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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376651Generated: November 2, 2026

2,4-Dichloropyrimidine → Tert-butyl 4-(2-chloropyrimidin-4-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2376651

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichloropyrimidineHCID 77531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
ProductTert-butyl 4-(2-chloropyrimidin-4-yl)piperazine-1-carboxylateHCID 11197306—

Reaction Steps

A mixture of 9.55 g of tert-butyl 1-piperazinecarboxylate, 7.64 g of 2,4-dichloropyrimidine and 8.6 g of NaHCO3 in 50 ml of EtOH is heated at reflux for 1 hour. It is concentrated under vacuum, the residue is taken up in water and extracted with DCM, the organic phase is dried over Na2SO4 and the solvent is evaporated under vacuum. The residue is chromatographed on silica gel, eluting with a DCM/AcOEt (90/10 to 60/40; v/v) mixture. Two compounds are separated:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468368B2
Source datasetuspto-grants-2008_12
ORD IDord-9500ad0063f54084b120d9d9ec5dc024
Source noteuspto-grants-2008_12