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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Aminohexanenitrile | HCID 17079 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 8-(3-Carboxycyclopentyl)-1,3-dipropyl-7H-purine-2,6-dione | HCID 19039824 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-(3-(5-Cyanopentyl-amino-carbonyl)-cyclopentyl)-1,3-dipropyl-7H-purine-2,6-dione | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05641784 |
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| Source dataset | uspto-grants-1997_06 |
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| ORD ID | ord-5a3a1dbde2a94ee6b92d0d5764081195 |
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| Source note | uspto-grants-1997_06 |
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