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HRID 1916808作成日:2026年10月27日

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

https://huagongshe.com/reaction/1916808

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US08618140B2
出典データセットuspto-grants-2013_12
ORD IDord-b8d9497fde23420f91443ef216f526a3
出典メモuspto-grants-2013_12