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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747665Generated: October 27, 2026

N-Methylethylamine → N-[2-(3-cyanophenoxy)ethyl]-4-(N-methyl-N-ethylcarbamoyl)benzamide

https://huagongshe.com/reaction/747665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylethylamineHCID 12219—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-[N-[2-(3-cyanophenoxy)ethyl]carbamoyl]benzoic acidHCID 68831518—
SolventHydrochloric AcidHCID 313—
ProductN-[2-(3-cyanophenoxy)ethyl]-4-(N-methyl-N-ethylcarbamoyl)benzamideHCID 68830104—

Reaction Steps

258 mg (0.83 mmol) of 4-[N-[2-(3-cyanophenoxy)ethyl]carbamoyl]benzoic acid, 53 mg (0.9 mmol) of N-ethyl-N-methylamine, 129 mg (0.83 mmol) of 1-hydroxybenzotriazole (hydrous, 87%) and 159 mg (0.83 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride were stirred in 10 ml of dichloro ee at room temperature overnight. The resultant mixture was diluted with 1 N hydrochloric acid. After the extraction with dichloromethane, the organic layer was washed with 1 N aqueous sodium hydroxide solution and then with saturated aqueous NaCl solution and dried over anhydrous magnesium-sulfate. The solvent was evaporated to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07396844B1
Source datasetuspto-grants-2008_07
ORD IDord-e3b794dff0b24d9bb6be2ed2c9b71621
Source noteuspto-grants-2008_07