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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489061Generated: October 30, 2026

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

https://huagongshe.com/reaction/489061

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 numberUS06974802B2
Source datasetuspto-grants-2005_12
ORD IDord-672802043d1e4b84998b9eb86a00c148
Source noteuspto-grants-2005_12