HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanethiol → 2'-Deoxy-2'-methylthio-5-methyluridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanethiol | HCID 878 | — |
| Reactant | 1,1,3,3-Tetramethylguanidine | HCID 66460 | — |
| Reactant | 2,2'-Anhydro-1-beta-arabinofuranosylthymine | HCID 168045 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2'-Deoxy-2'-methylthio-5-methyluridine | HCID 10334293 | 74.1% |
Reaction Steps
2.2′-Anhydro-5-methyluridine (17.02 g, 70.6 mmol), methanethiol (16.3 g, 339 mmol), 1,1,3,3-tetramethylguanidine (40.6 g, 353 mmol), and dimethylformamide (150 ml) were heated together at 60° C. After 12 hr, the products were cooled and concentrated under reduced pressure. The residual oil was purified by short silica gel (300 g) column chromatography. Concentration of appropriate fractions, which were eluted with CH2Cl2-MeOH (93:7, v/v), furnished the title compound as a white foam (15.08 g, 74.1%). Crystallization from EtOH-CH2Cl2 furnished white needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06307040B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-6b367e86d8654ac4a8f7118bd2a4d660 |
| Source note | uspto-grants-2001_10 |