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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30501Generated: October 30, 2026

Ethanol → N6-Cyclopentyladenosine

https://huagongshe.com/reaction/30501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantCyclopentylamineHCID 2906—
Reactant6-ChloroadenosineHCID 66601553—
SolventMethanolHCID 887—
ProductN6-CyclopentyladenosineHCID 657378—

Reaction Steps

A solution of 6-chloroadenosine (43 g) and cyclopentylamine (5 eq.) in ethanol (50 eq.) was heated at reflux for 3 hours then cooled to room temperature. The resultant reaction mixture was concentrated in vacuo and the resultant residue was diluted with water (400 ml) and ethyl acetate (400 ml). The eoganic layer was separated and the aqueous layer was extracted into ethyl acetate (2×400 ml). The combined organic layers were washed with water (2×200 ml), dried over sodium sulfate, concentrated in vacuo and dried under vacuum to provide a solid which was suspended in MeOH (400 mL), filtered and dried to provide N6-cyclopentyladenosine (43.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423144B2
Source datasetuspto-grants-2008_09
ORD IDord-76e3fc0a7431444e9249f4953bb3d5a8
Source noteuspto-grants-2008_09