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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236412Generated: November 1, 2026

Triethylamine → tert-Butyl 4-(5-nitropyridin-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2236412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Bromo-5-nitropyridineHCID 78240—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventAcetonitrileHCID 6342—
Producttert-Butyl 4-(5-nitropyridin-2-yl)piperazine-1-carboxylateHCID 1621794399.6%

Reaction Steps

A mixture of 2-bromo-5-nitro-pyridine (1.719 g, 8.468 mmol), piperazine-1-carboxylic acid tert-butyl ester (1.58 g, 8.468 mmol), triethylamine (3.54 mL, 25.4 mmol) in acetonitrile (6 mL) is heated at 86 C for 2 h. After it is evaporated, the residue is dissolved in methylene chloride, and washed with saturated sodium bicarbonate solution. The organic layer is evaporated to yield 2.6 g (99%) of the title compound as a pale-yellow solid. NMR (CDCl3) showed it is pure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713994B2
Source datasetuspto-grants-2010_05
ORD IDord-3c9e12781b1c46bd9779d66e85db08fc
Source noteuspto-grants-2010_05