HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160550Generated: November 1, 2026
2-Aminoadamantane hydrochloride → N-(2-adamantyl)-3-cyclopentyl-3-oxo-propanamide
https://huagongshe.com/reaction/1160550
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Aminoadamantane hydrochloride | HCID 25331 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Cyclopentanecarbonyl-2,2-dimethyl-1,3-dioxane-4,6-dione | HCID 54073587 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(2-adamantyl)-3-cyclopentyl-3-oxo-propanamide | HCID 59516089 | 40.7% |
Reaction Steps
2-Adamantanamine hydrochloride (1.641 g, 8.74 mmol) was added to 5-(cyclopentanecarbonyl)-2,2-dimethyl-1,3-dioxane-4,6-dione (Intermediate#77), (2.1 g, 8.74 mmol) and N-Ethyldiisopropylamine (1.512 mL, 8.74 mmol) in toluene (30 mL). The resulting suspension was stirred at 110° C. for 2 hours. The reaction mixture was diluted with EtOAc (100 mL), and washed sequentially with 2M HCl (20 mL), and water (2×50 mL). The organic layer was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 100% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford N-(2-adamantyl)-3-cyclopentyl-3-oxo-propanamide (1.030 g, 40.7%) as a brown oil which crystallised on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07816391B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-13e14de7f8d14e099e1028266ecedb38 |
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| Source note | uspto-grants-2010_10 |
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