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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66798Generated: October 25, 2026

Diethylethanolamine → N-Decyl-3-(3-[4-(2-[N,N-diethylamino]ethoxycarbonyl)-2-oxo-pyrrolidino]phenyl)propenamide

https://huagongshe.com/reaction/66798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylethanolamineHCID 7497—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantN-Decyl-3-[3-(4-carboxy-2-oxo-pyrrolidino)phenyl]propenamideHCID 53878346—
SolventTetrahydrofuranHCID 8028—
ProductN-Decyl-3-(3-[4-(2-[N,N-diethylamino]ethoxycarbonyl)-2-oxo-pyrrolidino]phenyl)propenamideHCID 53877985—

Reaction Steps

To a stirred solution of 829 mg. of N-decyl-3-(3-[4-carboxy-2-oxo-pyrrolidino]phenyl)propenamide in 25 ml. of tetrahydrofuran was added 357 mg. of carbonyldiimidazole. The mixture was heated under reflux for 10 minutes, and then 258 mg. of 2-(N,N-diethylamino)ethanol was added. The mixture was again heated under reflux for 10 minutes, and then an additional 258 mg. of 2-(N,N-diethylamino)ethanol was added. The mixture was heated under reflux for 15 minutes and then it was cooled to room temperature. The solvent was removed by evaporation in vacuo, and the residue was dissolved in 75 ml. of ethyl acetate. The ethyl acetate solution was washed successively with water, 1 N sodium hydroxide, water and saturated sodium chloride solution. The ethyl acetate solution was then dried using sodium sulfate, and the ethyl acetate was removed by evaporation in vacuo. The residue (960 mg.) was recrystallized from isopropyl ether giving 570 mg. of the title compound, m.p. 78°-80° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04343813
Source datasetuspto-grants-1982_08
ORD IDord-3857bd8cf78a4782ba6b7bc50758fb4c
Source noteuspto-grants-1982_08