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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684526Generated: November 2, 2026

6-Aminohexanenitrile → 8-(3-(5-Cyanopentyl-amino-carbonyl)-cyclopentyl)-1,3-dipropyl-7H-purine-2,6-dione

https://huagongshe.com/reaction/1684526

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-AminohexanenitrileHCID 17079—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant8-(3-Carboxycyclopentyl)-1,3-dipropyl-7H-purine-2,6-dioneHCID 19039824—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product8-(3-(5-Cyanopentyl-amino-carbonyl)-cyclopentyl)-1,3-dipropyl-7H-purine-2,6-dioneHCID 19039838—

Reaction Steps

0.3 g (1.9 mmol) of carbonyldiimidazole are added to a suspension of 0.67 g (1.9 mmol) of 8-(3-carboxycyclopentyl)-1,3-dipropyl-7H-purine-2,6-dione in 20 ml of dichloromethane and 1 ml of tetrahydrofuran and the mixture is stirred for 35 minutes at ambient temperature. After the addition of 0.21 g (1.9 mmol) of 6-aminocapronitrile the mixture is stirred for a further 24 hours, acidified and washed with water. The organic phase is concentrated by evaporation, the residue is taken up in 5% sodium bicarbonate solution and this solution is extracted with dichloromethane. After drying and evaporation of the organic extracts the title compound is obtained in the form of crystals which, are purified with a mixture of dichloromethane/methanol in the ratio 95:5. 0.67 g (79.8% of theory) of the title compound are obtained in the form of colourless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05641784
Source datasetuspto-grants-1997_06
ORD IDord-5a3a1dbde2a94ee6b92d0d5764081195
Source noteuspto-grants-1997_06