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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790813Generated: October 30, 2026

Dicyclohexylcarbodiimide → 2',3'-dideoxy-3'-fluoro-5'-O-[5-(N-trityl-L-valyloxymethyl)-6-stearoyloxyhexanoyl]guanosine

https://huagongshe.com/reaction/1790813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant5-(N-trityl-L-valyloxymethyl)-6-stearoyloxyhexanoic acidHCID 15485173—
Reactant3'-Fluoro-2',3'-dideoxyguanosineHCID 135431817—
SolventDimethylformamideHCID 6228—
Product2',3'-dideoxy-3'-fluoro-5'-O-[5-(N-trityl-L-valyloxymethyl)-6-stearoyloxyhexanoyl]guanosineHCID 136121706—

Reaction Steps

To a solution of 5-(N-trityl-L-valyloxymethyl)-6-stearoyloxyhexanoic acid (462 mg, 0.6 mmole) and 2′,3′-dideoxy-3′-fluoroguanosine (340 mg, 1.25 mmol) in DMF (3 ml) were added dimethylaminopyridine (7 mg, 0.06 mmole), and DCC (136 mg, 0.66 mmol). The reaction was kept at room temperature overnight, and then at 40° C. for two hours. The reaction mixture was filtered through Celite and poured into dichloromethane, and washed with aqueous sodium hydrogen carbonate solution. The product 2′,3′-dideoxy-3′-fluoro-5′-O-[5-(N-trityl-L-valyloxymethyl)-6-stearoyloxyhexanoyl) guanosine was isolated by silica gel column chromatography. (93 mg)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071173B2
Source datasetuspto-grants-2006_07
ORD IDord-2a1842918cfe48009ac4bd036a2c86d6
Source noteuspto-grants-2006_07