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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727833Generated: November 2, 2026

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

https://huagongshe.com/reaction/1727833

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 numberUS07495102B2
Source datasetuspto-grants-2009_02
ORD IDord-bb4211f360c940f58445e055ef81c6c9
Source noteuspto-grants-2009_02