Sodium Thiosulfate → 1H-Imidazole, 5-((3,5-dimethylphenyl)sulfonyl)-1,2-dimethyl-4-(1-methylethyl)-

HRID 1416041Notes

Reaction equation

HRID 1416041 reaction equation
CC1C=C(S[C:10]2[N:14]([CH3:15])[C:13]([CH3:16])=[N:12][C:11]=2[CH:17]([CH3:19])[CH3:18])C=C(C)C=1.Cl[C:21]1[CH:26]=[CH:25][CH:24]=[C:23]([C:27](OO)=O)[CH:22]=1.[S:31]([O-:35])([O-])(=[O:33])=S.[Na+].[Na+].[C:38](=O)([O-])O.[Na+]>C(Cl)Cl>[CH3:38][C:21]1[CH:26]=[C:25]([S:31]([C:10]2[N:14]([CH3:15])[C:13]([CH3:16])=[N:12][C:11]=2[CH:17]([CH3:18])[CH3:19])(=[O:35])=[O:33])[CH:24]=[C:23]([CH3:27])[CH:22]=1

Participants

6

Procedure

In methylene chloride (6 ml)was dissolved 60 mg (0.20 mmol)of 5-(3,5-dimethylphenylthio)-4-isopropyl-1,2-dimethyl-1H-imidazole, followed by addition of 223 mg (1.00 mmol)of 80% metachloroperbenzoic acid, and the mixture was stirred at room temperature for 1 hour. To the reaction mixture, an aqueous solution of sodium thiosulfate and then an aqueous solution of sodium hydrogen carbonate were added, and the mixture was extracted with methylene chloride. The extract was washed with saturated brine and dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure. The residue purified by silica gel chromatography (ethyl acetate), and recrystallized from n-hexane, to give 24 mg of Compound I-105 (yield 39%), mp 126-128° C.

Workup

  1. extractionthe mixture was extracted with methylene chloride
  2. washThe extract was washed with saturated brine
  3. dry with materialdried over anhydrous sodium sulfate
  4. filtrationfiltered
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. customThe residue purified by silica gel chromatography (ethyl acetate)
  7. customrecrystallized from n-hexane

Sources & evidence

ORD record
ord-35dc1bb70308466eb94b458fdecaf235
Source dataset
uspto-grants-1999_06
Patent number
US05910506

Reaction notes

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