Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443627Generated: November 3, 2026

Triethylamine → HCID 68560231, compound

https://huagongshe.com/reaction/1443627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68559998HCID 68559998—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 68560231HCID 6856023154%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-{3-[1-(1-Benzyl-5-bromo-1H-benzimidazol-2-yl)-2-methyl-propylamino]-propyl}-isoindole-1,3-dione (260 mg, 0.56 mmol) and triethylamine (0.47 ml, 3.36 mmol) in DCM (3 ml) at 0° C., was added 4-chlorobenzoylchloride (0.36 ml, 2.8 mmol, 5 eq). The reaction mixture was stirred at 0° C. for 30 minutes. Ethyl acetate and saturated sodium bicarbonate were added. The mixture was extracted with ethyl acetate. The organic layers was combined, dried over MgSO4, filtered, and the filtrate was concentrated in vacuo. The crude material was purified by flash chromatography to give N-[1-(1-Benzyl-1H-benzimidazol-2-yl)-2-methyl-propyl]-N-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-4-chloro benzamide (182 mg, yield 54%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662581B1
Source datasetuspto-grants-2010_02
ORD IDord-2a73c903dd3e43bdbc1ccba7f0770dd4
Source noteuspto-grants-2010_02