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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565787Generated: October 29, 2026

Triethylamine → N-cyclopropyl-6-[4-[(3-chlorophenyl)phenylmethyl]-1-piperazinyl]hexanesulfonamide

https://huagongshe.com/reaction/565787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-[(3-Chlorophenyl)phenylmethyl]piperazineHCID 4564525—
ReactantN-cyclopropyl-6-chlorohexanesulfonamideHCID 11010063—
SolventTolueneHCID 1140—
ProductN-cyclopropyl-6-[4-[(3-chlorophenyl)phenylmethyl]-1-piperazinyl]hexanesulfonamideHCID 1589570951.8%

Reaction Steps

1-[(3-Chlorophenyl)phenylmethyl]piperazine (543.7 mg, 1.90 mmol) and N-cyclopropyl-6-chlorohexanesulfonamide (500 mg, 2.09 mmol) were refluxed in toluene (15 ml) in the presence of triethylamine (211 mg, 2.09 mmol) for 48 hours. The reaction mixture was washed with water, and the organic layer was dried over anhydrous magnesium sulfate. Subsequently, the solvent was removed by evaporation in vacuo. The resulting crude product was purified by column chromatography on silica gel with chloroform-methanol (20:1), to give N-cyclopropyl-6-[4-[(3-chlorophenyl)phenylmethyl]-1-piperazinyl]hexanesulfonamide (482.7 mg) as an oil (yield based on 1-[(3-chlorophenyl)phenylmethyl]piperazine: 52.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172228B2
Source datasetuspto-grants-2001_01
ORD IDord-14110c8072074ccda7f89bcaddc1e73c
Source noteuspto-grants-2001_01