Pyridine → 4-[4-(Benzenesulfonylamino)-phenyl]-butyric acid

HRID 1198192

反応式

HRID 1198192 の反応式
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][CH2:10][C:11]([OH:13])=[O:12])=[CH:4][CH:3]=1.[C:14]1([S:20](Cl)(=[O:22])=[O:21])[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.N1C=CC=CC=1>CC(C)=O>[C:14]1([S:20]([NH:1][C:2]2[CH:3]=[CH:4][C:5]([CH2:8][CH2:9][CH2:10][C:11]([OH:13])=[O:12])=[CH:6][CH:7]=2)(=[O:22])=[O:21])[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1

参加物

5

実験手順

To a solution of 4-(4-aminophenyl)butyric acid (1 g, 5.6 mmol) in dry acetone (30 ml) was added dropwise a solution of benzenesulphonyl chloride (0.99 g) and pyridine (1.1 g) in dry acetone (10 ml). The mixture was heated at reflux for 3 hours, then concentrated in vacuo. The resulting oil was dissolved in dichloromethane (100 ml) and the solution was washed with 2N aqueous HCl (2×100 ml), followed by water (2×100 ml). The dichloromethane solution was extracted with 10% aqueous NaOH (2×50 ml), followed by water (2×50 ml), and these extracts were combined and stirred with dichloromethane (100 ml) while conc. HCl was added to adjust the pH of the mixture to 5. The layers were separated and the organic solution was dried (MgSO04) and concentrated in vacuo. The resulting solid was recrystallised from isopropanol to give 4-[4-(phenyl-sulphonamido)phenyl]butyric acid. (1.03 g, 58%) mp. 128°-130 ° C.

後処理

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 3 hours
  3. concentrationconcentrated in vacuo
  4. dissolutionThe resulting oil was dissolved in dichloromethane (100 ml)
  5. washthe solution was washed with 2N aqueous HCl (2×100 ml)
  6. extractionThe dichloromethane solution was extracted with 10% aqueous NaOH (2×50 ml)
  7. additionwas added
  8. customThe layers were separated
  9. customthe organic solution was dried (MgSO04)
  10. concentrationconcentrated in vacuo
  11. customThe resulting solid was recrystallised from isopropanol

出典と根拠

ORDレコード
ord-203b9b6dc5f64056803659a99d88da05
出典データセット
uspto-grants-1994_01
特許番号
US05280043

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