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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2082459생성일: 2026년 10월 27일

Sodium Iodide → 7-[3-[[(2,3-Dihydro-6-phenylmethoxy-1,4-benzodioxin-2-yl)methyl]amino]propoxy]-2H-1-benzopyran-2-one

https://huagongshe.com/reaction/2082459

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물DiisopropylethylamineHCID 81531—
반응물2H-1-Benzopyran-2-one, 7-(3-chloropropoxy)-HCID 1900666—
반응물2,3-Dihydro-6-benzyloxy-1,4-benzodioxin-2-methanamineHCID 19778680—
용매DimethylformamideHCID 6228—
생성물7-[3-[[(2,3-Dihydro-6-phenylmethoxy-1,4-benzodioxin-2-yl)methyl]amino]propoxy]-2H-1-benzopyran-2-oneHCID 19778675—

반응 조건

온도108 °C

반응 단계

2,3-Dihydro-6-benzyloxy-1,4-benzodioxin-2-methanamine (2.4 g, 8.85 mmole), 7-(3-chloropropoxy)coumarin (2.15 g, 9.0 mmole), diisopropylethylamine (7.0 ml, 40.2 mmole) and sodium iodide (1.35 g, 9.0 mmole) were combined in 200 ml of DMF and heated at 108° 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 water dried over magnesium sulfate, filtered, and concentrated in vacuum. The residue was column chromatographed on silica gel using 1% methanol/dichloromethane as eluant. The product-containing fractions (Rf=0.27 on silica gel tlc with 2.5% methanol/dichloromethane) were combined and concentrated in vacuum and the residue redissolved in dichloromethane and boiled on a hot plate, the solvent gradually being replaced with isopropanol. Upon addition of 6 ml of 4N HCl/isopropanol and cooling, 1.22 g of the title compound, m.p. 184°-187° C., precipitated as a beige solid, monohydrochloride.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05189171
출처 데이터셋uspto-grants-1993_02
ORD IDord-0d1e7fe96ba2490e871d6f69400b2fa7
출처 메모uspto-grants-1993_02