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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358458Generated: October 31, 2026

Ammonia → 7-Chloro-1-(cyclohexylmethyl)-1H-indole-3-carboxamide

https://huagongshe.com/reaction/2358458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPotassium CarbonateHCID 11430—
ReactantOxalyl chlorideHCID 65578—
Reactant1-cyclohexylmethyl-7-chloro-1H-indole-3-carboxylic acidHCID 68674009—
SolventDichloromethaneHCID 6344—
Product7-Chloro-1-(cyclohexylmethyl)-1H-indole-3-carboxamideHCID 68675095—

Reaction Steps

Oxalyl chloride (4.95 g, 39.0 mmol) was added dropwise to a mixture of 7-chloro-1-(cyclohexyl)methyl-1H-indole-3-carboxylic acid (6.4 g, 21.9 mmol) and dichloromethane (150 ml) under ice-water cooling and the resulting mixture was stirred at room temperate for 20 h. Dichloromethane and excess oxalyl chloride were removed by evaporation and the obtained residue was mixed with dichloromethane (100 ml). Aqueous ammonia (33%, 50 ml) and potassium carbonate (6.05 g, 43.8 mmol) was added into the mixture under ice-water bath cooling. After stirring at room temperature for 2 h, the reaction mixture was concentrated in vacuo, then the obtained solid was washed with water, then n-heptane, and dried under reduced pressure to afford 7-chloro-1-(cyclohexyl)methyl-1H-indole-3-carboxylic acid amide (6.4 g, 22.0 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763732B2
Source datasetuspto-grants-2010_07
ORD IDord-d3d88f9275d34e9f83923c752baed0ed
Source noteuspto-grants-2010_07