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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428020Generated: October 26, 2026

p-Anisoyl chloride → Ethyl 3-(4-methoxybenzamido)-1H-indole-2-carboxylate

https://huagongshe.com/reaction/428020

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantTriethylamineHCID 8471—
ReactantEthyl 3-amino-1H-indole-2-carboxylateHCID 732887—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductEthyl 3-(4-methoxybenzamido)-1H-indole-2-carboxylateHCID 75136394.1%

Reaction Steps

To a solution of 3-amino-2-indolecarboxylic acid ethyl ester (500 mg, 2.45 mmol) and triethylamine (272 mg, 2.70 mmol) in methylene chloride (5 mL) was added anisoyl chloride (418 mg, 2.45 mmol). The resulting mixture was stirred for 18 h at room temperature. The reaction mixture was diluted with ethyl acetate and washed with water. The organic phase was washed with 1 N aqueous hydrochloric acid, dried (sodium sulfate), filtered, and concentrated in vacuo to provide a yellow solid. Recrystallization from hexane/ethyl acetate provided 780 mg (94%) of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313151B1
Source datasetuspto-grants-2001_11
ORD IDord-733b89533ee64034b26e3ebb33f90f79
Source noteuspto-grants-2001_11