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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432138Generated: October 27, 2026

1-Ethylpiperazine → Ethyl-4-(4-nitro-pyridin-2-yl)-piperazine

https://huagongshe.com/reaction/1432138

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-EthylpiperazineHCID 79196—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloro-4-nitropyridineHCID 735152—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductEthyl-4-(4-nitro-pyridin-2-yl)-piperazineHCID 6894207068%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2 g (13 mmol) 2-chloro-4-nitropyridine, 1.73 g (15 mmol) 1-ethyl-piperazine and 0.81 g (6 mmol) N,N-diisopropylethylamine (DIPEA) in 19 ml DMF and 20 ml water was heated to 100° C. for 24 h. The precipitate was filtered off and washed three times with 4 ml of water and dried for 24 h under vacuum to yield 2.03 g (68%) of the title compound as yellow oil (m/e): 236.7 (MH+; 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612076B2
Source datasetuspto-grants-2009_11
ORD IDord-18c92dc0cb7f4bb79d58070ec4044634
Source noteuspto-grants-2009_11