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HRID 1290262作成日:2026年10月27日

Diisopropylcarbodiimide → (2,3-Dihydro-benzo[1,4]dioxin-2-ylmethyl)-[4-(5-fluoro-1H-indol-3-yl)-butyl]-amine

https://huagongshe.com/reaction/1290262

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylcarbodiimideHCID 12734—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
反応物1,4-Benzodioxan, 2-(aminomethyl)-, hydrochlorideHCID 2849836—
反応物4-(5-Fluoro-1H-indol-3-yl)butanoic acidHCID 15047268—
溶媒DimethylformamideHCID 6228—
生成物(2,3-Dihydro-benzo[1,4]dioxin-2-ylmethyl)-[4-(5-fluoro-1H-indol-3-yl)-butyl]-amineHCID 1892389762.2%

反応手順

5-Fluoroindole-3-butyric acid (1.5 g, 6.8 mmole), 1-hydroxybenzotriazole hydrate (1.1 g, 8.2 mmole) and 1,3-diisopropylcarbodiimide (2.6 ml, 16.3 mmole) were combined in 150 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-2-methanamine hydrochloride (1.4 g, 6.8 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 of the products were concentrated and washed with a minimum amount of THF to remove a by-product and to give 1.5 g (60%) of the desired product, (2,3-dihydrobenzo[1,4]dioxin-2-ylmethyl)-4-(5-fluoro-1H-indole-3yl)-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-b751c17837eb4944b4c7098d9437aded
出典メモuspto-grants-1998_05