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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890566Generated: October 31, 2026

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

https://huagongshe.com/reaction/890566

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichloropyrimidineHCID 77531—
Reactant1-Boc-4-methylpiperazineHCID 11401394—
SolventTolueneHCID 1140—
Producttert-Butyl 4-(4-chloropyrimidin-2-yl)piperazine-1-carboxylateHCID 4673827056.9%

Reaction Steps

To a suspension of 2,4-dichloropyrimidine (1.00 g, 6.71 mmol) in 13.4 mL of toluene was added 4-methyl-piperazine-1-carboxylic acid tert-butyl ester (1.34 g, 6.71 mmol). The reaction was heated to reflux overnight, then cooled to room temperature and concentrated in vacuo. The residue was taken up in 20 mL of water and extracted with ethyl acetate (2×40 mL). The combined organic layers were washed with brine (25 mL), then dried over sodium sulfate, filtered, and concentrated in vacuo to an off-white solid. Flash column chromatography (silica gel, gradient elution from 5% ethyl acetate-hexanes to 20% ethyl acetate-hexanes) yielded 1.14 g of the title compound (I-2a).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06995159B2
Source datasetuspto-grants-2006_02
ORD IDord-ecaa0ddc47c040cf8f7aea32f78f69bb
Source noteuspto-grants-2006_02