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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 66798Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/66798

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethylethanolamineHCID 7497—
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
EduktN-Decyl-3-[3-(4-carboxy-2-oxo-pyrrolidino)phenyl]propenamideHCID 53878346—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-Decyl-3-(3-[4-(2-[N,N-diethylamino]ethoxycarbonyl)-2-oxo-pyrrolidino]phenyl)propenamideHCID 53877985—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04343813
Quelldatensatzuspto-grants-1982_08
ORD IDord-3857bd8cf78a4782ba6b7bc50758fb4c
Quellennotizuspto-grants-1982_08