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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735263Generated: October 26, 2026

Triethylamine → 10,11-Dihydro-10-(4-(4-butyloxy)benzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepine

https://huagongshe.com/reaction/1735263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Butoxybenzoyl chlorideHCID 118561—
Reactant10,11-Dihydro-5H-benzo[e]pyrrolo[1,2-a][1,4]diazepineHCID 15547048—
SolventDichloromethaneHCID 6344—
SolventSodium HydroxideHCID 14798—
Product10,11-Dihydro-10-(4-(4-butyloxy)benzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepineHCID 1891754288.9%

Reaction Steps

To a solution of 92 mg of 10, 11-dihydro-5H-pyrrolo[2, 1-c][1,4]benzodiazepine in 2 ml of methylene chloride is added 100 mg of triethylamine followed by 130 mg of 4-(n-butyloxy)benzoyl chloride. The reaction mixture is stirred am room temperature for 24 hours and then treated with 4 ml of in sodium hydroxide. The mixture is extracted with 10 ml of ethyl acetate and the extract washed with 1N sodium hydroxide and 5 ml of brine. The organic layer is dried over anhydrous sodium sulfate and filtered through hydrous magnesium silicate. The filtrate is concentrate in vacuo to a residue which is stirred with ether-hexanes to give 160 mg of the desired product as a white solid:mass spectrum (CI), 361(MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536718
Source datasetuspto-grants-1996_07
ORD IDord-db25af63e9e247d0bc3903f99528cec0
Source noteuspto-grants-1996_07