Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436762Generated: November 1, 2026

Ethylene Glycol → Tert-butyl 4-(5-bromopyridin-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1436762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant3-Bromo-5-iodopyridineHCID 820409—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventIsopropanolHCID 3776—
ProductTert-butyl 4-(5-bromopyridin-3-yl)piperazine-1-carboxylateHCID 1165304937%

Reaction Steps

A solution of 3-bromo-5-iodopyridine (13.0 g, 45.8 mmol) , tert-butyl piperazine-1-carboxylate (8.53 g, 45.8 mmol) , copper(I) iodide (0.871 g, 4.57 mmol), K3PO4 (19.46 g, 91.68 mmol), 1,2-ethanediol (5.1 mL, 91 mmol) in isopropyl alcohol (80 mL) in a sealed tube was heated at 80° C. in an oil bath for 2 days. After cooling to room temperature, the reaction mixture was filtered through celite. The filtrate was concentrated in vacuo. The residue was taken up in EtOAc and the solution was washed with saturated NaHCO3, dried (MgSO4) and concentrated. Purification by flash chromatography on silica gel (20% EtOAc/hexanes to 30% EtOAc/hexanes) afforded 5.75 g (37%) of desired product. MS calculated for C14H20BrN3O2: (M+H) 343; found 342.0, 344.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618970B2
Source datasetuspto-grants-2009_11
ORD IDord-e20fbbdc30b2460389eaed0e6c9525c6
Source noteuspto-grants-2009_11