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HRID 715910作成日:2026年10月26日

Dimethyl Disulfide → 2-Chloro-5-(methylthio)pyrimidine

https://huagongshe.com/reaction/715910

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Ammonium ChlorideHCID 25517—
反応物5-Bromo-2-chloropyrimidineHCID 606665—
反応物HCID 178418244HCID 178418244—
溶媒TetrahydrofuranHCID 8028—
生成物2-Chloro-5-(methylthio)pyrimidineHCID 2197953218%

反応手順

A solution of 1.00 g (5.17 mmol) of 5-bromo-2-chloropyrimidine and 551 μl (6.20 mmol) of dimethyl disulfide in 26 ml of tetrahydrofuran was cooled to −78° C. and 1.89 ml (5.17 mmol) of 2.73 N n-butyl lithium/n-hexane solution was added thereto, and the reaction solution was stirred for 2 hours. After completion of the reaction, saturated ammonium chloride aqueous solution was added to the reaction solution and the reaction solution was extracted with ethyl acetate. The organic layer was washed with saturated sodium chloride aqueous solution and dried with anhydrous sodium sulfate, and then the solvent was distilled off under reduced pressure. The obtained residue was subjected to silica gel column chromatography [n-hexane/ethyl acetate=90/10 (V/V)] and the fraction including the desired compound was concentrated under reduced pressure to provide 149 mg of the title compound as a white solid (yield: 18%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09187450B2
出典データセットuspto-grants-2015_11
ORD IDord-796ea8d6c4474d02b1083efd32a43173
出典メモuspto-grants-2015_11