Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841927Generated: November 2, 2026

Benzoyl chloride → N-[4-(4-Benzoyl-piperazine-1-sulfonyl)-phenyl]-acrylamide

https://huagongshe.com/reaction/1841927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-[4-(piperazine-1-sulfonyl)-phenyl]-acrylamideHCID 56953730—
SolventTetrahydrofuranHCID 8028—
ProductN-[4-(4-Benzoyl-piperazine-1-sulfonyl)-phenyl]-acrylamideHCID 6719476013.3%

Reaction Steps

Diisopropylethylamine (0.24 ml, 1.36 mmol) was added in one portion to a stirred solution of N-[4-(piperazine-1-sulfonyl)-phenyl]-acrylamide (0.1 g, 0.34 mmol) in THF (5 ml). The mixture was stirred at room temperature for 5 minutes before benzoyl chloride (0.05 ml, 0.44 mmol) was added drop wise and the resulting mixture was stirred at room temperature under a nitrogen atmosphere for 18 hours. The crude reaction mixture was concentrated under vacuum and the residue was purified by Prep HPLC to give the title compound (0.018 g, 13% yield) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946197B2
Source datasetuspto-grants-2015_02
ORD IDord-49ca5b650af8410d9a43bb4f4eabda26
Source noteuspto-grants-2015_02