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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639159Generated: November 1, 2026

Triethylamine → HCID 10572963, compound

https://huagongshe.com/reaction/1639159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDiphosgeneHCID 10426—
ReactantAmantadine HydrochlorideHCID 64150—
Reactant3-(4-Pyrimidin-2-ylpiperazin-1-yl)propan-1-amineHCID 10704227—
SolventDichloromethaneHCID 6344—
ProductHCID 10572963HCID 10572963—

Reaction Steps

To a stirred suspension of 1-adamantanamine hydrochloride (1.25 gm, 0.0067 mol) and triethylamine (2.7 gm, 0.027 mol) in 25 mol of dry methylene chloride under a dry nitrogen atmosphere was added, dropwise, trichloromethyl chloroformate (1.33 gm, 0.0033 mol). The resulting suspension was refluxed for three hours, and then a solution of 3-[4-(2-pyrimidyl)-1-piperazinyl]propylamine (1.44 gm, 0.0067 mol) in 15 ml of dry methylene chloride was added. The resulting mixture was allowed to stir at room temperature overnight. The reaction mixture was then diluted to 200 ml with methylene chloride, washed with 3% aqueous sodium bicarbonate solution, dried over anhydrous sodium sulfate, and concentrated on a rotary evaporator. The title compound (TLC on silica gel using a 30% methanol in ethyl acetate solvent system, Rf=0.39) was isolated by gravity chromatography on silica gel and recrystallized from methylene chloride/hexane (1.76 gm, 60% of theory), mp.=172°-173° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04882432
Source datasetuspto-grants-1989_11
ORD IDord-698f22d69bd24b88bcfc30a792b4b27a
Source noteuspto-grants-1989_11