Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459365Generated: October 31, 2026

Triethylamine → N-[4-[(6,11-Dihydro-5H-dibenz[b,e]azepin-5-yl)-carbonyl]phenyl]-2,3,5-trichlorobenzamide

https://huagongshe.com/reaction/1459365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,3,5-Trichlorobenzoyl chlorideHCID 13011116—
Reactant5-(4-Aminobenzoyl)-6,11-dihydro-5H-dibenz[b,e]azepineHCID 15410467—
SolventDichloromethaneHCID 6344—
ProductN-[4-[(6,11-Dihydro-5H-dibenz[b,e]azepin-5-yl)-carbonyl]phenyl]-2,3,5-trichlorobenzamideHCID 6762415799.8%

Reaction Steps

A mixture of 366 mg of 2,3,5-trichlorobenzoyl chloride and 151 mg of triethylamine in 2 ml of methylene chloride is stirred while 314 mg of 5-(4-aminobenzoyl)-6,11-dihydro-5H-dibenz[b,e]azepine in 5 ml of methylene chloride is added. Stirring is continued for 1.5 hours. The reaction mixture is partitioned with water and the organic layer is washed with 1N HCl, water, 0.5N NaOH and brine. The organic layer is dried with Na2 SO4 and passed through a pad of hydrous magnesium silicate. Hexane is added to the filtrate at the boil to give 0.52 g of white solid residue which is purified by column chromatography on silica gel by elution with 2:1 hexane-ethyl acetate to give 120 mg of the desired product as a crystalline solid, m.p. 225°-230° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05854236
Source datasetuspto-grants-1998_12
ORD IDord-d09349caacb54b63b95c33c3d6f039a5
Source noteuspto-grants-1998_12