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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2391782Generated: October 30, 2026

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

https://huagongshe.com/reaction/2391782

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IsopropylpiperazineHCID 78013—
Reactant2-Chloro-5-nitropyridineHCID 78308—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-Isopropyl-4-(5-nitro-pyridin-2-yl)-piperazineHCID 33995718—

Reaction Steps

1-Isopropylpiperazine (1.8 mL, 12.7 mmol, 2 equiv) was added to a cold (5° C.) solution of 2-chloro-5-nitropyridine (1 g, 6.3 mmol,) in DCM (5 mL). The reaction mixture was allowed to warm to rt, stirred for 16 h, diluted with DCM and H2O. The aqueous layer was separated and extracted with DCM. The organic phase was washed with brine, dried (Na2SO4), filtered and concentrated to provide 1.58 g of he title compound as a yellow solid: ESI-MS: 251.2 [M+H]+; tR=2.20 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273882B2
Source datasetuspto-grants-2012_09
ORD IDord-7b8ff1ebddd94ac5825eda769ab314c3
Source noteuspto-grants-2012_09