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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656366Generated: October 29, 2026

Triethylamine → N-[2-[4-(3-Chlorophenyl)-1-piperazinyl]ethyl]tricyclo[3,3,1,13,7]decane-1-carboxamide Dihydrochloride

https://huagongshe.com/reaction/1656366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Adamantanecarbonyl chlorideHCID 98915—
Reactant2-(4-(3-Chlorophenyl)piperazin-1-yl)ethan-1-amineHCID 12726736—
SolventDichloromethaneHCID 6344—
ProductN-[2-[4-(3-Chlorophenyl)-1-piperazinyl]ethyl]tricyclo[3,3,1,13,7]decane-1-carboxamide DihydrochlorideHCID 45262376—

Reaction Steps

To a stirred solution of [4-(m-chlorophenyl)piperazino]ethylamine (2.5 g, 0.01 mol) in 50 mL of methylene chloride, adamantane-1-carboxylic acid chloride (5 g, 0.018 mol) and triethylamine (3.6 g, 0.018 mol) were added. Stirring was continued at room temperature overnight. The methylene chloride solution was washed with water, dried over anhydrous sodium sulfate and evaporated under reduced pressure. The remaining residue was dissolved in ethyl acetate (10 mL) and subjected to column chromatography using silica gel and ethyl acetate as the eluent. The title compound was separated and converted to the dihydrochloride salt with ethanolic HCl (0.7 g), m.p. 210°-213° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05254552
Source datasetuspto-grants-1993_10
ORD IDord-1a1aa8c489a54a09b16ef03b997a91ce
Source noteuspto-grants-1993_10