HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444961Generated: October 31, 2026
Potassium Carbonate → 3-Methyl-1-(5-nitropyridin-2-yl)piperazine
https://huagongshe.com/reaction/444961
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methylpiperazine | HCID 66057 | — |
| Reactant | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Methyl-1-(5-nitropyridin-2-yl)piperazine | HCID 44119752 | — |
Reaction Steps
872 mg (6.31 mmol) of potassium carbonate were added to a solution of 500 mg (3.15 mmol) of 2-chloro-5-nitropyridine in 7 ml of dimethylformamide. After that, a solution of 350 mg (3.32 mmol) of 2-methylpiperazine in 3 ml of dimethylformamide was slowly added dropwise to the reaction mixture while cooling with ice (exothermic reaction). The reaction mixture was stirred for 1 hour while cooling with ice and then stirred overnight at room temperature. After the solvent had been evaporated to dryness, the residue was taken up in water and this mixture was extracted three times with diethyl ether. The combined organic phases were dried over sodium sulfate, filtered and evaporated to dryness, with 3-methyl-1-(5-nitropyridin-2-yl)piperazine (Yield: 650 mg, 89% of theory) being obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476275B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-f9c6361e784f4aa9b5d2deb7274fbe83 |
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| Source note | uspto-grants-2013_07 |
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