HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386330Generated: October 31, 2026
2-Morpholinoethylamine → 5-(2-Morpholinoethylaminosulphonyl)oxindole
https://huagongshe.com/reaction/1386330
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Morpholinoethylamine | HCID 408285 | — |
| Reactant | 2-oxo-2,3-dihydro-1H-indole-5-sulfonyl chloride | HCID 4962506 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(2-Morpholinoethylaminosulphonyl)oxindole | HCID 21717303 | 54% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06265411B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-e1fa01c8a58441a5acca466ca14cb5fd |
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| Source note | uspto-grants-2001_07 |
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