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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478633Generated: October 26, 2026

Triethylamine → N-[1-(Cyanomethyl-carbamoyl)-cyclohexyl]-4-(4-benzyl-piperazin-1-yl)-benzamide

https://huagongshe.com/reaction/478633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-Amino-cyclohexanecarboxylic acid cyanomethyl amideHCID 11194684—
Reactant4-(4-(Propan-2-yl)piperazin-1-yl)benzoic acid hydrochlorideHCID 47002203—
SolventDimethylformamideHCID 6228—
ProductN-[1-(Cyanomethyl-carbamoyl)-cyclohexyl]-4-(4-benzyl-piperazin-1-yl)-benzamideHCID 10276295—

Reaction Steps

1-Amino-cyclohexanecarboxylic acid cyanomethyl-amide (0.84 mmol), 4-[4-(2-propyl)-piperazin-1-yl]-benzoic acid hydrochloride (0.84 mmol), HOBT (0.84 mmol), WSCD (0.84 mmol) and triethylamine (0.84 mmol) are dissolved in DMF (2 ml) and stirred overnight at rt. After evaporation of the solvent, the residue is dissolved in a mixture of water and sodium carbonate (to ensure slightly basic conditions) and extracted three times with ethyl acetate. The combined extract is dried over sodium sulfate and evaporated. The residue is suspended in methanol and the solid filtered of and dried (vacuum). A pale powder with mp. 210-212° C., Rf=0.20 (CH2Cl2/MeOH=95:5) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642239B2
Source datasetuspto-grants-2003_11
ORD IDord-50853463da694ce2b86802ac58ded36b
Source noteuspto-grants-2003_11