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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1-cyclohexylmethyl-7-chloro-1H-indole-3-carboxylic acid | HCID 68674009 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Chloro-1-(cyclohexylmethyl)-1H-indole-3-carboxamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07763732B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-d3d88f9275d34e9f83923c752baed0ed |
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| Source note | uspto-grants-2010_07 |
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