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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Aminoadamantane hydrochlorideHCID 25331—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Cyclopentanecarbonyl-2,2-dimethyl-1,3-dioxane-4,6-dioneHCID 54073587—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductN-(2-adamantyl)-3-cyclopentyl-3-oxo-propanamideHCID 5951608940.7%

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816391B2
Source datasetuspto-grants-2010_10
ORD IDord-13e14de7f8d14e099e1028266ecedb38
Source noteuspto-grants-2010_10