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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820622Generated: November 1, 2026

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

https://huagongshe.com/reaction/1820622

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-nitropyridineHCID 78308—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 4-(5-nitropyridin-2-yl)piperazine-1-carboxylateHCID 16217943—

Reaction Steps

A solution of 2-chloro-5-nitropyridine (1.58 g, 10.0 mmol) in DMF (15 mL) was treated with 1-Boc-piperazine (1.96 g, 10.5 mmol) in the presence of DBU (3 mL) and Bu4NI (0.185 g, 0.5 mmol) at 80° C. for 18 h. The reaction mixture was diluted with ethyl acetate at 25° C. The organic phase was washed with H2O, saturated NaCl, dried over MgSO4 and then concentrated in vacuo to afford 4(5-nitropyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester as a yellow solid which was used for next step reaction without further purification. MS (ES+) m/z 309.4 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605161B2
Source datasetuspto-grants-2009_10
ORD IDord-2d10dcf8142247f4a82d6391ceda3cce
Source noteuspto-grants-2009_10