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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409696Generated: October 29, 2026

1-Isopropylpiperazine → 1-Isopropyl-4-(5-nitro-pyridin-2-yl)-piperazine

https://huagongshe.com/reaction/409696

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IsopropylpiperazineHCID 78013—
Reactant2-Chloro-5-nitropyridineHCID 78308—
SolventDichloromethaneHCID 6344—
SolventWater methylene chlorideHCID 21908982—
Product1-Isopropyl-4-(5-nitro-pyridin-2-yl)-piperazineHCID 33995718—

Reaction Steps

N-Isopropylpiperazine (1.8 mL, 12.7 mmol, 2 equiv) is added to a cold (5° C.) mixture of 2-chloro-5-nitropyridine (1 g, 6.3 mmol) in DCM (5 mL). The reaction mixture is allowed to warm to RT, stirred for 16 h, diluted with DCM/H2O and extracted with DCM. The organic phase is washed with brine, dried (Na2SO4), filtered and concentrated to provide the title compound as a yellow solid: ES-MS: 251.2 [MH]+; tR=2.20 min (system 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759517B2
Source datasetuspto-grants-2014_06
ORD IDord-dd6b601e431044f79c224e3d95dd12c4
Source noteuspto-grants-2014_06