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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082475Generated: October 27, 2026

N-Ethyl-2,3-dihydro-1,4-benzodioxin-2-methanamine → 7-[3-[[(2,3-Dihydro-1,4-benzodioxin-2-yl)methyl]ethylamino]propoxy]-2H-1-benzopyran-2-one

https://huagongshe.com/reaction/2082475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Ethyl-2,3-dihydro-1,4-benzodioxin-2-methanamineHCID 30614—
ReactantDiisopropylethylamineHCID 81531—
Reactant7-(3-bromopropoxy)-2H-chromen-2-oneHCID 2757176—
SolventDimethylformamideHCID 6228—
Product7-[3-[[(2,3-Dihydro-1,4-benzodioxin-2-yl)methyl]ethylamino]propoxy]-2H-1-benzopyran-2-oneHCID 1977868451.6%

Reaction Conditions

Temperature76 °C

Reaction Steps

N-Ethyl-2,3-dihydro-1,4-benzodioxin-2-methanamine (4.67 g, 24.2 mmole), 7-(3-bromopropoxy)coumarin (6.92 g, 24.4 mmole), and diisopropylethylamine (6.70 ml, 38.5 mmole) were combined in 300 ml of DMF and heated at 76° C. for 24 hours under a nitrogen atmosphere. The solvent was then removed in vacuum and replaced with dichloromethane. The mixture was washed with an equal volume of saturated aqueous sodium bicarbonate, dried over magnesium sulfate, filtered and concentrated in vacuum. The residue (10 g) was column chromatographed on 225 g of silica gel using 40% ethyl acetate/dichloromethane as eluant. The product-containing fractions were concentrated in vacuum and the residue crystallized from isopropanol with the addition of 30 ml of 4N isopropanolic HCl to give 4.94 g of the title compound as a white solid, monohydrochloride, m.p. 147°-152° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05189171
Source datasetuspto-grants-1993_02
ORD IDord-7155d65dfa884794ae690469367ca06c
Source noteuspto-grants-1993_02