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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1938322Generated: October 26, 2026

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

https://huagongshe.com/reaction/1938322

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 numberUS05693635
Source datasetuspto-grants-1997_12
ORD IDord-fdc632cde6ae46f395fe2eae55b43c2e
Source noteuspto-grants-1997_12