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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563143Generated: October 30, 2026

Piperidine → HCID 67005741, compound

https://huagongshe.com/reaction/563143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 67005749HCID 67005749—
SolventDimethylformamideHCID 6228—
ProductHCID 67005741HCID 6700574182.5%

Reaction Steps

4-(2-{(4-pentyl-benzyl)-[3-(4-trifluoromethyl-phenyl)-acryloyl]-amino}-(S)-3-phenyl-propionyl)-piperazine-1-carboxylic acid 9H-fluoren-9-ylmethyl ester (1.75 g, 2.15 mmol) was dissolved in DMF (47.5 mL) and piperidine (2.5 mL) was added. Stirring was continued at rt for 30 min. EtOAc (150 mL) was added and the mixture was washed with water (2×150 mL). The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography (silicagel, MeOH/DCM=1/99) to give 1.05 g (82.5%) of N—((S)-1-Benzyl-2-oxo-2-piperazin-1-yl-ethyl)-N-(4-pentyl-benzyl)-3-(4-trifluoromethyl-phenyl)-acrylamide. LC-MS: tR=0.97 min; [M+H]+=592.19.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067419B2
Source datasetuspto-grants-2011_11
ORD IDord-a8891680537e47d9817ce0baa7ca7644
Source noteuspto-grants-2011_11