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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478630Generated: October 26, 2026

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

https://huagongshe.com/reaction/478630

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-isopropyl-piperazin-1-yl)-benzamideHCID 10295120—

Reaction Steps

1-Amino-cyclohexanecarboxylic acid cyanomethyl-amide (0.6 mmol), 4-(4-isopropyl-piperazin-1-yl)-benzoic acid hydrochloride (0.6 mmol), HOBT (0.6 mmol), WSCD (0.6 mmol) and triethylamine (0.6 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 ethyl acetate/diethylether and the solid filtered of and dried (vacuum). A white powder with mp. 218-220° C., Rf=0.28 (CH2Cl2/MeOH=9:1) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642239B2
Source datasetuspto-grants-2003_11
ORD IDord-47e5618c6be14b3ba8ff0f38833ac7a6
Source noteuspto-grants-2003_11