4-Methoxybenzenesulfonyl chloride → HCID 18626203, compound

HRID 1859728Notes

Reaction equation

HRID 1859728 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([S:9](Cl)(=[O:11])=[O:10])=[CH:5][CH:4]=1.[NH2:13][C:14]1[CH:15]=[C:16]([CH:26]=[CH:27][C:28]=1[O:29][CH3:30])[C:17]([NH:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)=[O:18]>N1C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([NH:13][C:14]2[CH:15]=[C:16]([CH:26]=[CH:27][C:28]=2[O:29][CH3:30])[C:17]([NH:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[O:18])(=[O:11])=[O:10])=[CH:5][CH:4]=1

Participants

4

Procedure

A mixture of 4-methoxybenzenesulfonyl chloride (2.21 g, 10.0 mmol), 3-amino-4-methoxy-N-phenyl-benzamide (2.43 g, 10.0 mmol) and pyridine (25 mL) was allowed to stand at room temperature until thin layer chromatography indicated the reaction to be complete. The mixture was then partitioned between water (400 mL) and ethyl acetate (400 mL). The layers were separated and the organic layer washed with water (2×400 mL), 1N HCL (100 mL), and brine (100 mL), dried (magnesium sulfate), filtered and stripped of solvent. Trituration of the residue in hexanes/ethyl acetate (1:1) and filtration afforded the product (3.754 g); m.p. 184-186° C.

Workup

  1. customto stand at room temperature until thin layer chromatography
  2. customthe reaction
  3. customThe mixture was then partitioned between water (400 mL) and ethyl acetate (400 mL)
  4. customThe layers were separated
  5. washthe organic layer washed with water (2×400 mL), 1N HCL (100 mL), and brine (100 mL)
  6. dry with materialdried (magnesium sulfate)
  7. filtrationfiltered
  8. filtrationTrituration of the residue in hexanes/ethyl acetate (1:1) and filtration

Sources & evidence

ORD record
ord-ab9f1fa6c88a43f4854fbd76351c1eb2
Source dataset
uspto-grants-2003_03
Patent number
US06528528B2

Reaction notes

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