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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367686Generated: October 30, 2026

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

https://huagongshe.com/reaction/2367686

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-nitropyridineHCID 78308—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventEthanolHCID 702—
Producttert-Butyl 4-(5-nitropyridin-2-yl)piperazine-1-carboxylateHCID 16217943127.2%

Reaction Steps

To a solution of 2-chloro-5-nitropyridine (LXV) (2.0 g, 12.6 mmol) in EtOH (20 mL) was added tert-butyl piperazine-1-carboxylate (XCVI) (7.05 g, 37.9 mmol). The reaction was headed at 70° C. for 16 h. The reaction was concentrated under vacuum and then dissolved in EtOAc. The EtOAc was washed with 1 M NaOH, brine and then dried over MgSO4 to give tert-butyl 4-(5-nitropyridin-2-yl)piperazine-1-carboxylate (XCVII) as a yellow solid (4.94 g). ESIMS found for C14H20N4O4 m/z 309.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697887B2
Source datasetuspto-grants-2014_04
ORD IDord-e4a7c68a14334127947fa70f74b08d42
Source noteuspto-grants-2014_04