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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382483Generated: October 31, 2026

Sodium hydride → HCID 66630814, compound

https://huagongshe.com/reaction/2382483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactantp-Chlorophenethylic alcoholHCID 74647—
ReactantHCID 86647566HCID 86647566—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66630814HCID 66630814—

Reaction Conditions

Temperature50 °C

Reaction Steps

The title compound is prepared by adding N-{(3aR,4S,6R,6aS)-6-[2-Chloro-6-(2,2-diphenyl-ethylamino)-purin-9-yl]-2,2-dimethyl-tetrahydro-cyclopenta[1,3]dioxol-4-yl}-propionamide (example 235, step 1) to a premixed solution of sodium hydride (60% in oil) and 2-(4-chloro-phenyl)-ethanol (1 equivalent) in dry THF. The reaction is stirred at 50° C. for 48 hours, before quenching residual sodium hydride with excess aqueous ammonium chloride. The reaction mixture id then partitioned between ethyl acetate and water; the organic phase is washed consecutively with water and brine before drying over magnesium sulfate. Filtration and removal of the volatile components under reduced pressure yields the crude product; purification by column chromatography/crystallisation affords the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258141B2
Source datasetuspto-grants-2012_09
ORD IDord-959e549406b04c8694c19bafea170953
Source noteuspto-grants-2012_09