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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189754Generated: October 30, 2026

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

https://huagongshe.com/reaction/1189754

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 numberUS08674099B2
Source datasetuspto-grants-2014_03
ORD IDord-a58b1de41652438c962c7a6aa2ba209d
Source noteuspto-grants-2014_03