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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337220Generated: October 30, 2026

Acryloyl chloride → 4-(4-Acryloylamino-piperidine-1-sulfonyl)-2-fluoro-N-phenethyl-benzamide

https://huagongshe.com/reaction/337220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcryloyl chlorideHCID 13140—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(4-Amino-piperidine-1-sulfonyl)-2-fluoro-N-phenethyl-benzamideHCID 71060085—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product4-(4-Acryloylamino-piperidine-1-sulfonyl)-2-fluoro-N-phenethyl-benzamideHCID 8667408725%

Reaction Steps

Diisopropylethylamine (0.51 ml, 3.0 mmol) was added in one portion to a stirred solution of 4-(4-Amino-piperidine-1-sulfonyl)-2-fluoro-N-phenethyl-benzamide (0.24 g, 0.6 mmol) in THF (10 ml), followed by the drop wise addition of acryloyl chloride (0.05 ml, 0.66 mmol) and the mixture was stirred at room temperature under a nitrogen atmosphere for 3 hours. After this time the mixture was diluted with DCM (20 ml) and washed sequentially with HCl (1M solution, 10 ml), NaOH (1M solution, 10 ml) and brine (10 ml). The organic layer was separated, dried (MgSO4), filtered, concentrated and the resulting residue was purified by flash column chromatography (elution: 98% DCM, 2% Methanol) to give the title compound (0.06 g, 25% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889716B2
Source datasetuspto-grants-2014_11
ORD IDord-0667b9706bd5435299fe90ddddf95502
Source noteuspto-grants-2014_11