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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386330Generated: October 31, 2026

2-Morpholinoethylamine → 5-(2-Morpholinoethylaminosulphonyl)oxindole

https://huagongshe.com/reaction/1386330

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MorpholinoethylamineHCID 408285—
Reactant2-oxo-2,3-dihydro-1H-indole-5-sulfonyl chlorideHCID 4962506—
SolventEthanolHCID 702—
Product5-(2-Morpholinoethylaminosulphonyl)oxindoleHCID 2171730354%

Reaction Conditions

Temperature65 °C

Reaction Steps

A solution of 5-chlorosulphonyloxindole (1 g, 4.3 mmol), (prepared as described for the starting material in Example 60), and 4-(2-aminoethyl)morpholine (620 μl, 4.7 mmol) in ethanol (20 ml) was heated at 65° C. for 1 hour. The solvent was removed by evaporation, the residue was partitioned between methylene chloride and water and the aqueous layer was adjusted to pH7-8 with 5% aqueous sodium hydrogen carbonate solution. The organic layer was separated, washed with brine, dried (MgSO4) and the solvent removed by evaporation. The residue was purified by column chromatography eluting with methylene chloride/methanol (95/5) to give 5-(2-morpholinoethylaminosulphonyl)oxindole (750 mg, 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265411B1
Source datasetuspto-grants-2001_07
ORD IDord-e1fa01c8a58441a5acca466ca14cb5fd
Source noteuspto-grants-2001_07