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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409629Generated: October 31, 2026

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

https://huagongshe.com/reaction/2409629

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 33995718100.2%

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 the 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 numberUS08815901B2
Source datasetuspto-grants-2014_08
ORD IDord-1080da4e757142cc84808d918464dbcd
Source noteuspto-grants-2014_08