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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1853151Generated: October 29, 2026

Diisopropylethylamine → Tert-butyl 4-(6-nitropyridin-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1853151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant5-Bromo-2-nitropyridineHCID 817620—
SolventAcetonitrileHCID 6342—
ProductTert-butyl 4-(6-nitropyridin-3-yl)piperazine-1-carboxylateHCID 1124375880%

Reaction Steps

To a stirred solution of 5-bromo-2-nitropyridine (4.93 g, 24.3 mmol) and piperazine-1-carboxylic acid tert-butyl ester (4.97 g, 26.7 mmol) in CH3CN (60 ml) is added DIPEA (4.65 mL, 26.7 mmol). The mixture is heated at reflux for 72 hours then cooled to room temperature and the precipitated product collected by filtration. The filtrate is concentrated and purified by flash column chromatography eluting with 30% EtOAc/petrol. The combined products are re-crystallized from EtOAc/petrol to give 4-(6-nitro-pyridin-3-yl)-piperazine-1-carboxylic acid tert-butyl ester, (4.50 g, 80% yield). MS (ESI) m/z 308 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962630B2
Source datasetuspto-grants-2015_02
ORD IDord-49fbf23f606d42a8add8cf4cc7728f36
Source noteuspto-grants-2015_02