돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20906생성일: 2026년 10월 24일

Triethylamine → 2-(6-{2-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-pyrrolidin-1-yl}-6-oxo-hexyl)-isoindole-1,3-dione

https://huagongshe.com/ko/reaction/20906

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Chloroform methanolHCID 21584188—
반응물6-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-hexanoic Acid Pentafluorophenyl EsterHCID 59347289—
반응물5-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-pyrrolidin-3-olHCID 131728217—
용매DichloromethaneHCID 6344—
생성물2-(6-{2-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-pyrrolidin-1-yl}-6-oxo-hexyl)-isoindole-1,3-dioneHCID 131728216—

반응 조건

온도0 °C

반응 단계

Amine 38 (9.32 g, 22.2 mmol) and triethyl amine (4.55 g, 6.27 mL, 45 mmol) weres dissolved in anhydrous dichloromethane (20 mL) and cooled to 0° C. under argon. To that solution was added compound 43a (9.5 g, 22.2 mmol) at 0° C. The reaction mixture was brought to ambient temperature and stirred further. After 30 mins, disappearance of starting materials were ascertained by TLC. (10% MeOH/CHCl3). The reaction mixture was diluted with dichloromethane (100 mL) and washed with 5% NaOH solution (3×50 mL) followed by water and brine. The organic layer was dried over anhydrous sodium sulfate, filtered and evaporated to dryness. Upon purification over silica gel compound 44a was obtained as foamy white solid in good yield. (13.2 g, 89%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745608B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-6bca0d340ca246198db5246eb817d3c4
출처 메모uspto-grants-2010_06