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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459526Generated: November 1, 2026

Triethylamine → 4,10-Dihydro-4-(4-nitrobenzoyl)-5H-pyrrolo[1,2-a]thieno[3,2-e][1,4]diazepin

https://huagongshe.com/reaction/1459526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Nitrobenzoyl chlorideHCID 8502—
Reactant4,10-Dihydro-5H-pyrrolo[1,2-a]thieno[3,2-e][1,4]diazepineHCID 21836969—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product4,10-Dihydro-4-(4-nitrobenzoyl)-5H-pyrrolo[1,2-a]thieno[3,2-e][1,4]diazepinHCID 21837027—

Reaction Steps

To a solution of 3 mmol of 4,10-dihydro-5H-pyrrolo[1,2-a]thieno[3,2-e][1,4]diazepine in 10 ml of methylene chloride under argon is added 5 mmol of triethylamine followed by ice bath cooling. A solution of 3.3 mmol of 4-nitrobenzoyl chloride in 3 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, 2N citric acid, NaHCO3, and brine. The reaction mixture is dried with Na2SO4, filtered and evaporated in vacuo to give a solid which is purified by flash chromatography on silica gel to give desired product as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05854237
Source datasetuspto-grants-1998_12
ORD IDord-ec751a93734e4b3e8211b5220cdb5a4e
Source noteuspto-grants-1998_12