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HRID 1057484作成日:2026年10月25日

Acetic Acid → n-((2-Bromo(3-pyridyl))methyl)-2-(1,3-dioxolan-2-yl)ethylamine

https://huagongshe.com/reaction/1057484

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物1,3-Dioxolane-2-ethylamineHCID 79827—
反応物2-BromonicotinaldehydeHCID 4714951—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒1,2-DichloroethaneHCID 11—
生成物n-((2-Bromo(3-pyridyl))methyl)-2-(1,3-dioxolan-2-yl)ethylamineHCID 18671410—

反応手順

To a solution of 2-bromopyridine-3-carbaldehyde (3.53 g, 19.0 mmol, 1.0 eq) (Melnyk et al., Synthetic Commun. 23(19):2727-2730, 1993) in 1,2-dichloroethane (50 mL) was added 2-(1,3-dioxolan-2-yl)ethylamine (TCI-GR, 2.67 g, 22.8 mmol, 1.2 eq), sodium triacetoxyborohydride (Aldrich, 1.61 g, 76 mmol, 4.0 eq) and glacial acetic acid (1.14 g, 19 mmol, 1.0 eq). The reaction mixture was stirred under nitrogen at room temperature for 2 h. The reaction was quenched with 1.0 N aqueous NaOH to about pH 8 and the solution was extracted with EtOAc (200 mL×3). The organic extracts were washed with saturated NaCl, dried with MgSO4, filtered and concentrated. Flash column chromatography (silica gel, 0-10% EtOAc-Hexane) afforded the title compound as a colorless oil. MS m/z 377 (Br=79, M+H), 379 (Br=81, M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06514964B1
出典データセットuspto-grants-2003_02
ORD IDord-1a0522ab9a454381afebffe8fe1e703b
出典メモuspto-grants-2003_02