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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918552Generated: October 27, 2026

Hydrochloric Acid → 2-(2-(5-chloro-1H-indol-3-yl)ethylamino)-2-oxoacetic acid

https://huagongshe.com/reaction/1918552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantEthoxalyl chlorideHCID 20884—
Reactant5-Chloro-1H-indole-3-ethylamine monohydrochlorideHCID 2827494—
SolventDichloromethaneHCID 6344—
Product2-(2-(5-chloro-1H-indol-3-yl)ethylamino)-2-oxoacetic acidHCID 6683197581%

Reaction Steps

Triethylamine (2.28 mL; 16.22 mmol) was added to the mixture of 2-(5-chloro-1H-indol-3-yl)ethanamine hydrochloride (1.53 g; 6.49 mmol) and ethyl 2-chloro-2-oxoacetate (0.815 mL; 7.14 mmol) in dichloromethane (50 mL) at 0° C. After addition, the mixture was stirred at room temperature for 30 minutes and washed with an aqueous solution of sodium carbonate, dried over magnesium sulfate, and concentrated under reduced pressure. Ethanol (2 mL) and water (7.5 mL) were added to the resulting residue, followed by a 2M solution of sodium hydroxide (9.5 mL, 19 mmol). The mixture was stirred at room temperature for 20 minutes and the pH of the solution was adjusted to 1 by addition of a 6N hydrochloric acid. The precipitate was collected, and was dissolved in ethyl acetate. The ethyl acetate layer was dried over magnesium sulfate and was evaporated to dryness to give 1.36 g (81%) of 2-(2-(5-chloro-1H-indol-3-yl)ethylamino)-2-oxoacetic acid as a yellowish solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618138B2
Source datasetuspto-grants-2013_12
ORD IDord-5af011b93add433b9f32294fc16520b4
Source noteuspto-grants-2013_12