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HRID 730164作成日:2026年10月24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/730164

反応式

関与物質

役割名称HCID仕込み量
反応物(S)-(+)-N-(2,3-Epoxypropyl)phthalimideHCID 719412—
反応物4-(4-Aminophenyl)morpholin-3-oneHCID 11194854—
溶媒Water ethanolHCID 19096565—
生成物2-((2R)-2-hydroxy-3-((4-(3-oxomorpholin-4-yl)phenyl)amino)propyl)-1H-isoindole-1,3(2H)-dioneHCID 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 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07582666B2
出典データセットuspto-grants-2009_09
ORD IDord-cb53efc2c0044de2ace87cb64d470dd5
出典メモuspto-grants-2009_09