1-[[1-(2-Methylsulfanylethyl)benzimidazol-2-yl]methyl]benzotriazole → 1-[[1-(2-Methylsulfonylethyl)benzimidazol-2-yl]methyl]benzotriazole

HRID 1796120Notes

Reaction equation

HRID 1796120 reaction equation
[CH3:1][S:2][CH2:3][CH2:4][N:5]1[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[N:7]=[C:6]1[CH2:14][N:15]1[C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=2[N:17]=[N:16]1.[OH2:24].[OH2:25].O.O.O.O.C1(=O)OOOOC(=O)C2=CC=CC=C12.[Mg]>CN(C)C=O.CCOC(C)=O>[CH3:1][S:2]([CH2:3][CH2:4][N:5]1[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[N:7]=[C:6]1[CH2:14][N:15]1[C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=2[N:17]=[N:16]1)(=[O:25])=[O:24]

Participants

5

Procedure

1-[1-(2-Methylthio-ethyl)-1H-benzimidazol-2-ylmethyl]-1H-benzotriazole (100 mg, 0.309 mmol) was dissolved in anhydrous N,N-dimethylformamide (5 mL). Magnesium monoperoxy phthalate hexahydrate (611 mg, 1.24 mmol) was added and the reaction mixture was stirred at room temperature overnight under N2. The solvent was stripped under reduced pressure. The yellow oily residue was taken up in EtOAc (100 mL) and washed with water (2×50 mL) dried over magnesium sulfate, filtered and evaporated. Column chromatography on silica gel (EtOAc) gave 45 mg (41%) of the title compound as an oil.

Workup

  1. washwashed with water (2×50 mL)
  2. dry with materialdried over magnesium sulfate
  3. filtrationfiltered
  4. customevaporated

Sources & evidence

ORD record
ord-a138bb9ba5f6417ab80a6186e5590175
Source dataset
uspto-grants-2006_04
Patent number
US07030140B2

Reaction notes

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