HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325067Generated: October 25, 2026
Methyl iodide → 2'-O-methyl-5-methyl-2thiouridine
https://huagongshe.com/reaction/325067
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Dibutyltin oxide | HCID 61221 | — |
| Reactant | 5-Methyl-2-thiouridine | HCID 6915711 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2'-O-methyl-5-methyl-2thiouridine | HCID 18660585 | — |
Reaction Steps
To a stirred solution of 5-methyl-2-thiouridine (0.500 g, 1.8 mmol) in DMF (10 ml) is added dibutyltin oxide (0.500 g, 2.0 mmol), tetrabutyl ammonium iodide (0.738 g, 2 mmol), and methyl iodide (1.022 g, 7.2 mmol). The reaction flask is sealed and heated at 50° C. for 16 hours. The mixture is cooled and another portion of methyl iodide is added (1.022 g, 7.2 mmol) and the reaction heated for an additional 16 hours. At the end of this time, the reaction mixture is cooled to room temperature and diluted with methylene chloride and chromatographed using a methylene chloride/methanol gradient. The appropriate fractions are collected and concentrated to give 2′-O-methyl-5-methyl-2-thiouridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06222025B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-98474743a3b34e30a6df5cadec096d9f |
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| Source note | uspto-grants-2001_04 |
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