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HRID 17112作成日:2026年10月24日

Methanol → 1-(6-Bromopyridin-2-yl)propan-1-amine

https://huagongshe.com/ja/reaction/17112

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Pyridine-2-carbonitrileHCID 7522—
反応物TetrahydrofuranHCID 8028—
反応物Sodium borohydrideHCID 4311764—
反応物HCID 178418443HCID 178418443—
生成物1-(6-Bromopyridin-2-yl)propan-1-amineHCID 60133734—

反応条件

温度0 °C

反応手順

Ethyl magnesium bromide (3.0 mL, 3.0 mmol) was added dropwise over 10 min to a solution of the pyridine nitrile A466.2 (500 mg, 2.75 mmol) in THF (5 mL) at room temperature under a nitrogen atmosphere. After strring for 30 min at room temperature, the reaction mixture was then cooled to 0° C. and anhydrous methanol added (2.75 mL) followed by sodium borohydride (15 mg, 3.0 mmol). The mixture was allowed to warm to room temperature over 1 hr before quenching with saturated ammonium chloride solution (10 mL) and stirring overnight at room temperature. The mixture was diluted with water (20 mL) and extracted with ethyl acetate (3×30 mL). The combined organics were dried (MgSO4), evaporated in vacuo and purified by column chromatography using 10% MeOH in ethyl acetate as eluant to yield A466.3 (237 mg). HPLC YMC S-5 4.6×33 mm (2 min grad): retention time 0.87 min, M+H+=217.15

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737279B2
出典データセットuspto-grants-2010_06
ORD IDord-0458abe1459e4a29bb6e52b8dc8bbbed
出典メモuspto-grants-2010_06