Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517422Generated: October 30, 2026

(4-Methylpiperazin-1-yl)(4-nitrophenyl)methanone → (4-Aminophenyl)(4-methylpiperazin-1-yl)methanone

https://huagongshe.com/reaction/517422

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Methylpiperazin-1-yl)(4-nitrophenyl)methanoneHCID 716396—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(4-Aminophenyl)(4-methylpiperazin-1-yl)methanoneHCID 23140889.2%

Reaction Steps

To a solution of (4-Methyl-piperazin-1-yl)-(4-nitro-phenyl)-methanone (14 g, 0.05623 mol) in MeOH (100 mL) was added Pd/C 10% (1.4 g) in portions and the Parr reaction vessel was purged with nitrogen for 10 min. reaction vessel was fixed in Parr shaker at 60 psi pressure for 3 h. The reaction mixture was filtered through the Celite® pad and the filtrate was concentrated under reduced pressure to afford the title compound [11 g, 89%]; LC-MS (ESI): Calculated mass 219.1; Observed mass: 220.1 [M+H]+ (RT: 0.16 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115092B2
Source datasetuspto-grants-2015_08
ORD IDord-afbc65f573fb4bd087bcbe703a5efcea
Source noteuspto-grants-2015_08