Sulfuric Acid → 3-Amino-6-chloro-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide

HRID 516910Notes

Reaction equation

HRID 516910 reaction equation
[CH3:1][O:2][N:3]([CH3:21])[S:4]([C:7]1[C:15]2[O:14]C(C(C)(C)C)=[N:12][C:11]=2[CH:10]=[CH:9][C:8]=1[Cl:20])(=[O:6])=[O:5].S(=O)(=O)(O)O>O1CCOCC1.O>[NH2:12][C:11]1[C:15]([OH:14])=[C:7]([S:4]([N:3]([O:2][CH3:1])[CH3:21])(=[O:6])=[O:5])[C:8]([Cl:20])=[CH:9][CH:10]=1

Participants

5

Procedure

2-tert-Butyl-6-chloro-benzooxazole-7-sulfonic acid methoxy-methyl-amide (4.8 g, 14.42 mmol) in dioxane (55 ml) and water (20 ml) was treated with concentrated sulphuric acid (20 ml) added dropwise over 30 minutes maintaining the temperature <30° C. The reaction mixture was heated at reflux for 2.5 h and then allowed to cool to RT. Dioxane was removed in vacuo and the resulting aqueous residue was basified with sat. NaHCO3 solution (250 ml) to pH12. The reaction mixture was extracted with EtOAc (3×200 ml) and the combined organic extracts were washed with water (3×100 ml) sat. brine (100 ml), dried (MgSO4) and concentrated in vacuo to afford the title compound as a brown solid; [M+H]+ 266.

Workup

  1. additionadded dropwise over 30 minutes
  2. temperaturemaintaining the temperature <30° C
  3. temperatureThe reaction mixture was heated
  4. temperatureat reflux for 2.5 h
  5. customDioxane was removed in vacuo
  6. extractionThe reaction mixture was extracted with EtOAc (3×200 ml)
  7. washthe combined organic extracts were washed with water (3×100 ml) sat. brine (100 ml)
  8. dry with materialdried (MgSO4)
  9. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-33e9a3d55dea4b85a4ed3f107bc26a98
Source dataset
uspto-grants-2015_08
Patent number
US09115087B2

Reaction notes

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