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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326571Generated: October 29, 2026

Dicyclohexylcarbodiimide → 8-Cyclopentyl-3-propyl-3,7-dihydro-purine-2,6-dione

https://huagongshe.com/reaction/326571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantCyclopentanecarboxylic acidHCID 18840—
Reactant5,6-Diamino-1-propyl-1,2,3,4-tetrahydropyrimidine-2,4-dioneHCID 10631341—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
Product8-Cyclopentyl-3-propyl-3,7-dihydro-purine-2,6-dioneHCID 15667090—

Reaction Steps

To a suspension of 5,6-diamino-1-propyl-2,4(1H, 3H)pyrimidinedione (Japanese Published Unexamined Patent Application No. 57517/80) in 600 ml of dimethylformamide were sequentially added 17.7 ml (163 mmol) of cyclopentanecarboxylic acid, 30.0 g (196 mmol) of hydroxybenzotriazole and 50.5 g (245 mmol) of dicyclohexylcarbodiimide. The mixture was stirred at room temperature overnight. Insoluble materials were filtered off and the solvent was evaporated under reduced pressure After 600 ml of 4N aqueous sodium hydroxide solution was added to the residue, the mixture was refluxed for 10 minutes under heating. Under ice cooling, insoluble materials were filtered off and 50 ml of methanol was added to the filtrate. After neutralization with conc. hydrochloric acid, the precipitate was collected by filtration to afford 28.3 g (yield, 66%) of Compound c.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05270316
Source datasetuspto-grants-1993_12
ORD IDord-f57ed1ab24b842a098d0dcd895749ed8
Source noteuspto-grants-1993_12