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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082456Generated: November 2, 2026

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

https://huagongshe.com/reaction/2082456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant2-Aminomethyl-1,4-benzodioxaneHCID 15053—
ReactantDiisopropylethylamineHCID 81531—
Reactant2H-1-Benzopyran-2-one, 7-(3-chloropropoxy)-HCID 1900666—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product7-[3-[[(2,3-Dihydro-1,4-benzodioxin-2-yl)methyl]amino]propoxy]-2H-1-benzopyran-2-oneHCID 988554929.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

2,3-Dihydro-1,4-benzodioxin-2-methanamine (1.7 g, 10 mmole), 7-(3-chloropropoxy)coumarin (2.4 g, 10 mmole), diisopropylethylamine (1.3 g, 10 mmole) and sodium iodide (5.0 g, 33 mmole) were combined in 100 ml of N-methylpyrrolidinone and heated at 80° C. for 24 hours under a nitrogen atmosphere. The solvent was then removed and replaced with 300 ml of dichloromethane. The mixture was washed with an equal volume 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 chloroform as eluant. The product-containing fractions (Rf=0.15 on silica gel tlc with 1% methanol/chloroform) were combined and concentrated in vacuum and the residue crystallized from isopropanol with the addition of 4N isopropanolic HCl to give 1.1 g of title compound as a tan solid, monohydrochloride, m.p. 213°-215° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05189171
Source datasetuspto-grants-1993_02
ORD IDord-371ee7030c2b4f9eb45a23f66e86883c
Source noteuspto-grants-1993_02