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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372697Generated: October 31, 2026

Triethylamine → HCID 17859427, compound

https://huagongshe.com/reaction/1372697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-benzyl-1H-indole-3-carboxylic acidHCID 33671—
ReactantOxalyl chlorideHCID 65578—
ReactantMethyl 2-(4-amino-3-chlorophenyl)acetateHCID 13616273—
SolventDichloromethaneHCID 6344—
ProductHCID 17859427HCID 1785942798.4%

Reaction Conditions

Temperature-15 °C

Reaction Steps

To a solution of 1-benzylindole-3-carboxylic acid (201.3 mg, 0.801 mmol) in methylene chloride (4.0 ml) was added oxalyl chloride (103.1 μl, 1.202 mmol) under stirring at −15° C. The reaction mixture was stirred at room temperature for 2.5 hours and then, distilled under reduced pressure to remove the solvent. The residue was dissolved in methylene chloride (4.0 ml) and to the resulting solution were added a solution of methyl 3-chloro-4-aminophenylacetate (167.9 mg, 0.841 mmol) in methylene chloride (4.0 ml) and triethylamine (0.35 ml, 2.523 mmol) under stirring at room temperature. The reaction mixture was stirred at room temperature for 18 hours. The reaction mixture was distilled under reduced pressure to remove the solvent. The residue was diluted with chloroform, washed with 1N HCl, dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent, whereby methyl 4-((1-benzyl-3-indolylcarbonyl)amino)-3-chlorophenylacetate (341.3 mg, 98%) was obtained. The 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-bd34bfa642f741d8a72bc6028498ce32
Source noteuspto-grants-2007_01