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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260156Generated: November 1, 2026

Ethanol → N6-Cyclopentyladenosine

https://huagongshe.com/reaction/1260156

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 organic 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 numberUS08470800B2
Source datasetuspto-grants-2013_06
ORD IDord-784bf357a6c84acba5e64e6f2843422c
Source noteuspto-grants-2013_06