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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68468생성일: 2026년 10월 24일

(S)-(+)-N-(2,3-Epoxypropyl)phthalimide → 2-((2R)-2-hydroxy-3-((4-(3-oxomorpholin-4-yl)phenyl)amino)propyl)-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/ko/reaction/68468

반응식

참여 물질

역할이름HCID투입량
반응물(S)-(+)-N-(2,3-Epoxypropyl)phthalimideHCID 719412—
반응물4-(4-Aminophenyl)morpholin-3-oneHCID 11194854—
용매Water ethanolHCID 19096565—
생성물2-((2R)-2-hydroxy-3-((4-(3-oxomorpholin-4-yl)phenyl)amino)propyl)-1H-isoindole-1,3(2H)-dioneHCID 11516758—

반응 단계

A suspension of 2-[(2S)-2-oxiranylmethyl]-1H-isoindole-1,3(2H)-dione (A. Gutcait et al. Tetrahedron Asym. 1996, 7, 1641) (5.68 g, 27.9 mmol) and 4-(4-aminophenyl)-3-morpholinone (5.37 g, 27.9 mmol) in ethanol/water (9:1, 140 ml) is refluxed for 14 h (the precipitate dissolves, after some time again formation of a precipitate). The precipitate (desired product) is filtered off, washed three times with diethyl ether and dried. The combined mother liquors are concentrated under reduced pressure and, after addition of a second portion of 2-[(2S)-2-oxiranylmethyl]-1H-isoindole-1,3(2H)-dione (2.84 g, 14.0 mmol), suspended in ethanol/water (9:1, 70 ml) and refluxed for 13 h (the precipitate dissolves, after some time again formation of a precipitate). The precipitate (desired product) is filtered off, washed three times with diethyl ether and dried. Total yield: 10.14 g, 92% of theory.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822458B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-d7fb07ecdb1c478cb22023cf93ed5e08
출처 메모uspto-grants-2014_09