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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1176335생성일: 2026년 10월 26일

Sodium hydride → tert-Butyl 3-{2-[3-(2-acetylaminoethyl)indol-1-yl]ethoxy}-4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidine-1-carboxylate

https://huagongshe.com/reaction/1176335

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물N-AcetyltryptamineHCID 70547—
반응물Sodium BicarbonateHCID 516892—
반응물Tert-butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-[2-(toluene-4-sulphonyloxy)ethoxy]piperidine-1-carboxylateHCID 86609984—
용매DimethylformamideHCID 6228—
생성물tert-Butyl 3-{2-[3-(2-acetylaminoethyl)indol-1-yl]ethoxy}-4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidine-1-carboxylateHCID 68501498—

반응 단계

A suspension of 0.20 g of tert-butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-[2-(toluene-4-sulphonyloxy)ethoxy]piperidine-1-carboxylate (Example 14b) and 0.067 g of N-[2-(1H-indol-3-yl)ethyl]acetamide in 7 ml of N,N-dimethylformamide is admixed at 0° C. with 0.024 g of sodium hydride dispersion (60%) and stirred at room temperature over 20 hours. The reaction mixture is poured onto saturated aqueous sodium bicarbonate solution and extracted with ethyl acetate (2×). The combined organic phases are washed with brine, dried over sodium sulphate and concentrated by evaporation. The title compound is obtained as a yellow oil from the residue by means of flash chromatography (SiO2 60F). Rf=0.35 (EtOAc); Rt=5.69.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07842688B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-0fb41553436545509cd2e817fed0846f
출처 메모uspto-grants-2010_11