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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1-ethyl-1H-indole-3-carboxylic acid | HCID 3697160 | — |
| Reactant | Methyl 2-(4-amino-3-chlorophenyl)acetate | HCID 13616273 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-chloro-4-((1-ethyl-3-indolylcarbonyl)amino)phenylacetate | HCID 17858879 | 88.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157487B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-c872d94476db4c6cbd0217771009689e |
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| Source note | uspto-grants-2007_01 |
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