HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2424914Generated: November 1, 2026
Amantadine → N-adamantan-1-yl-2,6-dichloronicotinamide
https://huagongshe.com/reaction/2424914
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Amantadine | HCID 2130 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,6-Dichlorpyridine-3-carbonyl chloride | HCID 12263984 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-adamantan-1-yl-2,6-dichloronicotinamide | HCID 59830746 | 85.6% |
Reaction Steps
A solution of 2,6-dichloronicotinoyl chloride (4.21 g, 20 mmol) in DCM (20 mL) was added dropwise to a stirred suspension of 1-aminoadamantane (3.03 g, 20 mmol) and N-ethyldiisopropylamine (4.19 mL, 24 mmol) in DCM (20 mL) at 0° C., over a period of 30 minutes under nitrogen. The resulting suspension was stirred at room temperature for 18 hours. The reaction mixture was diluted with EtOAc (500 mL), and washed sequentially with water (100 mL) and saturated brine (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 5% Et2O in DCM. Pure fractions were evaporated to dryness to afford N-adamantan-1-yl-2,6-dichloronicotinamide (5.57 g, 76%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07964618B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-309d137102ab4bd0956b6aab7fb0a4e7 |
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| Source note | uspto-grants-2011_06 |
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