HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1581675Erstellt: 25. Oktober 2026
Triethylamine → 2-Bromo-N-methyl-N-[(1-methyl-1H-indol-2-yl)methyl]benzamide
https://huagongshe.com/reaction/1581675
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2-Bromobenzoyl chloride | HCID 23542 | — |
| Edukt | methyl((1-methyl-1H-indol-2-yl)methyl)amine | HCID 11401058 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2-Bromo-N-methyl-N-[(1-methyl-1H-indol-2-yl)methyl]benzamide | HCID 22722078 | 87% |
Reaktionsschritte
A solution of 2-bromobenzoyl chloride (1.85 g, 8.45 mmole) in CH2Cl2 (10 mL) was added dropwise to a solution of 1-methyl-2-(methylaminomethyl)indole (1.47 g, 8.45 mmole) and Et3N (3.6 mL, 25.8 mmole) in CH2Cl2 (50 mL) at 0° C. The reaction was stirred at 0° C. for 15 min, then was allowed to warm to RT. After 2 hr, the mixture was concentrated in vacuo, and the residue was diluted with H2O. The mixture was extracted with Et2O, and the combined Et2O layers were dried (MgSO4) and concentrated in vacuo. The oily residue was triturated with Et2O/petroleum ether to afford the title compound (2.6 g, 87%) as a white solid: MS (ES) m/e 357 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06730684B1 |
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| Quelldatensatz | uspto-grants-2004_05 |
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| ORD ID | ord-9ddeb3f3465d40cf8fa45805d876cc1f |
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| Quellennotiz | uspto-grants-2004_05 |
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