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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443635Generated: October 31, 2026

Triethylamine → HCID 68561988, compound

https://huagongshe.com/reaction/1443635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Methylbenzoyl ChlorideHCID 13405—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68559998HCID 68559998—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 68561988HCID 6856198865.1%

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 (310 mg, 0.56 mmol) and triethylamine (0.47 ml, 3.36 mmol, 6 eq) in DCM (3 ml) at 0° C., was added p-toluoyl chloride (0.38 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-5-bromo-1H-benzimidazol-2-yl)-2-methyl-propyl]-N-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-4-methyl-benzamide (242 mg, yield 65%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662581B1
Source datasetuspto-grants-2010_02
ORD IDord-e9824af1256d4b4e90c7eccbb7a491f8
Source noteuspto-grants-2010_02