돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 374212생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/374212

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물DiisopropylethylamineHCID 81531—
반응물2H-1-Benzopyran-2-one, 7-(3-chloropropoxy)-HCID 1900666—
반응물2,3-Dihydro-7-hydroxy-1,4-benzodioxin-2-methanamineHCID 18923891—
반응물Isopropanol hydrochlorideHCID 21912024—
용매MethanolHCID 887—
용매IsopropanolHCID 3776—
용매DimethylformamideHCID 6228—
생성물7-[3-[[(2,3-Dihydro-7-hydroxy-1,4-benzodioxin-2-yl)methyl]amino]propoxy]-2H-1-benzopyran-2-oneHCID 1977866516%

반응 단계

2,3-Dihydro-7-hydroxy-1,4-benzodioxin-2-methanamine (3.00 g, 16.6 mmole), 7-(3-chloropropoxy)coumarin (2.95 g, 12.4 mmole), diisopropylethylamine (8.0 ml, 46.0 mmole) and sodium iodide (2.58 g, 17.2 mmole) were combined in 150 ml of DMF and heated at 80°-100° C. for 2 days under a nitrogen atmosphere. The solvent was then removed and replaced with dichloromethane. The mixture was washed with an equal volume of saturated aqueous sodium bicarbonate, with saturated aqueous sodium chloride, dried over magnesium sulfate, filtered, and concentrated in vacuum. The residue was column chromatographed on silica gel using first dichloromethane and then 0.25% methanol/dichloromethane as eluant. The product-containing fractions were combined and concentrated in vacuum and the pure free base (1.0 g, an additional 2.0 g were obtained of lower purity) redissolved in methanol and boiled on a hot plate, the methanol gradually being replaced with isopropanol. 4N HCl/IPA was added and the title compound was collected by filtration and dried in vacuum at 80° C. The procedure yielded 0.76 g of beige solid, monohydrochloride, m.p. 252° C. (d).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05166367
출처 데이터셋uspto-grants-1992_11
ORD IDord-37ea97c2bcb44e0db0b441e64c640a41
출처 메모uspto-grants-1992_11