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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58565Generated: October 26, 2026

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

https://huagongshe.com/reaction/58565

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 numberUS09434722B2
Source datasetuspto-grants-2016_09
ORD IDord-a7d993b520b6444581f0b2e0f57d7396
Source noteuspto-grants-2016_09