HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362793Generated: November 1, 2026
Triethylamine → N-Methoxy-N-methyl-1H-indole-3-carboxamide
https://huagongshe.com/reaction/362793
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Indole-3-Carboxylic Acid | HCID 69867 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-Methoxy-N-methyl-1H-indole-3-carboxamide | HCID 23299589 | 78% |
Reaction Steps
Indole-3-carboxylic acid (2.50 g, 0.0155 mol) was suspended in dichloromethane (60 ml) and treated with oxalyl chloride (1.62 ml, 0.0186 mol), followed by a drop of dry DMF. The reaction mixture was then stirred at room temperature overnight, before being evaporated under reduced pressure and dried in vacuo. The product was then redissolved in dichloromethane (50 ml) and added slowly to a solution of N,O-dimethylhydroxylamine hydrochloride (1.59 g, 0.0163 mol) in dichloromethane (50 ml) containing triethylamine (4.53 ml, 0.0326 mol) under argon. The resultant mixture was then stirred at room temperature for 2h, before being washed with water, followed by aq. NaHCO3. The organic layer was then dried (Na2SO4), evaporated under reduced pressure and dried in vacuo to yield the title compound as white solid (2.46 g, 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05872134 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-92f9fbce7d014f958801abf31ee7f2c4 |
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| Source note | uspto-grants-1999_02 |
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