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HRID 872409作成日:2026年10月26日

Sodium borohydride → 1-(2-Aminopyridin-4-yl)ethanol

https://huagongshe.com/reaction/872409

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium borohydrideHCID 4311764—
反応物1-(2-Aminopyridin-4-yl)ethan-1-oneHCID 13145258—
溶媒MethanolHCID 887—
生成物1-(2-Aminopyridin-4-yl)ethanolHCID 1799914845.2%

反応手順

To a mixture of 1-(2-aminopyridin-4-yl)ethanone (21) (168 mg, 1.234 mmol) in MeOH (10 mL), under nitrogen at 0° C., was added sodium borohydride (46.7 mg, 1.234 mmol). The resulting reaction mixture was stirred at RT for 2 hr, and then the solvents were removed under reduced pressure. The residue was taken up into EtOAc (25 mL), and extracted with saturated aq NaHCO3 solution (30 mL) and the layers separated. The aqueous layer was extracted with EtOAc (20 mL×2), and the combined organic extracts were washed with brine (30 mL), dried and the solvents removed under reduced pressure, to give 1-(2-aminopyridin-4-yl)ethanol (22) (77 mg, 45%) as a yellow oil: m/z 139 (M+H)+ (ES+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08975285B2
出典データセットuspto-grants-2015_03
ORD IDord-b0ee208866054cd0bebe63a8c6e36b21
出典メモuspto-grants-2015_03