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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 848495생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/848495

반응식

참여 물질

역할이름HCID투입량
반응물DiethylethanolamineHCID 7497—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물N-Decyl-3-[3-(4-carboxy-2-oxo-pyrrolidino)phenyl]propenamideHCID 53878346—
용매TetrahydrofuranHCID 8028—
생성물N-Decyl-3-(3-[4-(2-[N,N-diethylamino]ethoxycarbonyl)-2-oxo-pyrrolidino]phenyl)propenamideHCID 53877985—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04296120
출처 데이터셋uspto-grants-1981_10
ORD IDord-3179c198d5bd4b2b98f8680e15a37b7f
출처 메모uspto-grants-1981_10