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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504228Generated: October 26, 2026

Potassium Carbonate → 1-Ethyl-3,3,5-trimethyl-7-[3-(2-phenyl-benzoimidazol-1-yl)propoxy]-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione hydrochloride

https://huagongshe.com/reaction/1504228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-PhenylbenzimidazoleHCID 12855—
ReactantEthanol hydrochlorideHCID 21887872—
Reactant1-Ethyl-7-(3-iodopropoxy)-3,3,5-trimethyl-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dioneHCID 68672792—
SolventIsopropanolHCID 3776—
SolventDimethylformamideHCID 6228—
Product1-Ethyl-3,3,5-trimethyl-7-[3-(2-phenyl-benzoimidazol-1-yl)propoxy]-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione hydrochlorideHCID 70656674—

Reaction Conditions

Temperature60 °C

Reaction Steps

2-Phenyl-1H-benzimidazole(0.2 g) and potassium carbonate(0.29 g) were added to a DMF solution(5 ml) of 1-ethyl-7-(3-iodopropoxy)-3,3,5-trimethyl-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione(0.49 g). The mixture was stirred at 60° C. for 7 hours. The reaction mixture was poured to ice water(50 ml), and the generated insoluble matter was separated. The insoluble matter was dissolved in ethyl acetate. The liquid was dried over sodium sulfate and condensed under reduced pressure. The residue was purified by silica gel column chromatography (hexane: ethyl acetate=1:3). The purified product was condensed under reduced pressure. A 1N-hydrogen chloride ethanol solution(1.0 ml) was added to an isopropyl alcohol solution of the residue. The mixture was condensed under reduced pressure. Ether was added to the residue. The generated insoluble matter was separated by filtration and dried to give the title compound(0.32 g) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212187B2
Source datasetuspto-grants-2015_12
ORD IDord-df9842b6d27f4b3c9c25b2649a2578b7
Source noteuspto-grants-2015_12