature for 2 hours. The supernatant liquid is decanted and the solvent removed in vacuo, the residue is taken up in water/methylene chloride and the layers separated. The organic phase is washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo. The residue is treated with ether to give a solid and then triturated with ethanol to give N-methyl-5-(4-methylphenacyl)-3-phenyl-4-isoxazole carboxamide.

後処理

  1. additionA mixture of 41.4 g
  2. customThe supernatant liquid is decanted
  3. customthe solvent removed in vacuo
  4. customthe layers separated
  5. washThe organic phase is washed with saturated sodium chloride solution
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. customevaporated in vacuo
  9. additionThe residue is treated with ether
  10. customto give a solid
  11. customtriturated with ethanol

出典と根拠

ORDレコード
ord-734a3875c2ab49a99454de18223f5b00
出典データセット
uspto-grants-1978_04
特許番号
US04086421

反応ノート

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