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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086517Generated: November 1, 2026

Methyl iodide → 3-[(2-Methyl-1-Imidazolyl)Methyl]-4-Oxo-2,3,4,9-Tetrahydrothiopyrano[2,3-b]Indole

https://huagongshe.com/reaction/1086517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium CarbonateHCID 10340—
Reactant2-MethylimidazoleHCID 12749—
Reactant3-[(Dimethylamino)Methyl]-4-Oxo-2,3,4,9-Tetrahydrothiopyrano[2,3-b]IndoleHCID 19826153—
SolventDimethylformamideHCID 6228—
Product3-[(2-Methyl-1-Imidazolyl)Methyl]-4-Oxo-2,3,4,9-Tetrahydrothiopyrano[2,3-b]IndoleHCID 19826156—

Reaction Steps

5.60 ml (0.09 mol) of iodomethane are added to a solution of 23.43 g (0.09 mol) of 3-[(dimethylamino)methyl]-4-oxo-2,3,4,9-tetrahydrothiopyrano[2,3-b]indole (hydrochloride) in 250 ml of dimethylformamide. The mixture is stirred at room temperature for 1 hour, a solution of 22.17 g (0.27 mol) of 2-methylimidazole in 50 ml of dimethylformamide is then added and the reaction medium is thereafter heated to 100° C. for 36 hours. After the mixture is cooled, 500 ml of 2N aqueous sodium carbonate solution are added and the resulting mixture is extracted three times with ethyl acetate. The organic phases are combined, washed with water (200 ml), dried and concentrated under vacuum. The product is chromatographed on silica, eluting with a methylene chloride/ethanol/ammonia solution mixture (92:8:0.5). The residue is recrystallized in acetonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05030646
Source datasetuspto-grants-1991_07
ORD IDord-210aaedc075d4159888d164a6f6cdbb3
Source noteuspto-grants-1991_07