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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775434Generated: October 31, 2026

Ethanol → 3-(2-Aminoethyl)-6-fluoro-5-methoxy-1H-indole-2-carboxylic acid

https://huagongshe.com/reaction/1775434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 616433HCID 616433—
SolventWaterHCID 962—
Product3-(2-Aminoethyl)-6-fluoro-5-methoxy-1H-indole-2-carboxylic acidHCID 616432—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 7-fluoro-6-methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-one (780 mg), ethanol (5.00 mL), and water (5.00 mL) was added potassium hydroxide (1.58 g), followed by stirring at 80° C. overnight. Potassium hydroxide (1.58 g) was added to the reaction mixture, followed by stirring at 100° C. for 6 hours. After cooling to room temperature, the solvent was evaporated under reduced pressure. The obtained residue was dissolved in water (10.0 mL), to the mixture was added acetic acid (3.00 mL), and the precipitated solid was collected by filtration and dried under reduced pressure to obtain 3-(2-aminoethyl)-6-fluoro-5-methoxy-1H-indole-2-carboxylic acid (607 mg) as a reddish brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260445B2
Source datasetuspto-grants-2016_02
ORD IDord-009a54eb703a47618c578a868e0d79cc
Source noteuspto-grants-2016_02