HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187364Generated: October 31, 2026
Diisopropylethylamine → HCID 59830728, compound
https://huagongshe.com/reaction/1187364
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Aminoadamantan-1-ol | HCID 2857447 | — |
| Reactant | 2,6-Dichlorpyridine-3-carbonyl chloride | HCID 12263984 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59830728 | HCID 59830728 | 51% |
Reaction Steps
A solution of 2,6-dichloronicotinoyl chloride (25.2 g, 119.60 mmol) in DCM (100 mL) was added dropwise to a stirred suspension of 4-aminoadamantan-1-ol (20.00 g, 119.6 mmol) and N-Ethyldiisopropylamine (24.83 mL, 143.52 mmol) in THF (400 mL) at 20° 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 the crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 100% EtOAc in DCM. Pure fractions were evaporated to dryness to afford 2,6-dichloro-N-(5-hydroxyadamantan-2-yl)nicotinamide (20.65 g, 51%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08673938B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-b93b7e75d89641ea842945d496179ecf |
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| Source note | uspto-grants-2014_03 |
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