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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067812Generated: November 3, 2026

Benzoyl chloride → Ethyl 5-benzamido-1-methyl-2-indolecarboxylate

https://huagongshe.com/reaction/1067812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantEthyl 5-amino-1-methyl-1H-indole-2-carboxylateHCID 11424506—
SolventPyridineHCID 1049—
ProductEthyl 5-benzamido-1-methyl-2-indolecarboxylateHCID 2119463852.5%

Reaction Steps

In 20 ml of pyridine was dissolved 0.80 g (3.67 mmol) of ethyl 5-amino-1-methyl-2-indolecarboxylate. While stirring at room temperature, 0.57 g (4.03 mmol) of benzoyl chloride was added to the solution. After stirring for 2 hours at 70° C., the reaction mixture was cooled to room temperature and then poured onto ice water. The mixture was then extracted three times with ethyl acetate. The combined extracts were washed with lN hydrochloric acid and then with saturated sodium hydrogencarbonate solution. After drying over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to give 0.62 g (52.5%) of ethyl 5-benzamido-1-methyl-2-indolecarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248772B1
Source datasetuspto-grants-2001_06
ORD IDord-9011464d1af742659b02ecd50cd0a914
Source noteuspto-grants-2001_06