Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288737Generated: November 1, 2026

1-Benzylpiperazine → 1-Benzyl-4-[(1-t-butoxycarbonyl-4-piperidyl)carbonyl]piperazine

https://huagongshe.com/reaction/2288737

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BenzylpiperazineHCID 75994—
ReactantSuccinimido 1-t-butoxycarbonylpiperidine-4-carboxylateHCID 15578030—
SolventDichloromethaneHCID 6344—
Product1-Benzyl-4-[(1-t-butoxycarbonyl-4-piperidyl)carbonyl]piperazineHCID 4014625—

Reaction Steps

N-Benzylpiperazine (40.0 ml) was added in one portion to a solution of succinimido 1-t-butoxycarbonylpiperidine-4-carboxylate (75.0 g) in dry dichloromethane (1600 ml). The solution was stirred at ambient temperature under an atmosphere of argon for 17 hours. The solution was washed with water (500 ml) and saturated brine (250 ml). The organic layer was dried (Na2SO4) and evaporated. The residual oil was purified by chromatography on alumina, eluting with dichloromethane to give 1-benzyl-4-[(1-t-butoxycarbonyl-4-piperidyl)carbonyl]piperazine as an oil;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090813
Source datasetuspto-grants-2000_07
ORD IDord-5aa4818ba0ba4c588412a8deb95b3af8
Source noteuspto-grants-2000_07