Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492471Generated: October 31, 2026

Adenine → HCID 67823190, compound

https://huagongshe.com/reaction/1492471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAdenineHCID 190—
ReactantPhosphateHCID 1061—
ReactantSodium hydrideHCID 24758—
ReactantHCID 15280201HCID 15280201—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 67823190HCID 6782319048%

Reaction Steps

In an atmosphere of argon gas, 60% sodium hydride (20 mg, 0.65 mole) was added to a suspension of adenine (202.5 mg, 1.34 mmoles) in anhydrous DMF (10 ml). After stirring the mixture at room temperature for one hour, (3S,4S)-3,4-bis(benzoyloxymethyl)-7-oxabicyclo-[4.1.0]heptane (245 mg, 0.67 mmole) was added and the resulting mixture was heated in an oil bath kept at 140° C. for 3 hours. After adding 0.2M phosphate buffer (pH 7.0) to the reaction mixture and stirring the mixture for a while, the mixture was subjected to extraction with ethyl acetate. After drying the extract solution on anhydrous sodium sulfate, the solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (methylene chloride:methanol=50:1, v/v) to obtain 9-[(1R,2R,4S,5S)-4,5-bis(benzoyloxymethyl)-2-hydroxycyclohexyl]-adenine (161 mg, Yield 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05374625
Source datasetuspto-grants-1994_12
ORD IDord-73336e9fc4404977b11249c3cd543c26
Source noteuspto-grants-1994_12