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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260157Generated: November 1, 2026

Ethanol → Ccpa

https://huagongshe.com/reaction/1260157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantCyclopentylamineHCID 2906—
ReactantHCID 68406760HCID 68406760—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductCcpaHCID 123807—

Reaction Steps

2′,3′,5′-triacetoxy-2,6-dichloroadenosine (1.5 g) and cyclopentylamine (8 eq.) were diluted with ethanol (50 eq.) and the resulting solution was heated at reflux for about 15 hours, then cooled to room temperature and concentrated in vacuo to provide a crude residue which was diluted with a mixture of ethyl acetate and water and transferred to a separatory funnel. The organic layer was separated, dried over sodium sulfate and concentrated in vacuo to provide a crude residue which was purified using flash column chromatography on silica gel (8% MeOH-dichloromethane as eluent) to provide 2-chloro-N6-cyclopentyladenosine (0.948 g). MS m/z 370.32 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470800B2
Source datasetuspto-grants-2013_06
ORD IDord-8a0c2795373c4bfd9d32e39c588c80b7
Source noteuspto-grants-2013_06