Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288739Generated: October 29, 2026

Ammonium formate → 1-[1-(4-Pyrimidinyl)-4-piperidylcarbonyl]piperazine

https://huagongshe.com/reaction/2288739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant1-Benzyl-4-[(1-[4-pyrimidinyl]-4-piperidyl)carbonyl]piperazineHCID 18698066—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product1-[1-(4-Pyrimidinyl)-4-piperidylcarbonyl]piperazineHCID 1869797094.3%

Reaction Steps

Ammonium formate (1.88 g) was added to a mixture of 1-benzyl-4-[(1-[4-pyrimidinyl]-4-piperidyl)carbonyl]piperazine (2.73 g) and 10% palladium on carbon catalyst (0.55 g) in methanol (70 ml) under an atmosphere of argon. The mixture was stirred at reflux temperature for 1 hour. The cooled mixture was filtered through diatomaceous earth and the filtercake was well washed with methanol. The filtrate and washings were combined and evaporated. The residual oil was suspended in saturated aqueous sodium carbonate solution (30 ml) and the mixture was extracted with dichloromethane (4×100 ml). The dichloromethane extracts were combined, dried (Na2SO4) and evaporated to give 1-[(1-[4-pyrimidinyl]-4-piperidyl)carbonyl]piperazine (1.94 g, 94%) as an off-white solid;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090813
Source datasetuspto-grants-2000_07
ORD IDord-eeb5311c887a409cb52ce77523097ce7
Source noteuspto-grants-2000_07