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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372689Generated: October 31, 2026

Triethylamine → Methyl 3-chloro-4-((1-ethyl-3-indolylcarbonyl)amino)phenylacetate

https://huagongshe.com/reaction/1372689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant1-ethyl-1H-indole-3-carboxylic acidHCID 3697160—
ReactantMethyl 2-(4-amino-3-chlorophenyl)acetateHCID 13616273—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-chloro-4-((1-ethyl-3-indolylcarbonyl)amino)phenylacetateHCID 1785887988.4%

Reaction Conditions

Temperature15 °C

Reaction Steps

To 1-ethylindole-3-carboxylic acid (160.2 mg, 0.847 mmol) were added methylene chloride (3.5 ml) and oxalyl chloride (108.9 μl, 1.270 mmol) under stirring at 15° C. The reaction mixture was stirred for 2.5 hours at room temperature. The solvent was then distilled off under reduced pressure. To the residue was added methylene chloride (3.5 ml). Under stirring at room temperature, a solution of methyl 3-chloro-4-aminophenylacetate (177.5 mg, 0.889 mmol) in methylene chloride (3.5 ml) and triethylamine (0.37 ml, 2.667 mmol) were added and the mixture was heated under reflux for 18 hours. After the reaction mixture was cooled to room temperature, the solvent was distilled off under reduced pressure. The residue was dissolved in chloroform. The resulting solution was washed with 1N HCl ad saturated saline, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to give methyl 3-chloro-4-((1-ethyl-3-indolylcarbonyl)amino)phenylacetate (277.7 mg, 88%) as a brown amorphous substance. The resulting compound was provided for the subsequent reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-c872d94476db4c6cbd0217771009689e
Source noteuspto-grants-2007_01