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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379723Generated: October 27, 2026

Pyridine → 3-Acetylamino-2-benzoyl-6-chloro-1-(ethoxycarbonyl)indole

https://huagongshe.com/reaction/379723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
Reactant3-Amino-2-benzoyl-6-chloro-1-(ethoxycarbonyl)indoleHCID 18367833—
SolventDichloromethaneHCID 6344—
Product3-Acetylamino-2-benzoyl-6-chloro-1-(ethoxycarbonyl)indoleHCID 1836804154%

Reaction Steps

To a solution of 3-amino-2-benzoyl-6-chloro-1-(ethoxycarbonyl)indole (300 mg, 0.88 mmol; example 1, step 2) in a mixture of dichloromethane (10 ml) and pyridine (0.08 ml, 0.96 mmol) was added acetyl chloride (0.07 ml, 0.96 mmol). After stirring for 4 h, the mixture was partitioned between 10% aqueous citric acid (50 ml) and diethyl ether (100 ml). The organic extract was washed consecutively with water (50 ml), saturated sodium bicarbonate (50 ml), water (50 ml) and brine (50 ml). After drying (MgSO4) and removal of solvent, the crude product was purified by flash chromatography eluting with ethyl acetate/hexane (1:1) to afford 183 mg (54%) of the titled compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300363B1
Source datasetuspto-grants-2001_10
ORD IDord-2eedbdddd43344a7a0cec60b0c1f8e49
Source noteuspto-grants-2001_10