HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612839Generated: October 29, 2026
Methanethiol → 2'-Deoxy-2'-methylthiouridine
https://huagongshe.com/reaction/612839
Participants
| Role | Name | HCID | Charge |
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| 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 and Reese, J. Chem. Soc., Chem. Commun., 997], methanethiol (15.7 g, 327 mmol), 1,1,3,3-tetramethylguanidine (39.2 g, 341 mmol) and DMF (150 mL) were heated at 60° C. After 12 hours, 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), and drying the residue under reduced pressure gave 2'-deoxy-2'-methylthiouridine as a pale yellow solid (14.11 g, 75.4%). Attempts to crystallize the solids from EtOH-hexanes [as reported by Imazawa et al., Chem. Pharm. Bull., 23, 604 (1975)] failed and the material turned into a hygroscopic foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06005087 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-ac71f4fd6d2e4e7baac5a2f13f31273c |
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| Source note | uspto-grants-1999_12 |
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