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HRID 460145作成日:2026年10月26日

Acetic Acid → (6,4'-Dimethoxybiphenyl-3-ylmethyl)-(1-quinolin-4-yl-ethyl)-amine

https://huagongshe.com/reaction/460145

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Sodium cyanoborohydrideHCID 5003444—
反応物1-(Quinolin-4-yl)ethan-1-amineHCID 10844927—
反応物6,4'-Dimethoxybiphenyl-3-carbaldehydeHCID 22391191—
溶媒MethanolHCID 887—
生成物(6,4'-Dimethoxybiphenyl-3-ylmethyl)-(1-quinolin-4-yl-ethyl)-amineHCID 2239133772%

反応手順

The 1-quinolin-4-yl-ethylamine (510 mg, 3 mmol) and 6,4′-dimethoxy-biphenyl-3-carbaldehyde (242 mg, 1.0 mmol) were stirred with acetic acid (300 mg, J. T. Baker) in methyl alcohol (15 mL0 at room temperature for 4 h. To the reaction solution was added sodium cyanoborohydride (1.0 g, 16 mmol, Aldrich) at 0° C. The mixture was stirred under nitrogen at room temperature for overnight then the reaction was cooled at ice bath and quenched with saturated aqueous sodium bicarbonate (30 mL). The methyl alcohol was removed from the mixture via vacuo. The residue was extracted by ethyl acetate (30 mL×4). The combined organic phases were dried over anhydrous magnesium sulfate and concentrated via vacuo. The title compound was purified by column chromatography (silica gel, ethyl acetate) in form as white solid in 72% yield (287 mg, 0.72 mmol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07196102B2
出典データセットuspto-grants-2007_03
ORD IDord-e31bc11dfb4b474c8aec9a14c75911e6
出典メモuspto-grants-2007_03