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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374222Generated: October 30, 2026

Sodium Iodide → HCID 54110178, compound

https://huagongshe.com/reaction/374222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant2H-1-Benzopyran-2-one, 7-(3-chloropropoxy)-HCID 1900666—
ReactantHCID 67796344HCID 67796344—
SolventDimethylformamideHCID 6228—
ProductHCID 54110178HCID 5411017816.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

(S)-2,3-Dihydro-6,7-methylenedioxy-1,4-benzodioxin-2-methanamine hydrochloride (5.50 g, 22.4 mmole), 7-(3-chloropropoxy)coumarin (5.49 g, 23.0 mmole) diisopropylethylamine (39.0 ml, 224 mmol) and sodium iodide (3.45 g, 23.0 mmole) were combined in 200 ml of DMF and heated at 80° C. for 24 hours under a nitrogen atmosphere. The solvent was then removed in vacuum and replaced with chloroform. The mixture was treated with an equal volume of saturated aqueous sodium bicarbonate and the aqueous phase was then back-extracted with 3:1 chloroform-isopropanol. The combined organic extracts were washed with water, dried over anhydrous magnesium sulfate, filtered and concentrated under vacuum. The residue was chromatographed on a silica gel column using dichloromethane as eluant. The product-containing fractions (Rf=0.59 on silica gel tlc with 1:5:95 ammonium hydroxide-methanol-chloroform) were combined and concentrated in vacuum, and the residue redissolved in methanol and acidified with 4N HCl/isopropanol to pH<3 in an ice bath to precipitate a white solid. This was recrystallized from methanol and triturated with a small amount of isopropanol to give 1.50 g of the title compound as an off-white crystalline, solid, monohydrochloride, m.p. 244°-245° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166367
Source datasetuspto-grants-1992_11
ORD IDord-118f4b9630b74b388f7db15521eeaa44
Source noteuspto-grants-1992_11