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HRID 1290260作成日:2026年10月26日

Indole-3-Butyric Acid → (2,3-Dihydro-benzo[1,4]dioxin-2-ylmethyl)-[4-(1H-indol-3-yl)-butyl]-amine

https://huagongshe.com/reaction/1290260

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1,4-Benzodioxan, 2-(aminomethyl)-, hydrochlorideHCID 2849836—
溶媒DimethylformamideHCID 6228—
生成物(2,3-Dihydro-benzo[1,4]dioxin-2-ylmethyl)-[4-(1H-indol-3-yl)-butyl]-amineHCID 1892388659.4%

反応手順

3-Indolebutyric acid (1.2 g, 6.0 mmole), 1-hydroxybenzotriazole hydrate (0.97 g, 7.2 mmole) and 1,3-diisopropylcarbodiimide (2.3 ml, 14.4 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 2,3-dihydro-1,4-benzodioxin-2methanamine hydrochloride (1.2 g, 6.0 mmole) in 50 ml of DMF and the mixture was further stirred for 24 hours. The solvent was removed and the residue partitioned between dichloromethane and water. The separated dichloromethane 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. Fractions were concentrated and washed with a minimum amount of THF to remove a by-product and to give 1.2 g (57%) of the desired product, (2,3-dihydro-benzo [1,4]dioxin-2-ylmethyl)-4-(1H-indol-3-yl)-butanamide, as an oil.

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-6126f80f08954d2a87a485f198927309
出典メモuspto-grants-1998_05