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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68468Generated: October 25, 2026

(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/reaction/68468

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-(+)-N-(2,3-Epoxypropyl)phthalimideHCID 719412—
Reactant4-(4-Aminophenyl)morpholin-3-oneHCID 11194854—
SolventWater ethanolHCID 19096565—
Product2-((2R)-2-hydroxy-3-((4-(3-oxomorpholin-4-yl)phenyl)amino)propyl)-1H-isoindole-1,3(2H)-dioneHCID 11516758—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822458B2
Source datasetuspto-grants-2014_09
ORD IDord-d7fb07ecdb1c478cb22023cf93ed5e08
Source noteuspto-grants-2014_09