HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189270Generated: October 29, 2026
1-Methylpiperazine → 1-Methyl-4-(6-nitropyridin-3-yl)piperazine
https://huagongshe.com/reaction/2189270
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 5-Bromo-2-nitropyridine | HCID 817620 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Methyl-4-(6-nitropyridin-3-yl)piperazine | HCID 51711484 | — |
Reaction Steps
A mixture of 5-bromo-2-nitropyridine (500 mg, 2.46 mmol) and 1-methylpiperazine (1 mL) is heated at 80° C. for 2 hour. Then water is added. The aqueous layer is extracted with EtOAc, and the organic extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The crude product is purified by column chromatography (SiO2, MeOH:CH2Cl2=0.7:99.3 to 6:93) to give 520 mg of the title compound as yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324225B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-a219be032f7241e687aa82ad7ddc8104 |
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| Source note | uspto-grants-2012_12 |
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