HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003305Generated: October 31, 2026
Dicyclohexylcarbodiimide → N-(12-hydroxydodecyl)-6-(4-ethyl-1-piperazinyl)pyridine-3-carboxamide
https://huagongshe.com/reaction/1003305
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 12-Amino-1-dodecanol | HCID 5182020 | — |
| Reactant | Potassium 6-(4-ethyl-1-piperazinyl)pyridine-3-carboxylate | HCID 23663822 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-(12-hydroxydodecyl)-6-(4-ethyl-1-piperazinyl)pyridine-3-carboxamide | HCID 15462624 | 81.8% |
Reaction Steps
To 4.07 g of potassium 6-(4-ethyl-1-piperazinyl)-pyridine-3-carboxylate and 3.00 g of 12-aminododecanol was added 50 ml of chloroform and then 2.01 g of 1-hydroxybenzotriazole (HOBt) and 3.07 g of 1,3-dicyclohexylcarbodiimide (DCC) were added thereto while stirring at room temperature and then the mixture was stirred at room temperature for 17 hours. A further 50 ml of chloroform was added, the mixture was stirred and then insolubles were filtered off. After the residue on a filter paper was washed with chloroform, the washing and the chloroform solution were combined and washed with a 10% aqueous solution of sodium hydroxide and dried over anhydrous magnesium sulfate. After the chloroform solution was concentrated, diisopropyl ether was added and the crystal thus separated out was recovered by filtration and dried under reduced pressure to afford 5.10 g of the title compound as a crystal.
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-2cb98e0d579245e9b2224c7ee0171304 |
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| Source note | uspto-grants-2000_04 |
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