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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374223Generated: November 2, 2026

Iodoethane → HCID 53682906, compound

https://huagongshe.com/reaction/374223

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantDiisopropylethylamineHCID 81531—
Reactant(S)-7-[3-[[(2,3-Dihydro-6,7-methylenedioxy-1,4-benzodioxin-2-yl)methyl]amino]propoxy]-2H-1-benzopyran-2-one hydrochlorideHCID 86746374—
SolventDimethylformamideHCID 6228—
ProductHCID 53682906HCID 5368290643.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

(S)-7-[3-[[(2,3-Dihydro-6,7-methylenedioxy-1,4-benzodioxin-2-yl)methyl]amino]propoxy]-2H-1-benzopyran-2-one hydrochloride (0.60 g, 1.3 mmole), iodoethane (0.16 ml, 2.0 mmole) and diisopropylethylamine (2.26 ml, 13.0 mmole) were combined in 50 ml of DMF and heated at 60° C. for 2 days under a nitrogen atmosphere. The solvent was then removed in vacuum and the residue was dissolved in dichloromethane and washed with an equal volume of aqueous saturated sodium bicarbonate. The aqueous portion was back-extracted with dichloromethane and the combined organic portions were washed with water, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was chromatographed on a silica gel column using dichloromethane as eluant. The product-containing fractions 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. The mixture was diluted with isopropanol to precipitate a white solid, which was recrystallized from methanol to give 0.25 g of the title compound as the monohydrochloride, m.p. 209° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166367
Source datasetuspto-grants-1992_11
ORD IDord-7e21ffc617b44d77be76df3710948a19
Source noteuspto-grants-1992_11