Ammonium Hydroxide → HCID 11035745, compound

HRID 1738299Notes

Reaction equation

HRID 1738299 reaction equation
[F:1][C:2]1[CH:25]=[CH:24][C:5]([C:6]([C:8]2[C:17]([O:18][CH3:19])=[CH:16][CH:15]=[C:14]3[C:9]=2[CH:10]=[CH:11][C:12]([S:20](Cl)(=[O:22])=[O:21])=[CH:13]3)=[O:7])=[CH:4][CH:3]=1.[OH-].[NH4+:27]>O1CCOCC1>[F:1][C:2]1[CH:25]=[CH:24][C:5]([C:6]([C:8]2[C:17]([O:18][CH3:19])=[CH:16][CH:15]=[C:14]3[C:9]=2[CH:10]=[CH:11][C:12]([S:20]([NH2:27])(=[O:22])=[O:21])=[CH:13]3)=[O:7])=[CH:4][CH:3]=1

Participants

4

Procedure

A solution of 5-(4-fluorobenzoyl)-6-methoxy-2-naphthalenesulfonyl chloride (5.39 g, 14.2 mmol), [prepared as described in step 2 above], in dioxane (100 ml), was cooled in an ice bath under nitrogen, and concentrated ammonium hydroxide (20 ml) was added dropwise. After 1h, the dioxane was removed under reduced pressure and the residue was partitioned between water and ethyl acetate. The organic layer was separated and washed with brine, dried over sodium sulfate and concentrated in vacuo. The crude product was purified by flash chromatography (gradient elution, 20-60% ethyl acetate/hexane) and then recrystallized from ethyl acetate/hexane to afford 2.7 g of 5-(4-fluorobenzoyl)-6-methoxy-2-naphthalene-sulfonamide as white crystals.

Workup

  1. customAfter 1h, the dioxane was removed under reduced pressure
  2. customthe residue was partitioned between water and ethyl acetate
  3. customThe organic layer was separated
  4. washwashed with brine
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated in vacuo
  7. customThe crude product was purified by flash chromatography (gradient elution, 20-60% ethyl acetate/hexane)
  8. customrecrystallized from ethyl acetate/hexane

Sources & evidence

ORD record
ord-3516b87bcc934a74b017bcaa4a8eb9f1
Source dataset
uspto-grants-1999_10
Patent number
US05962531

Reaction notes

Loading…