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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18406Generated: October 30, 2026

2-(Adamantan-1-yl)-N-methylethan-1-amine → HCID 21974209, compound

https://huagongshe.com/reaction/18406

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Adamantan-1-yl)-N-methylethan-1-amineHCID 35996—
ReactantDiisopropylethylamineHCID 81531—
ReactantTriphosgeneHCID 94429—
ReactantN-Methyl-3-(pyridin-4-yl)propan-1-amineHCID 21974070—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 21974209HCID 21974209141.6%

Reaction Steps

A solution of triphosgene (190 mg, 0.640 mmol) in dichloromethane (6.0 ml) was stirred at room temperature under a nitrogen atmosphere. A solution of 2-(1-adamantyl)-N-methylethylamine (Intermediate No. 3-1, 330 mg, 1.71 mmol) and diisopropylethylamine (0.357 ml, 2.05 mmol) in dichloromethane (6.0 ml) was added dropwise thereto over 17 minutes. After eight minutes, a solution of N-methyl-3-(4-pyridyl)propylamine (Intermediate No. 3-3, 264 mg, 1.78 mmol) and diisopropylethylamine (0.357 ml, 2.05 mmol) in dichloromethane (5.1 ml) was added to the mixture all at once, and the whole was stirred for 20 hours. The reaction mixture was diluted with diethyl ether (40 ml), the whole was washed with a saturated aqueous sodium hydrogencarbonate solution (40 ml) twice and a saturated aqueous sodium chloride solution (40 ml) successively, and the organic layer was dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography to give the target compound (335 mg, 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741346B2
Source datasetuspto-grants-2010_06
ORD IDord-cd3da273f43049dbbedd26fabce8ed1e
Source noteuspto-grants-2010_06