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HRID 49255作成日:2026年10月25日

Ethyl Acetate → 3-{1-[2,3-Dihydrofuro[3,2-f][1,4]benzodioxin-2-ylmethyl]-1,2,3,6-tetrahydropyridin-4-yl}-1H-indole

https://huagongshe.com/reaction/49255

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物3-(1,2,3,6-Tetrahydropyridin-4-yl)-1H-indoleHCID 2761023—
反応物(2R)-2,3-dihydrofuro[3,2-f][1,4]benzodioxin-2-ylmethyl 4-methylbenzenesulfonateHCID 11439815—
溶媒Dimethyl SulfoxideHCID 679—
生成物3-{1-[2,3-Dihydrofuro[3,2-f][1,4]benzodioxin-2-ylmethyl]-1,2,3,6-tetrahydropyridin-4-yl}-1H-indoleHCID 9930070—

反応手順

A solution of 0.40 g (1.1 mmole) of (2R)-2,3-dihydrofuro[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 0.27 g of the (S)-enantiomer of the title compound as a white solid, m.p. 208-209° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06706736B2
出典データセットuspto-grants-2004_03
ORD IDord-276e64281b7c4ca98250d148688195c5
出典メモuspto-grants-2004_03