Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082467Generated: October 28, 2026

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

https://huagongshe.com/reaction/2082467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantDiisopropylethylamineHCID 81531—
Reactant2H-1-Benzopyran-2-one, 7-(3-chloropropoxy)-HCID 1900666—
ReactantN-Ethyl-2,3-dihydro-7-hydroxy-1,4-benzodioxin-2-methanamineHCID 19778687—
SolventDimethylformamideHCID 6228—
Product7-[3-[[(2,3-Dihydro-7-hydroxy-1,4-benzodioxin-2-yl)methyl]ethylamino]propoxy]-2H-1-benzopyran-2-oneHCID 1977866413.5%

Reaction Conditions

Temperature94 °C

Reaction Steps

N-Ethyl-2,3-dihydro-7-hydroxy-1,4-benzodioxin-2-methanamine (2.11 g, 13.1 mmole), 7-(3-chloropropoxy)coumarin (3.44 g, 14.4 mmole), diisopropylethylamine (11 ml, 63.2 mmole) and sodium iodide (1.98 g, 13.2 mmole) were combined in 175 ml of DMF and heated at 94° C. for 2 days under a nitrogen atmosphere. The solvent was then removed in vacuum and the residue column chromatographed on silica gel using first 0.5% methanol/dichloromethane and then 1.5% methanol/dichloromethane as eluant. The product-containing fractions were combined and concentrated in vacuum and the residue redissolved in dichloromethane and boiled on a hot plate, the dichloromethane gradually being replaced with isopropanol. 4N HCl/isopropanol (4 ml) was added and the title compound was collected by filtration. A second recrystallization from isopropanol yielded 0.73 g of white solid, monohydrochloride, m.p. 208°-215° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05189171
Source datasetuspto-grants-1993_02
ORD IDord-0b2d4ea816b947609d6a4297e9ec3c87
Source noteuspto-grants-1993_02