Hydrochloric Acid → 4-hydroxy-N-[4-(methylsulfonyl)-1,3-thiazol-2-yl]benzamide

HRID 1644766ノート

反応式

HRID 1644766 の反応式
Cl.C([O:5][C:6]1[CH:11]=[CH:10][C:9]([C:12](=[O:23])[NH:13][C:14]2[S:15][CH:16]=[C:17]([S:19]([CH3:22])(=[O:21])=[O:20])[N:18]=2)=[CH:8][CH:7]=1)(=O)C>O1CCCC1>[OH:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]([NH:13][C:14]2[S:15][CH:16]=[C:17]([S:19]([CH3:22])(=[O:21])=[O:20])[N:18]=2)=[O:23])=[CH:8][CH:7]=1

参加物

4

実験手順

2 M hydrochloric acid (3.0 mL) was added to a suspension of 83 (0.12 g, 0.35 mmol) in tetrahydrofuran (3.0 mL), and the resulting suspension was warmed to reflux. The reaction became homogeneous upon heating. After refluxing for 1.5 h, the reaction was allowed to cool to room temperature, and then partitioned between diethyl ether and water. The ether layer was washed with water, saturated aqueous sodium bicarbonate, and brine. The ether layer was dried with anhydrous sodium sulfate and concentrated in vacuo. The residue triturated with ethyl acetate, the solvent was removed under a stream of nitrogen, and the resulting solid was dried in vacuo at 55° C. to give 84 (0.086 g, 82%) as a light yellow solid.

後処理

  1. temperaturethe resulting suspension was warmed to reflux
  2. temperatureupon heating
  3. temperatureAfter refluxing for 1.5 h
  4. custompartitioned between diethyl ether and water
  5. washThe ether layer was washed with water, saturated aqueous sodium bicarbonate, and brine
  6. dry with materialThe ether layer was dried with anhydrous sodium sulfate
  7. concentrationconcentrated in vacuo
  8. customThe residue triturated with ethyl acetate
  9. customthe solvent was removed under a stream of nitrogen
  10. customthe resulting solid was dried in vacuo at 55° C.

出典と根拠

ORDレコード
ord-2942c9a9dc6f414a9b53fb1842c84ce9
出典データセット
uspto-grants-2012_02
特許番号
US08124632B2

反応ノート

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