HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379290Generated: October 31, 2026
Methanethiol → 2'-Deoxy-2'-methylthiouridine
https://huagongshe.com/reaction/1379290
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanethiol | HCID 878 | — |
| Reactant | 1,1,3,3-Tetramethylguanidine | HCID 66460 | — |
| Reactant | 2,2'-Anhydrouridine | HCID 806138 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2'-Deoxy-2'-methylthiouridine | HCID 131720208 | 80.1% |
Reaction Steps
2,2'-Anhydrouridine (15.5 g, 68.2 mmol) [Rao, T. S. and Reese, C. B. (1989) J. Chem. Soc., Chem. Commun., 997], methanethiol (15.7 g, 327 mmol), 1,1,3,3-tetramethylguanidine (39.2 g, 341 mmol) and dimethylforamide (150 ml), were heated together at 60° C. After 12 hr, the reaction mixture was cooled and concentrated under reduced pressure. The residual oil was purified by flash column chromatography on silica gel (300 g). Concentration of the appropriate, fractions, which were eluted with CH2Cl2 -MeOH (9:1, v/v), and drying of the residue under high vacuum gave 2'-deoxy-2'-methylthiouridine as a pale yellow solid (14.11 g, 75.4%). Attempts to crystallize the solids from ethanol-hexanes (as reported by Imazawa, M., Ueda, T., and Ukita, T. (1975) Chem. Pharm. Bull., 23:604) failed and the material turned into a hygroscopic foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05670633 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-e7d379517a6a4287ba607ecaeeb35423 |
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| Source note | uspto-grants-1997_09 |
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