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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565770Generated: October 29, 2026

1-(Bis(4-fluorophenyl)methyl)piperazine → N-(2-hydroxyethyl)-5-[4-[bis(4-fluorophenyl)methyl]-1-piperaziny]pentanesulfonamide

https://huagongshe.com/reaction/565770

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Bis(4-fluorophenyl)methyl)piperazineHCID 152932—
ReactantN-(2-hydroxyethyl)-5-chloropentanesulfonamideHCID 22111547—
SolventDiisopropylethylamineHCID 81531—
ProductN-(2-hydroxyethyl)-5-[4-[bis(4-fluorophenyl)methyl]-1-piperaziny]pentanesulfonamideHCID 6998935794%

Reaction Steps

1-[Bis(4-fluorophenyl)methyl]piperazine (576.7 mg, 2.00 mmol) and N-(2-hydroxyethyl)-5-chloropentanesulfonamide (459.5 mg, 2.00 mmol) were refluxed in N-ethyldiisopropylamine (2 ml) for 6 hours. The reaction mixture was concentrated in vacuo, and water was added thereto. The mixture was extracted with chloroform. The chloroform layer was washed with water, and 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-(2-hydroxyethyl)-5-[4-[bis(4-fluorophenyl)methyl]-1- piperaziny]pentanesulfonamide (905.6 mg) as a pale yellow oil (94.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172228B2
Source datasetuspto-grants-2001_01
ORD IDord-49edbcf0f1eb4239b3082b55fae12867
Source noteuspto-grants-2001_01