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HRID 12617作成日:2026年10月26日

Dimethyl Disulfide → ethyl 4-[7-bromo-1-[2-(ethyloxy)-2-oxoethyl]-2-(methylthio)-1H-indol-3-yl]butanoate

https://huagongshe.com/reaction/12617

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl DisulfideHCID 12232—
反応物Sulfuryl chlorideHCID 24648—
反応物Sodium BicarbonateHCID 516892—
反応物ethyl 4-{7-bromo-1-[2-(ethyloxy)-2-oxoethyl]-1H-indol-3-yl}butanoateHCID 66738782—
溶媒ChloroformHCID 6212—
生成物ethyl 4-[7-bromo-1-[2-(ethyloxy)-2-oxoethyl]-2-(methylthio)-1H-indol-3-yl]butanoateHCID 68693460—

反応条件

温度-5 °C

反応手順

To a chloroform (0.8 mL) solution of dimethyl disulfide (30 mg), sulfuryl chloride (34 mg) was added at −15° C. and the mixture was stirred at −5° C. for 1.5 hours. To the reaction mixture, a chloroform (0.5 mL) solution of the compound prepared in Example 43, namely, ethyl 4-{7-bromo-1-[2-(ethyloxy)-2-oxoethyl]-1H-indol-3-yl}butanoate (100 mg) was added at −78° C., followed by stirring at room temperature for 3 hours. To the reaction mixture, an aqueous saturated sodium hydrogen carbonate solution was added under ice cooling, followed by extraction with ethyl acetate. The organic layer was washed in turn with an aqueous saturated sodium hydrogen carbonate solution, water and saturated saline, dried over anhydrous magnesium sulfate and then concentrated. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=95:5→91:9) to obtain the titled compound having the following physical properties (70 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728023B2
出典データセットuspto-grants-2010_06
ORD IDord-89b9fac623f644f58e5b221f3871bc84
出典メモuspto-grants-2010_06