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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 460145생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/460145

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물1-(Quinolin-4-yl)ethan-1-amineHCID 10844927—
반응물6,4'-Dimethoxybiphenyl-3-carbaldehydeHCID 22391191—
용매MethanolHCID 887—
생성물(6,4'-Dimethoxybiphenyl-3-ylmethyl)-(1-quinolin-4-yl-ethyl)-amineHCID 2239133772%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07196102B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-e31bc11dfb4b474c8aec9a14c75911e6
출처 메모uspto-grants-2007_03