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HRID 356955생성일: 2026년 10월 25일

Diisopropylamine → 1-(3-Cyclopentyloxy-4-methoxyphenyl)-2-(3,5-dichloropyrid-4-yl)ethanol

https://huagongshe.com/reaction/356955

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물Ammonium ChlorideHCID 25517—
반응물3-Cyclopentyloxy-4-methoxybenzaldehydeHCID 2735893—
반응물3,5-Dichloro-4-methylpyridineHCID 10953827—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물1-(3-Cyclopentyloxy-4-methoxyphenyl)-2-(3,5-dichloropyrid-4-yl)ethanolHCID 2169768084.9%

반응 단계

A stirred solution of diisopropylamine (9.75 mL) in dry tetrahydrofuran (200 mL) at -70° C. is treated dropwise with a solution of butyl lithium in hexane (27.2 mL; 2.5 M) and the solution is stirred for 30 minutes. It is then treated with a solution of 3,5-dichloro-4-methylpyridine (10.25 g) in dry tetrahydrofuran (60 mL) during 30 minutes, while keeping the temperature below -75° C., and the solution is then stirred for a further 30 minutes. It is then treated with 3- cyclopentyloxy-4-methoxybenzaldehyde (13.92 g) in dry tetrahydrofuran (60 mL) during 15 minutes, and stirred for a further 1 hour 30 minutes at -75° C. The solution is treated with aqueous ammonium chloride solution and extracted with ethyl acetate (3×100 mL). The organic layers are combined, washed with brine, dried and concentrated to low volume. The resulting precipitate is filtered off, to give 1-(3-cyclopentyloxy-4-methoxyphenyl)-2-(3,5-dichloropyrid-4-yl)ethanol (20.5 g), m.p. 124°-125° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05840724
출처 데이터셋uspto-grants-1998_11
ORD IDord-54011e990c764ac6ab6a17024d2ef2ae
출처 메모uspto-grants-1998_11