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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1290262생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1290262

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylcarbodiimideHCID 12734—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물1,4-Benzodioxan, 2-(aminomethyl)-, hydrochlorideHCID 2849836—
반응물4-(5-Fluoro-1H-indol-3-yl)butanoic acidHCID 15047268—
용매DimethylformamideHCID 6228—
생성물(2,3-Dihydro-benzo[1,4]dioxin-2-ylmethyl)-[4-(5-fluoro-1H-indol-3-yl)-butyl]-amineHCID 1892389762.2%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05750724
출처 데이터셋uspto-grants-1998_05
ORD IDord-b751c17837eb4944b4c7098d9437aded
출처 메모uspto-grants-1998_05