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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49253생성일: 2026년 10월 25일

Ethyl Acetate → 3-{1-[2,3,8,9-Tetrahydrofuro[3,2-f][1,4]benzodioxin-2-ylmethyl]-1,2,3,6-tetrahydro-4-pyridinyl}-1H-indole

https://huagongshe.com/reaction/49253

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물3-(1,2,3,6-Tetrahydropyridin-4-yl)-1H-indoleHCID 2761023—
반응물(2R)-2,3,8,9-tetrahydrofuro[3,2-f][1,4]benzodioxin-2-ylmethyl 4-methylbenzenesulfonateHCID 86586535—
용매Dimethyl SulfoxideHCID 679—
생성물3-{1-[2,3,8,9-Tetrahydrofuro[3,2-f][1,4]benzodioxin-2-ylmethyl]-1,2,3,6-tetrahydro-4-pyridinyl}-1H-indoleHCID 10178355—

반응 단계

A solution of 0.65 g (1.8 mmole) of (2R)-2,3,8,9-tetrahydrofuro[3,2-f][1,4]benzodioxin-2-ylmethyl 4-methylbenzenesulfonate and 1.0 g (5.0 mmole) of 3-(1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole in 10 mL of DMSO was heated under nitrogen at 80° C. for 4 hours. After the reaction had cooled to room temperature, 400 mL of ethyl acetate was added and the solution was washed with 250 mL portions of saturated aqueous sodium bicarbonate, water and saturated brine, dried over sodium sulfate, filtered and concentrated in vacuum. The residue was column chromatographed on silica gel with 2% methanol in chloroform to give 0.32 g of the (S)-enantiomer of the title compound as a gold solid, m.p. 207-209° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706736B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-db03a09d6d574ea78f2d4bc4285fbade
출처 메모uspto-grants-2004_03