HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485489Generated: October 30, 2026
2-Chloro-5-nitropyridine → 1-Ethyl-4-(5-nitropyridin-2-yl)piperazine
https://huagongshe.com/reaction/1485489
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| Reactant | 1-Ethylpiperazine | HCID 79196 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-Ethyl-4-(5-nitropyridin-2-yl)piperazine | HCID 2848980 | 88% |
Reaction Steps
2-Chloro-5-nitropyridine (800 mg, 5.05 mmol) was dissolved in dioxane (20 mL) and then 1-ethylpiperazine (1.7 g, 15.15 mmol) and N,N-diisopropylethylamine (927 mL, 5.05 mmol) were added. The reaction mixture solution was stirred at 70° C. for a day. The reaction solution was cooled to room temperature, diluted with ethyl acetate, and then washed with brine. The organic layer was concentrated by drying with magnesium sulfate. The target compound (1.05 g, 87% yield) was used in the following reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422307B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-9d618501bbbb48b1ac2129bfe2c05047 |
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| Source note | uspto-grants-2016_08 |
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