Reaktion #59885

Reaktionsgleichung

sodium hydrogen carbonate

toluene

2-(((4-(5,9-dioxaspiro[3.5]non-7-yloxy)-3-methylpyridin-2-yl)methyl)thio)-1H-benzimidazole

3-chloroperbenzoic acid

→

title compound

Ausbeute 76.2%

2-(((4-(5,9-dioxaspiro[3.5]non-7-yloxy)-3-methylpyridin-2-yl)methyl)sulfinyl)-1H-benzimidazole

Ausbeute 76.2%

Lösungsmittel

methanol

toluene methanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONwas added at −70° C. in a nitrogen atmosphere
2. 2
   TemperaturAfter the mixture was warmed to room temperature
3. 3
   Extraktionthe mixture was extracted with ethyl acetate twice
4. 4
   Trocknendried over anhydrous sodium sulfate
5. 5
   Filtrationfiltered
6. 6
   Einengenconcentrated
7. 7
   SonstigeThe residue was purified by silica gel column chromatography (NH silica gel, elution solvent: ethyl acetate, ethyl acetate/methanol=9/1)
8. 8
   workup.ADDITIONFractions containing the title compound
9. 9
   Sonstigewas collected by use of ethyl acetate
10. 10
    Einengenconcentrated
11. 11
    workup.ADDITIONAfter diethyl ether was added to the residue
12. 12
    workup.DISTILLATIONthe solvent was distilled off

Vorschrift

To a toluene (30 ml)/methanol (3 ml) solution of the 2-(((4-(5,9-dioxaspiro[3.5]non-7-yloxy)-3-methylpyridin-2-yl)methyl)thio)-1H-benzimidazole (290 mg, 0.73 mmol) obtained in the step (9h), a toluene/methanol (10:1) solution of 3-chloroperbenzoic acid (174 mg, 0.65 mmol as the content was regarded as 65%) was added at −70° C. in a nitrogen atmosphere. After the mixture was stirred at −50° C. for one hour, a saturated aqueous solution of sodium hydrogen carbonate was added. After the mixture was warmed to room temperature, the mixture was extracted with ethyl acetate twice. Organic layers were combined and dried over anhydrous sodium sulfate, filtered and concentrated. The residue was purified by silica gel column chromatography (NH silica gel, elution solvent: ethyl acetate, ethyl acetate/methanol=9/1). Fractions containing the title compound was collected by use of ethyl acetate and concentrated. After diethyl ether was added to the residue, the solvent was distilled off to obtain the title compound (230 mg, yield: 76.2%) as a white solid.

Quelle