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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187364Generated: October 31, 2026

Diisopropylethylamine → HCID 59830728, compound

https://huagongshe.com/reaction/1187364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Aminoadamantan-1-olHCID 2857447—
Reactant2,6-Dichlorpyridine-3-carbonyl chlorideHCID 12263984—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 59830728HCID 5983072851%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673938B2
Source datasetuspto-grants-2014_03
ORD IDord-b93b7e75d89641ea842945d496179ecf
Source noteuspto-grants-2014_03