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HRID 41080作成日:2026年10月23日
(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/ja/reaction/41080
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | (S)-(+)-N-(2,3-Epoxypropyl)phthalimide | HCID 719412 | — |
| 反応物 | 4-(4-Aminophenyl)morpholin-3-one | HCID 11194854 | — |
| 溶媒 | Water ethanol | HCID 19096565 | — |
| 生成物 | 2-((2R)-2-hydroxy-3-((4-(3-oxomorpholin-4-yl)phenyl)amino)propyl)-1H-isoindole-1,3(2H)-dione | HCID 11516758 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08530505B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-0ae50bad8b584d56bbc35aa982d42625 |
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| 出典メモ | uspto-grants-2013_09 |
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