N,N-二甲基甲酰胺 → 3-Amino-4-(4-hydroxy-phenylsulfanyl)-benzoic acid methyl ester

HRID 607222笔记

反应方程式

HRID 607222 反应方程式
[CH3:1][O:2][C:3](=[O:21])[C:4]1[CH:9]=[CH:8][C:7]([S:10][C:11]2[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=2)=[C:6]([N+:18]([O-])=O)[CH:5]=1.CN(C=O)C.[Cl-].[NH4+]>O1CCCC1.O.C(O)C.[Fe]>[CH3:1][O:2][C:3](=[O:21])[C:4]1[CH:9]=[CH:8][C:7]([S:10][C:11]2[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=2)=[C:6]([NH2:18])[CH:5]=1

参与物

8

实验过程

A suspension of the product of Example 113A (as a mono DMF adduct)(7.25 g, 19.23 mmol) ammonium chloride (1.54 g, 28.8 mmol) and iron powder (5.37 g, 96.15 mmol) in tetrahydrofuran (75 mL), water (25 mL) and ethanol (75 mL) was heated at reflux for 3 hours. The reaction was cooled to room temperature, and the mixture was filtered through a pad of celite, which was then washed with methanol, and the filtrate concentrated to a solid under vacuum. The residue was then dissolved in water (100 mL) and extracted with dichloromethane (2×50 mL). The combined organic extracts were washed with brine (25 mL), dried over magnesium sulfate, filtered, and concentrated under vacuum to provide the title compound as a white solid (4.2 g, 79%).

后处理

  1. temperaturewas heated
  2. temperatureat reflux for 3 hours
  3. filtrationthe mixture was filtered through a pad of celite, which
  4. washwas then washed with methanol
  5. concentrationthe filtrate concentrated to a solid under vacuum
  6. dissolutionThe residue was then dissolved in water (100 mL)
  7. extractionextracted with dichloromethane (2×50 mL)
  8. washThe combined organic extracts were washed with brine (25 mL)
  9. dry with materialdried over magnesium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated under vacuum

来源与证据

ORD记录
ord-b639d4c3969040dd94deebb7615f6577
来源数据集
uspto-grants-2011_03
专利号
US07915411B2

反应笔记

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