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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Methylimidazole | HCID 12749 | — |
| Reactant | 3-[(Dimethylamino)Methyl]-4-Oxo-2,3,4,9-Tetrahydrothiopyrano[2,3-b]Indole | HCID 19826153 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[(2-Methyl-1-Imidazolyl)Methyl]-4-Oxo-2,3,4,9-Tetrahydrothiopyrano[2,3-b]Indole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05030646 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-210aaedc075d4159888d164a6f6cdbb3 |
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| Source note | uspto-grants-1991_07 |
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