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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30500Generated: October 29, 2026

Ethanol → Ccpa

https://huagongshe.com/reaction/30500

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 numberUS07423144B2
Source datasetuspto-grants-2008_09
ORD IDord-e91e73d6a5614a31a21e68c1b13e74d7
Source noteuspto-grants-2008_09