Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232395Generated: October 25, 2026

Piperazine,1-(4-nitrophenyl)-4-(4-pyridinyl)- → 1-(4-Aminophenyl)-4-(4-pyridyl)piperazine

https://huagongshe.com/reaction/2232395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazine,1-(4-nitrophenyl)-4-(4-pyridinyl)-HCID 10924082—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-(4-Aminophenyl)-4-(4-pyridyl)piperazineHCID 1089046158.3%

Reaction Steps

A mixture of 1-(4-nitrophenyl)-4-(4-pyridyl)piperazine (2.07 g) in ethanol (100 ml) was hydrogenated at room temperature under a pressure of 2 bars in the presence of 10% palladium on charcoal (0.25 g). When reduction was complete, the catalyst was filtered off and the filtrate was evaporated. The residue was crystallised from methanol/ethyl acetate to give 1-(4-aminophenyl)-4-(4-pyridyl)piperazine (1.08 g), m.p. 210°-211° C. Found: C,70.47; H,7.07; N,21.56. C15H18N4 requires: C,70.83; H,7.13; N,22.03%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04788196
Source datasetuspto-grants-1988_11
ORD IDord-724f0bbbf4eb4edaa1696d9bcefb874d
Source noteuspto-grants-1988_11