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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379290Generated: October 31, 2026

Methanethiol → 2'-Deoxy-2'-methylthiouridine

https://huagongshe.com/reaction/1379290

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, 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05670633
Source datasetuspto-grants-1997_09
ORD IDord-e7d379517a6a4287ba607ecaeeb35423
Source noteuspto-grants-1997_09