Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289552Generated: October 29, 2026

Triethylamine → tert-Butyl 4-(6-chloropyrimidin-4-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2289552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4,6-DichloropyrimidineHCID 70943—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventEthanolHCID 702—
Producttert-Butyl 4-(6-chloropyrimidin-4-yl)piperazine-1-carboxylateHCID 1869798087.7%

Reaction Steps

A solution of 4,6-dichloropyrimidine (10.05 g), tert-butoxycarbonylpiperazine (11.94 g) and triethylamine (28.20 ml) in ethanol (150 ml) was heated at reflux for 18 hours. Solvent was evaporated and the residue dissolved in ethyl acetate and washed with water, saturated aqueous ammonium chloride solution, dried (Na2SO4) and evaporated. Recrystallisation from ethyl acetate/hexane gave, as a solid 1-(tert-butoxycarbonyl)-4-(6-chloro-pyrimidin-4-yl)piperazine (16.80 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093718
Source datasetuspto-grants-2000_07
ORD IDord-414cbabc022149c8a414726351015ddb
Source noteuspto-grants-2000_07