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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20927생성일: 2026년 10월 24일

Acetonitrile → Carbonic Acid 17-(3-dioctadecylcarbamoyl-1-methyl-propyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester 2,5-dioxo-pyrrolidin-1-yl Ester

https://huagongshe.com/ko/reaction/20927

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물TriethylamineHCID 8471—
반응물Di(succinimido) carbonateHCID 676246—
반응물4-(3-Hydroxy-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-17-yl)-pentanoic Acid DioctadecylamideHCID 68638986—
용매DichloromethaneHCID 6344—
생성물Carbonic Acid 17-(3-dioctadecylcarbamoyl-1-methyl-propyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester 2,5-dioxo-pyrrolidin-1-yl EsterHCID 7226069671%

반응 단계

Referring to scheme 20, amide 82 (15.5 g, 17.6 mmol) was dissolved in anhydrous dichloromethane (150 mL). To the solution were added disuccinimidyl carbonate (6.76 g, 26.4 mmol), triethylamine (10 mL) and acetonitrile (50 mL). The reaction mixture was stirred at room temperature under argon for 6 h and then evaporated dryness. The residue was dissolved in dichloromethane (300 mL). It was washed with saturated NaHCO3 aqueous solution (3×100 mL). The organic layer was dried over Na2SO4, filtered and evaporated to dryness. Compound 83 (12.3 g, 71%) was obtained as colorless powder after drying in high vacuum, which was directly used for the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745608B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-1980ee76896d40ef85413b3f1947918a
출처 메모uspto-grants-2010_06