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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439969Generated: October 25, 2026

Triethylamine → 10,11,Dihydro-10-(4-nitrobenzoyl)-5H-imidazo[2,1-c][1,4]benzodiazepine

https://huagongshe.com/reaction/439969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Nitrobenzoyl chlorideHCID 8502—
Reactant5H-Imidazo(2,1-c)(1,4)benzodiazepine, 10,11-dihydro-HCID 3060399—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product10,11,Dihydro-10-(4-nitrobenzoyl)-5H-imidazo[2,1-c][1,4]benzodiazepineHCID 21837015—

Reaction Steps

To a solution of 10 mmol of 10,11-dihydro-5H-imidazo[2,1-c][1,4]benzodiazepine in 50 ml of methylene chloride under argon is added 15 mmol of triethylamine followed by ice bath cooling. A solution of 10 mmol of 4-nitrobenzoyl chloride in 10 ml of methylene chloride is added dropwise. Following complete addition, the ice bath is removed and the reaction mixture stirred at room temperature for 2 hours. The volatiles are removed in vacuo to give a residue which is dissolved in ethyl acetate. The solution is washed with water, and brine. The organic layer is dried with Na2SO4, filtered and evaporated in vacuo to give a solid which is purified by flash chromatography to give desired product as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05516774
Source datasetuspto-grants-1996_05
ORD IDord-c5182fb4f6324f6a9c506878d0cb1ad8
Source noteuspto-grants-1996_05