Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913857Generated: November 1, 2026

Ethanol → Ccpa

https://huagongshe.com/reaction/1913857

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 numberUS08609833B2
Source datasetuspto-grants-2013_12
ORD IDord-4bfe4ffa490b4ff883963fa9a5aef81f
Source noteuspto-grants-2013_12