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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703770Generated: November 1, 2026

Cyclopentylamine → HCID 15051904, compound

https://huagongshe.com/reaction/703770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentylamineHCID 2906—
ReactantTriethylamineHCID 8471—
ReactantHCID 15682117HCID 15682117—
SolventEthanolHCID 702—
ProductHCID 15051904HCID 15051904—

Reaction Steps

To 1.5 g of 6-chloro-9-(2'-O-methyl-β-D-ribofuranosyl)-9H-purine and 510 mg of cyclopentylamine, 1.5 ml of triethylamine and 70 ml of ethanol were added. The solution was refluxed with heating for several ten minutes to 8 hours. After washing the residue with water, methanol was added and the solution was concentrated to dryness again. The residue was recrystallized with ethyl acetate to give N6 -cyclopentyl-2'-O-methyladenosine (Compound 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04985409
Source datasetuspto-grants-1991_01
ORD IDord-0fad2de14e9b4da19001d0fbcc33a0d7
Source noteuspto-grants-1991_01