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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821307Generated: November 3, 2026

tert-Butyl piperazine-1-carboxylate → tert-Butyl 4-(5-bromopyrimidin-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1821307

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant5-Bromo-2-chloropyrimidineHCID 606665—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Producttert-Butyl 4-(5-bromopyrimidin-2-yl)piperazine-1-carboxylateHCID 2191447658%

Reaction Steps

A mixture of 5-bromo-2-chloropyrimidine (5.17 mmol) and 1,1-dimethylethyl 1-piperazinecarboxylate (11.4 mmol) in 1,4-dioxane (10 ml) was heated at reflux for 2 hours. After cooling to room temperature, the reaction mixture was diluted with water (100 ml) and ethyl acetate (100 ml). Separation of the organic layer, drying (MgSO4), filtration and concentration in vacuo provided a residue which was purified by silica gel chromatography (40 g silica gel, CHCl3/EtOAc) to give the title compound as a white solid (58%). ESMS [M+H-Boc]+: 245.0/243.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605266B2
Source datasetuspto-grants-2009_10
ORD IDord-96ada52e153849109805485d4c76e4fb
Source noteuspto-grants-2009_10