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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374843Generated: October 30, 2026

Triethylamine → HCID 59853884, compound

https://huagongshe.com/reaction/2374843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPivaloyl chlorideHCID 62493—
ReactantSodium BicarbonateHCID 516892—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
ReactantHCID 59853907HCID 59853907—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 59853884HCID 59853884—

Reaction Conditions

Temperature0 °C

Reaction Steps

600 mg (1.19 mmol) of methyl 2-[(t-butoxycarbonyl)amino]-4-[4-(5H-dibenzo[a,d][7]annulen-5-ylidene)-1-piperidinyl]-4-oxobutanoate was dissolved in 5 ml of ethyl acetate. 0.5 ml of 4 N hydrochloric acid/ethyl acetate solution was added to the obtained solution, and they were stirred at 0° C. for 3 hours. After stirring at room temperature overnight, the solvent was evaporated under reduced pressure. The residue was dissolved in 10 ml of dichloromethane. 602 mg (5.95 mmol) of triethylamine and 158 mg (1.31 mmol) of pivaloyl chloride were added to the obtained solution, and they were stirred for 10 minutes. Saturated aqueous sodium hydrogencarbonate solution and water were added to the reaction mixture. After extracting with ethyl acetate 3 times followed by the drying over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure, and the residue was purified by the silica gel chromatography (hexane:ethyl acetate=89:11 to 65:35) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462630B2
Source datasetuspto-grants-2008_12
ORD IDord-47d6415bbe204e7b979a1bdb4debeccc
Source noteuspto-grants-2008_12