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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478646Generated: October 29, 2026

Triethylamine → HCID 10202732, compound

https://huagongshe.com/reaction/478646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-Amino-cyclohexanecarboxylic acid cyanomethyl amideHCID 11194684—
Reactant4-[1-(2-Methoxy-ethyl)-piperidin-4-yl]-benzoic acid hydrochlorideHCID 69130206—
SolventDimethylformamideHCID 6228—
ProductHCID 10202732HCID 10202732—

Reaction Steps

1-Amino-cyclohexanecarboxylic acid cyanomethyl-amide (107 mmol), 4-[1-(2-methoxy-ethyl)-piperidin-4-yl]-benzoic acid hydrochloride (107 mmol), HOBT (107 mmol), WSCD (107 mmol) and triethylamine (107 mmol) are dissolved in DMF (250 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 purified by flash chromatography on silica gel with CH2Cl2/MeOH (with 2N NH3)=9:1 as mobile phase. The product containing fractions are combined and evaporated. The residue is suspended in diethylether/ethyl acetate and the solid filtered of and dried (vacuum). A pale powder with mp. 160-162° C., Rf=0.42 (CH2Cl2/MeOH (with 3N NH3)=9:1) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642239B2
Source datasetuspto-grants-2003_11
ORD IDord-a5c59f9bb9b24013beda367b3cece5cd
Source noteuspto-grants-2003_11