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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215731Generated: October 27, 2026

Oxygen → 1-[5-O-Benzoyl-2-deoxy-4-ethynyl-3-O-methanesulfonyl-beta-D-threo-pentofuranosyl]thymine

https://huagongshe.com/reaction/215731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilyl triflateHCID 65367—
Reactant1-[5-O-Benzoyl-2-deoxy-4-ethynyl-beta-D-threo-pentofuranosyl]thymineHCID 11588761—
Catalystpalladium(II) acetateHCID 167845—
Product1-[5-O-Benzoyl-2-deoxy-4-ethynyl-3-O-methanesulfonyl-beta-D-threo-pentofuranosyl]thymineHCID 8663921988%

Reaction Steps

To a stirring mixture of 4 (3.58 g, 8.72 mmol) and Et3N (6.1 ml, 43.6 mmol) was added Me3SiOSO2CF3 (2.56 mL, 13.0 mmol) at 0° C. under positive pressure of dry Ar. The mixture was stirred for 30 min at the same temperature, and then partitioned between CH2Cl2 and sat. aqueous NaHCO3. The organic layer was dried (Na2SO4) and evaporated. The residue was dissolved in DMSO (12 mL). To this solution was added Pd(OAc)2 (98 mg, 0.44 mmol), and the mixture was stirred for 36 h under positive pressure of O2. The mixture was partitioned between EtOAc and brine. The organic layer was dried (Na2SO4), evaporated, and chromatographed on a silica gel column (hexane/EtOAc=5/1) to give 5 (3.13 g, 88%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193165B2
Source datasetuspto-grants-2012_06
ORD IDord-0e9360100908407eb80e35bfbcc30902
Source noteuspto-grants-2012_06