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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656368Generated: October 26, 2026

Triethylamine → N-[3-[4-(2-Methoxyphenyl)-1-piperazinyl]propyl]-2-benzofurancarboxamide Dihydrochloride

https://huagongshe.com/reaction/1656368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Benzofurancarbonyl chlorideHCID 38949—
Reactant1-(3-Aminopropyl)-4-(2-methoxyphenyl)piperazineHCID 10467259—
SolventDichloromethaneHCID 6344—
ProductN-[3-[4-(2-Methoxyphenyl)-1-piperazinyl]propyl]-2-benzofurancarboxamide DihydrochlorideHCID 18995783—

Reaction Steps

To a stirred solution of [4-(2-methoxyphenyl)piperazino]propylamine (1.0 g, 0.04 mol) in 50 mL of methylene dichloride, benzofurane-2-carboxylic acid chloride (1.01 g, 0.0056 mol) and triethylamine (1 g, 0.01 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 subjected to preparative HPLC using silica gel column and ethyl acetate as the eluent. The title compound was separated and converted to the dihydrochloride salt with ethanolic HCl (0.9 g), m.p. 228°-232° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05254552
Source datasetuspto-grants-1993_10
ORD IDord-250f3df68cb24881aa589a980dc44a45
Source noteuspto-grants-1993_10