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HRID 1290249作成日:2026年10月26日

Indole-3-Butyric Acid → [4-(1H-Indol-3-yl)-butyl]-(7-methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)amine

https://huagongshe.com/reaction/1290249

反応式

関与物質

役割名称HCID仕込み量
反応物Indole-3-Butyric AcidHCID 8617—
反応物DiisopropylcarbodiimideHCID 12734—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
反応物(S)-7-methoxy-2,3-dihydro-1,4-benzodioxin-2-methanamine hydrochlorideHCID 70200787—
溶媒DimethylformamideHCID 6228—
生成物[4-(1H-Indol-3-yl)-butyl]-(7-methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)amineHCID 1892389863%

反応手順

3-Indolebutyric acid (1.3 g, 6.5 mmole), 1-hydroxybenzotriazole hydrate (1.1 g, 7.8 mmole) and 1,3-diisopropylcarbodiimide (2.4 ml, 15.6 mmole) were combined in 100 ml of DMF and stirred at room temperature for 2 hours under a nitrogen atmosphere. To this was added dropwise (S)-7-methoxy-2,3-dihydro-1,4-benzodioxin-2-methanamine hydrochloride (1.5 g, 6.5 mmole) in 50 ml of DMF and the mixture was further stirred for 24 hours. The solvent was removed and replaced with dichloromethane. The mixture was then washed with H2O. The separated organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuum. The residue was chromatographed on a silica gel column using ethyl acetate as the eluant. Evaporation of product fractions gave 1.5 g (61%) of the desired product, (S)-(7-methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-4-(1H-indol-3-yl)-butanamide, as a foam.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05750724
出典データセットuspto-grants-1998_05
ORD IDord-79d3293c36994725a9b2649cf472b858
出典メモuspto-grants-1998_05