HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910819Generated: November 2, 2026
1-(4-Nitrophenyl)piperazine → HCID 67106340, compound
https://huagongshe.com/reaction/1910819
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(4-Nitrophenyl)piperazine | HCID 80447 | — |
| Reactant | Pyridine-3-sulfonyl chloride | HCID 3164136 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67106340 | HCID 67106340 | 39% |
Reaction Steps
To a solution of 1-(4-nitrophenyl)-piperazine (2.50 g, 12.1 mmol) in pyridine (15 mL) was added a solution of pyridine-3-sulfonyl chloride (2.78 g, 15.7 mmol) in THF (30 mL) under an argon atmosphere at 0° C. The reaction was warmed to r.t. and stirred for 2 h, before the mixture was evaporated to dryness. The residue was partitioned between water and dichloromethane, the organic layer separated and washed successively with sat. sodium bicarbonate solution, water and brine. The organics were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude residue was subjected to column chromatography over neutral alumina using 5% to 70% ethyl acetate in petroleum ether as eluent to afford 1-(4-nitrophenyl)-4-(pyridine-3-sulfonyl)-piperazine (1.63 g, 39%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08604029B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-b3cf5a73760c4cbdaaaf5e2246f9cfb4 |
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| Source note | uspto-grants-2013_12 |
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