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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363244Generated: October 30, 2026

Methanethiol → 2'-Deoxy-2'-methylthiouridine

https://huagongshe.com/reaction/363244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanethiolHCID 878—
Reactant1,1,3,3-TetramethylguanidineHCID 66460—
Reactant2,2'-AnhydrouridineHCID 806138—
SolventDimethylformamideHCID 6228—
Product2'-Deoxy-2'-methylthiouridineHCID 13172020880.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05872232
Source datasetuspto-grants-1999_02
ORD IDord-3ea1d849bd114e5c8c4e8dd672c5bf5a
Source noteuspto-grants-1999_02