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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534929Generated: October 31, 2026

Triethylamine → HCID 66750881, compound

https://huagongshe.com/reaction/534929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantMonoethyl malonateHCID 70615—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantSodium BicarbonateHCID 516892—
ReactantPiperazine, 1-[4-bromo-2-(1,1-dimethylethyl)phenyl]-, hydrochloride (1:2)HCID 66751142—
SolventAcetonitrileHCID 6342—
ProductHCID 66750881HCID 6675088193%

Reaction Steps

A suspension of 1-(4-bromo-2-tert-butylphenyl)piperazine dihydrochloride (Reference Example 9, 0.300 g, 0.81 mmol), 3-ethoxy-3-oxopropanoic acid (0.128 g, 0.97 mmol), EDCI (0.186 g, 0.972 mmol), HOBt (0.131 g, 0.972 mmol) and triethylamine (339 4.05 mmol) in acetonitrile (10 mL) was stirred at room temperature for 16 h. The reaction mixture was poured into saturated sodium hydrogen carbonate solution and extracted with ethyl acetate. The organic layer was washed with saturated sodium hydrogen carbonate solution and brine, dried over MgSO4, and the solvent was evaporated under reduced pressure to give the crude product. The product was purified by flash column chromatography (silica gel, n-hexane/ethyl acetate=80:20 to 50:50) to provide ethyl 3-[4-(4-bromo-2-tert-butylphenyl)piperazin-1-yl]-3-oxopropanoate (0.308 g, 93%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-ac8546e8df9a409f8b772fd3c2835cd8
Source noteuspto-grants-2014_10