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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187612Generated: October 31, 2026

Triethylamine → HCID 53734757, compound

https://huagongshe.com/reaction/2187612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-(4-fluorophenyl)-2-(1H-imidazol-1-yl)ethan-1-oneHCID 5151279—
ReactantHCID 18476027HCID 18476027—
CatalystDiamminetetrachlorotitanate(IV)HCID 160960—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 53734757HCID 5373475752%

Reaction Steps

Titanium chloride (2.86 ml; 26 mmol) was added portionwise to a solution of methyl 4-amino-2-(4-fluorophenyl)benzoate (5 g; 20 mmol), 1-(4-fluorophenyl)-2-(imidazol-1-yl) ethanone (4.08 g; 20 mmol) and triethylamine (8.4 ml; 60 mmol) in dichloromethane (120 ml) at 0° C. under argon atmosphere. After stirring overnight at ambient temperature, sodium cyanoborohydride (1.4 g; 0.22 mmol) in solution in methanol (10 ml) was added at 0° C. The reaction mixture was stirred for 2 hours at ambient temperature, treated with 5% aqueous sodium hydrogen carbonate solution, filtered and extracted with dichloromethane. After evaporation to dryness of the organic phase, the residue was purified by flash chromatography eluting with dichloromethane/ethanol 95/5 to give methyl 4-[1-(4-fluorophenyl)-2-(imidazol-1-yl)ethylamino]-2-(4-fluorophenyl)benzoate. Yield 52%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410539B1
Source datasetuspto-grants-2002_06
ORD IDord-df3c8ec8df954fa1aee550a7315bab36
Source noteuspto-grants-2002_06