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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374285Generated: October 30, 2026

HCID 11583787, compound → HCID 11306161, compound

https://huagongshe.com/reaction/2374285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11583787HCID 11583787—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 11306161HCID 1130616194%

Reaction Steps

(2-Cyclopent-1-enyl-5-methanesulfonyl-phenyl)-[4-(4-trifluoromethyl-phenyl)-piperazin-1-yl]-methanone (Example 74) is hydrogenated in MeOH in presence of 10% Pd/C under a hydrogen pressure of 50 bar at 50° C. for 18h. Filtration, evaporation of the solvent and purification of the residue by preparative HPLC on a C-18 column with a H2O/MeCN gradient provided (2-Cyclopentyl-5-methanesulfonyl-phenyl)-[4-(4-trifluoromethyl-phenyl)-piperazin-1-yl]-methanone in 94% yield as colourless foam (M+H+: 481.5.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462617B2
Source datasetuspto-grants-2008_12
ORD IDord-dab920330243462084de8f28ad29ad79
Source noteuspto-grants-2008_12