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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610888Generated: November 3, 2026

Triethylamine → HCID 9958341, compound

https://huagongshe.com/reaction/1610888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Methylbenzoyl ChlorideHCID 13405—
ReactantHCID 18346051HCID 18346051—
SolventDichloromethaneHCID 6344—
ProductHCID 9958341HCID 995834189.2%

Reaction Steps

p-Toluoyl chloride (0.48 ml, 3.63 mmol) was added to a solution of 1(S)-[4-(3,4-dichlorobenzyl)piperazin-1-ylmethyl]-2-methylpropylamine (1 g, 3.0 mmol) and triethylamine (0.633 ml, 4.54 mmol) in methylene chloride under nitrogen atmosphere. After 1 h, the product was extracted into ethyl acetate and the organic layer was washed with sodium bicarbonate solution, dried over magnesium sulfate, filtered and concentrated in vacuo. Column chromatography with hexanes/ethyl acetate (1:2) gave N-{1(S)-[4-(3,4-dichlorobenzyl)piperazin-1-ylmethyl]-2-methylpropyl}-4-methylbenzamide (1.2 g) as an oil. The free amine was dissolved in ether and 3.5 equivalents of 1N ethereal HCl solution (10.7 ml) was added. Filtration of the resulting solid provided N-{1(S)-[4-(3,4-dichlorobenzyl)piperazin-1-ylmethyl]-2-methylpropyl}-4-methylbenzamide (1.2 g) as the bis hydrochloride salt, mp 227.8-228.9° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06984637B2
Source datasetuspto-grants-2006_01
ORD IDord-acb63dc3e3384b7dba6be7e309baeb12
Source noteuspto-grants-2006_01