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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348539Generated: October 28, 2026

HCID 86594079, compound → HCID 86594078, compound

https://huagongshe.com/reaction/348539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86594079HCID 86594079—
SolventIsopropanolHCID 3776—
ProductHCID 86594078HCID 8659407883%

Reaction Steps

The title compound, MS (ISP): m/e=490.3 (M+H+), was prepared by hydrogenation of (+/−)-4-nitro-N-phenyl-N-[cis-1-(2-phenyl-cyclohexyl)-piperidin-4-yl]-benzenesulfonamide according to the following procedure. (+/−)-4-Nitro-N-phenyl-N-[cis-1-(2-phenyl-cyclohexyl)-piperidin-4-yl]-benzenesulfonamide (0.05 g, 0.096 mmol) was suspended in isopropanol (3 ml) and the mixture was purged with argon. Palladium hydroxide on charcoal was added to the suspension, which was then put under a hydrogen atmosphere and stirred at room temperature for 20 h. The catalyst was then filtered off and the solvent was evaporated, leaving the title compound as a white foamy solid (0.039 g, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176316B2
Source datasetuspto-grants-2007_02
ORD IDord-658eedd53a5c41ec8361187b212cc944
Source noteuspto-grants-2007_02