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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465349Generated: October 30, 2026

Triethylamine → 3-{beta-(1-Ethyl-2-phenylimidazole-4-yl)acryloyl}amino-delta-valerolactam

https://huagongshe.com/reaction/465349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Aminopiperidin-2-oneHCID 19980260—
Reactantbeta-(1-Ethyl-2-phenylimidazole-4-yl)acrylate hydrochlorideHCID 70344434—
SolventTetrahydrofuranHCID 8028—
SolventThionyl ChlorideHCID 24386—
Product3-{beta-(1-Ethyl-2-phenylimidazole-4-yl)acryloyl}amino-delta-valerolactamHCID 54500275422.2%

Reaction Steps

β-(1-Ethyl-2-phenylimidazole-4-yl)acrylate hydrochloride (5.49 g, 20.3 mmole) was heated with stirring in thionyl chloride (50 ml) for 50 minutes. After excessive thionyl chloride was completely distilled off under reduced pressure, tetrahydrofuran (50 ml) and triethylamine (4.12 g, 40.7 mmole) were added and then 3-amino-δ-valerolactam (2.79 g, 24.4 mmole) was added to the mixture with cooling, followed by stirring at room temperature overnight. A sodium bicarbonate solution was added to the reaction mixture which was extracted with a chlorofolm-methanol mixed solvent. After drying over magnesium sulfate, the solvent was distilled off under reduced pressure. The residue was subjected to silica gel flash chromatography to obtain the titled compound (29 g, 62.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05153201
Source datasetuspto-grants-1992_10
ORD IDord-9afc9657b35444d38a2628ef6d566be9
Source noteuspto-grants-1992_10