Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 730164생성일: 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/730164
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | (S)-(+)-N-(2,3-Epoxypropyl)phthalimide | HCID 719412 | — |
| 반응물 | 4-(4-Aminophenyl)morpholin-3-one | HCID 11194854 | — |
| 용매 | Water ethanol | HCID 19096565 | — |
| 생성물 | 2-((2R)-2-hydroxy-3-((4-(3-oxomorpholin-4-yl)phenyl)amino)propyl)-1H-isoindole-1,3(2H)-dione | HCID 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 heated under reflux for 14 hours (the precipitate dissolves; after some time, another precipitate is formed). 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 heated under reflux for 13 hours (the precipitate dissolves; after some time, another precipitate is formed). 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07582666B2 |
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| 출처 데이터셋 | uspto-grants-2009_09 |
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| ORD ID | ord-cb53efc2c0044de2ace87cb64d470dd5 |
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| 출처 메모 | uspto-grants-2009_09 |
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