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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456285Generated: October 26, 2026

Triethylamine → N-[4-[(Dibenz[b,f] [1,4]thiazepin-10(11H)-yl)carbonyl]phenyl]-2,4-dichlorobenzamide

https://huagongshe.com/reaction/1456285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4-Dichlorobenzoyl chlorideHCID 66645—
Reactant10,11-Dihydro-10-(4-aminobenzoyl)dibenz[b,f][1,4]thiazepineHCID 54230002—
SolventDichloromethaneHCID 6344—
ProductN-[4-[(Dibenz[b,f] [1,4]thiazepin-10(11H)-yl)carbonyl]phenyl]-2,4-dichlorobenzamideHCID 6762559678.9%

Reaction Steps

To a solution of 452 mg of 2,4-dichlorobenzoyl chloride in 6 ml of methylene chloride is added 0.6 g of 10-(4-aminobenzoyl)-10,11-dihydrodibenz[b,f][1,4]thiazepine followed by 0.375 ml of triethylamine. The reaction mixture is stirred at room temperature for 18 hours. The reaction mixture is washed with 20 ml of water, 1N HCl, 1N Na2CO3, water and dried over MgSO4. The filtrate is evaporated in vacuo to give 0.72 g of yellowish solid which is purified by silica gel chromatography on thick layer plates by elution with 1:1 ethyl acetate-hexane to give 0.254 g of the desired product as ivory crystals, m.p. 112°-115° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843952
Source datasetuspto-grants-1998_12
ORD IDord-5de60e319f454eb3a97e44d50e28b0bb
Source noteuspto-grants-1998_12