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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 374215생성일: 2026년 10월 26일

Sodium Iodide → 7-[3-[[(2,3-Dihydro-7-methoxy-1,4-benzodioxin-2-yl)methyl]amino]propoxy]-2H-1-benzopyran-2-one

https://huagongshe.com/reaction/374215

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물DiisopropylethylamineHCID 81531—
반응물2H-1-Benzopyran-2-one, 7-(3-chloropropoxy)-HCID 1900666—
반응물(7-Methoxy-2,3-dihydro-1,4-benzodioxin-2-YL)methanamineHCID 18923874—
용매DimethylformamideHCID 6228—
생성물7-[3-[[(2,3-Dihydro-7-methoxy-1,4-benzodioxin-2-yl)methyl]amino]propoxy]-2H-1-benzopyran-2-oneHCID 1977866840.3%

반응 조건

온도100 °C

반응 단계

2,3-Dihydro-7-methoxy-1,4-benzodioxin-2-methanamine (3.8 g, 20 mmole), 7-(3-chloropropoxy)coumarin (4.8 g, 20 mmole), diisopropylethylamine (2.6 g, 20 mmole) and sodium iodide (5.0 g, 33 mmole) were combined in 200 ml of DMF and heated at 100° C. for 24 hours under a nitrogen atmosphere. The solvent was then removed and replaced with 500 ml of dichloromethane. The mixture was washed with 300 ml portions of saturated aqueous sodium bicarbonate, with saturated aqueous sodium chloride, dried over sodium sulfate, filtered, and concentrated in vacuum. The residue was column chromatographed on 100 g of silica gel using first dichloromethane, then chloroform, and finally 2% methanol in chloroform as eluant. The product-containing fractions were combined and concentrated in vacuum and the residue crystallized from 100 ml of isopropanol with the addition of 5.0 ml of 4N isopropanolic HCl to give 3.2 g of title compound as a white solid, monohydrochloride, m.p. 223°- 225° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05166367
출처 데이터셋uspto-grants-1992_11
ORD IDord-0fedae0cffc44585965de7dad80c3cb4
출처 메모uspto-grants-1992_11