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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465467Generated: November 1, 2026

Triethylamine → tert-Butyl 4-(4-chloropyrimidin-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1465467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4,6-DichloropyrimidineHCID 70943—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventIsopropanolHCID 3776—
Producttert-Butyl 4-(4-chloropyrimidin-2-yl)piperazine-1-carboxylateHCID 4673827095%

Reaction Steps

To a solution (60 ml) of 4,6-dichloropyrimidine (2.00 g, 13.4 mmol) and tert-butyl piperazine-1-carboxylate (3.00 g, 16.1 mmol) in 2-propanol was added triethylamine (4.7 ml, 33.6 mmol), and the mixture was heated under reflux for 2 hrs. The mixture was concentrated under reduced pressure, dichloromethane was added to the residue, and the mixture was washed with water. The aqueous layer was extracted with dichloromethane, and the combined organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:2) to give tert-butyl 4-(6-chloropyrimidin-2-yl)piperazine-1-carboxylate (3.80 g, yield 95%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999989B2
Source datasetuspto-grants-2015_04
ORD IDord-1d842dd940ed4b08a93ae1f39cf56f70
Source noteuspto-grants-2015_04