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HRID 930926作成日:2026年10月27日

Iodoethane → 3-Bromo-2-chloro-5-(ethylsulfonyl)pyridine

https://huagongshe.com/reaction/930926

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物Sodium SulfiteHCID 24437—
反応物Sodium BicarbonateHCID 516892—
反応物5-Bromo-6-chloropyridine-3-sulfonyl chlorideHCID 2793626—
溶媒WaterHCID 962—
生成物3-Bromo-2-chloro-5-(ethylsulfonyl)pyridineHCID 59326565—

反応条件

温度75 °C

反応手順

Sodium sulfite (1.755 g, 13.92 mmol) and sodium bicarbonate (1.231 g, 14.65 mmol) were dissolved in water (37 mL) to give a colorless solution. The mixture was heated at 75° C. 3-Bromo-2-chloropyridine-5-sulfonyl chloride (2.132 g, 7.33 mmol) was added portionwise over 1 hour. The reaction mixture was stirred at 75° C. for 1 hour. The mixture was concentrated and N,N-dimethylformamide (13.88 mL) was added. Sodium bicarbonate (1.231 g, 14.65 mmol) and iodoethane (0.589 mL, 7.33 mmol) were added. The resulting mixture was heated to 75° C. for 2 hours and then cooled to ambient temperature. The mixture was partitioned between ethyl acetate and water. The organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated. The residue was purified by flash chromatography (silica gel, 0-100% ethyl acetate/heptane) to provide the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09296741B2
出典データセットuspto-grants-2016_03
ORD IDord-84952ea5e3604f048e593a31dd7ee4df
出典メモuspto-grants-2016_03