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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diethylethanolamine | HCID 7497 | — |
| 반응물 | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| 반응물 | N-Decyl-3-[3-(4-carboxy-2-oxo-pyrrolidino)phenyl]propenamide | HCID 53878346 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-Decyl-3-(3-[4-(2-[N,N-diethylamino]ethoxycarbonyl)-2-oxo-pyrrolidino]phenyl)propenamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04296120 |
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| 출처 데이터셋 | uspto-grants-1981_10 |
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| ORD ID | ord-3179c198d5bd4b2b98f8680e15a37b7f |
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| 출처 메모 | uspto-grants-1981_10 |
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