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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29001Generated: October 30, 2026

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

https://huagongshe.com/reaction/29001

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 numberUS07419988B2
Source datasetuspto-grants-2008_09
ORD IDord-7e3f5a82c4654e8ca0222ca8d720a2d1
Source noteuspto-grants-2008_09