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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014323Generated: November 2, 2026

Morpholine → HCID 59441895, compound

https://huagongshe.com/reaction/1014323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantAcryloyl chlorideHCID 13140—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-methoxy-6-nitro-2,3-dihydro-1H-indoleHCID 59441656—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 59441895HCID 5944189554%

Reaction Steps

To a solution of 5-(methyloxy)-6-nitro-2,3-dihydro-1H-indole (1.0 g, 5.15 mmol) and polymer-bound diisopropyl ethylamine (4.20 g, 15.46 mmol) in dichloromethane (200 mL) was added acryloyl chloride (0.51 g, 5.67 mmol) via a dropwise addition. After stirring overnight at rt, the solids were removed by vacuum filtration and washed with dichloromethane. The filtrate was concentrated under reduced pressure, and stored under vacuum for several hours. A portion of the crude mixture (0.4 g, 1.61 mmol) was redissolved in absolute ethanol (25 mL) and to this was added morpholine (0.41 g, 4.84 mmol). After heating at 60° C. for 3 hr, the reaction was concentrated under reduced pressure and solids were recrystallized from ethyl acetate/hexanes to provide 5-(methyloxy)-1-[3-(4-morpholinyl)propanoyl]-6-nitro-2,3-dihydro-1H-indole (0.44 g, 54%). ESIMS (M+H)+=336.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981903B2
Source datasetuspto-grants-2011_07
ORD IDord-d68a144e9a48454d9764f9d26da617e7
Source noteuspto-grants-2011_07