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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038518Generated: November 2, 2026

3-[2-(4-{5-[1,1,1,3,3,3-Hexafluoro-2-(4-methoxybenzyloxy)propan-2-yl]-4-propylpyridin-2-yl}piperazin-1-yl)ethyl]-5-[4-(1-methylethoxy)phenyl]-5-methylimidazolidine-2,4-dione → 3-(2-{4-[5-(1,1,1,3,3,3-Hexafluoro-2-hydroxypropan-2-yl)-4-propylpyridin-2-yl]piperazin-1-yl}ethyl)-5-[4-(1-methylethoxy)phenyl]-5-methylimidazolidine-2,4-dione

https://huagongshe.com/reaction/1038518

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[2-(4-{5-[1,1,1,3,3,3-Hexafluoro-2-(4-methoxybenzyloxy)propan-2-yl]-4-propylpyridin-2-yl}piperazin-1-yl)ethyl]-5-[4-(1-methylethoxy)phenyl]-5-methylimidazolidine-2,4-dioneHCID 86647181—
CatalystHCID 178418390HCID 178418390—
SolventEthyl AcetateHCID 8857—
Product3-(2-{4-[5-(1,1,1,3,3,3-Hexafluoro-2-hydroxypropan-2-yl)-4-propylpyridin-2-yl]piperazin-1-yl}ethyl)-5-[4-(1-methylethoxy)phenyl]-5-methylimidazolidine-2,4-dioneHCID 5956391286.3%

Reaction Steps

3-[2-(4-{5-[1,1,1,3,3,3-Hexafluoro-2-(4-methoxybenzyloxy)propan-2-yl]-4-propylpyridin-2-yl}piperazin-1-yl)ethyl]-5-[4-(1-methylethoxy)phenyl]-5-methylimidazolidine-2,4-dione (10 mg, 0.0131 mmol) was dissolved in ethyl acetate (2 mL), added palladium carbon (1.0 mg), and the mixture was stirred at room temperature for 6 hours under a hydrogen atmosphere. The reaction solution was filtered through a pad of celite, and concentrated in vacuo. The title compound (7.3 mg (yield 86%)) was obtained as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551985B2
Source datasetuspto-grants-2013_10
ORD IDord-717a7faf55514353b74499b0e07c2a9b
Source noteuspto-grants-2013_10