Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492475Generated: November 2, 2026

Phosphate → HCID 14258065, compound

https://huagongshe.com/reaction/1492475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
ReactantLithium hydrideHCID 62714—
Reactant6-(2-Methoxyethoxy)-7H-purin-2-amineHCID 13546809—
ReactantHCID 15280201HCID 15280201—
SolventDimethylformamideHCID 6228—
ProductHCID 14258065HCID 1425806597.5%

Reaction Steps

In an atmosphere of argon gas, lithium hydride (4.8 mg, 0.6 mmole) was added to a suspension of 2-amino-6-(2-methoxyethoxy)-purine (354.4 mg, 1.69 mmoles) in anhydrous DMF (15 ml). After stirring the mixture at room temperature for one hour, (3S,4S)-3,4-bis(benzoyloxymethyl)-7-oxabicyclo[4.1.0]-heptane (310.4 mg, 0.85 mmole) was added, and the reaction was further continued at 140° C. for 1.5 hours. Then, while cooling the reaction mixture, 0.2M phosphate buffer solution (pH 7.0) was added thereto and the mixture was stirred for a while, and then the mixture was subjected to extraction with ethyl acetate. The extract solution was washed with water, washed with saturated aqueous solution of sodium chloride and dried on anhydrous sodium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to obtain 2-amino-9-[1R,2R,4S,5S)-4,5-bis(benzoyloxymethyl)-2-hydroxycyclohexyl]-6-(2-methoxyethoxy)-purine (320 mg, Yield 65.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05374625
Source datasetuspto-grants-1994_12
ORD IDord-9ce804154ff7454d934ac38b9dc9831b
Source noteuspto-grants-1994_12