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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant12-Amino-1-dodecanolHCID 5182020—
ReactantPotassium 6-(4-ethyl-1-piperazinyl)pyridine-3-carboxylateHCID 23663822—
SolventChloroformHCID 6212—
ProductN-(12-hydroxydodecyl)-6-(4-ethyl-1-piperazinyl)pyridine-3-carboxamideHCID 1546262481.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046201
Source datasetuspto-grants-2000_04
ORD IDord-2cb98e0d579245e9b2224c7ee0171304
Source noteuspto-grants-2000_04