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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293263Generated: October 30, 2026

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

https://huagongshe.com/reaction/2293263

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 numberUS05686445
Source datasetuspto-grants-1997_11
ORD IDord-c9035b515d0649f59dca06ef991eb382
Source noteuspto-grants-1997_11