HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003292Generated: November 1, 2026
Potassium Iodide → N-(12-Iodododecyl)-6-(4-ethyl-1-piperazinyl)pyridine-3-carboxamide
https://huagongshe.com/reaction/1003292
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-(12-hydroxydodecyl)-6-(4-ethyl-1-piperazinyl)pyridine-3-carboxamide | HCID 15462624 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Phosphoric Acid | HCID 1004 | — |
| Product | N-(12-Iodododecyl)-6-(4-ethyl-1-piperazinyl)pyridine-3-carboxamide | HCID 15462630 | 87.1% |
Reaction Steps
To a solution of 0.26 g of potassium iodide in 2 ml of phosphoric acid was added 0.10 g of N-(12-hydroxydodecyl)-6-(4-ethyl-1-piperazinyl)pyridine-3-carboxamide and the mixture was stirred at 110° C. for 3 hours. The reaction solution was diluted with water, and a saturated aqueous solution of sodium hydrogen carbonate and an aqueous solution of sodium thiosulfate were added. The mixture was extracted with chloroform. The organic layer was washed with water and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to afford 0.11 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06046201 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-629c89687fa34263a460598c63503f4a |
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| Source note | uspto-grants-2000_04 |
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