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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43069Generated: October 29, 2026

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

https://huagongshe.com/reaction/43069

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 numberUS08536175B2
Source datasetuspto-grants-2013_09
ORD IDord-c6fcd5313b494ed990cc35f96102f438
Source noteuspto-grants-2013_09