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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456263Generated: 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/1456263

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 Na2SO4 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 numberUS05843952
Source datasetuspto-grants-1998_12
ORD IDord-78b8328f251e4758b7d714ae5c69bb17
Source noteuspto-grants-1998_12