Potassium Carbonate → HCID 86744603、化合物

HRID 981465

反応式

HRID 981465 の反応式
[SH:1][CH2:2][C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:4].[C:11](=[O:14])([O-])[O-].[K+].[K+].CO[C:19]1[CH:24]=[CH:23][C:22]([CH:25]2[O:27][CH:26]2[C:28]([NH2:30])=[O:29])=[CH:21][CH:20]=1>C(#N)C>[OH:27][CH:26]([CH:25]([S:1][CH2:2][C:3](=[O:4])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)[C:22]1[CH:23]=[CH:24][CH:19]=[CH:20][C:21]=1[C:5]1[CH:10]=[CH:9][C:8]([O:14][CH3:11])=[CH:7][CH:6]=1)[C:28]([NH2:30])=[O:29]

参加物

5

実験手順

To a solution of 8.0 g (0.052 mol) of 2-mercapto-1-phenylethanone in 120 mL of acetonitrile was added 0.3 g (0.052 mol) of powdered potassium carbonate and 10.1 g (0.052 mol) of 3-(4-methoxyphenyl)oxiranecarboxamide. After the mixture was stirred and heated at reflux under nitrogen for 3.5 hours the solvent was removed under reduced pressure. The crude product was chromatographed on silica gel (150 g). The column was eluted with ethyl acetate, fractions 7-13 containing the product were combined and the solvent was removed under reduced pressure. The residue was crystallized from ethyl acetate to give 4.0 g (22%) of rac.-(R,*R*)-α-hydroxy-4-methoxyphenyl- β-[(2-oxo-2 -phenylethyl)thio]benzenepropanamide, mp 132°-134°.

後処理

  1. temperatureheated
  2. temperatureat reflux under nitrogen for 3.5 hours the solvent
  3. customwas removed under reduced pressure
  4. customThe crude product was chromatographed on silica gel (150 g)
  5. washThe column was eluted with ethyl acetate, fractions 7-13 containing the product
  6. customthe solvent was removed under reduced pressure
  7. customThe residue was crystallized from ethyl acetate

出典と根拠

ORDレコード
ord-ca016424f88d4acdba6b9945f017e20a
出典データセット
uspto-grants-1991_02
特許番号
US04992432

関連ノート

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