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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31607생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/31607

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참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물m-Chloroperbenzoic acidHCID 70297—
반응물Sodium BicarbonateHCID 516892—
반응물2-(((4-(5,9-dioxaspiro[3.5]non-7-yloxy)-3-methylpyridin-2-yl)methyl)thio)-1H-benzimidazoleHCID 59792469—
용매MethanolHCID 887—
용매Toluene methanolHCID 21867641—
생성물2-(((4-(5,9-dioxaspiro[3.5]non-7-yloxy)-3-methylpyridin-2-yl)methyl)sulfinyl)-1H-benzimidazoleHCID 1200312176.2%

반응 조건

온도-50 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425634B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-9d7d5cdcaaa943238a9ce57c1f8a1516
출처 메모uspto-grants-2008_09