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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2-Bromobenzoyl chlorideHCID 23542—
Eduktmethyl((1-methyl-1H-indol-2-yl)methyl)amineHCID 11401058—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Bromo-N-methyl-N-[(1-methyl-1H-indol-2-yl)methyl]benzamideHCID 2272207887%

Reaktionsbedingungen

Temperatur0 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06730684B1
Quelldatensatzuspto-grants-2004_05
ORD IDord-9ddeb3f3465d40cf8fa45805d876cc1f
Quellennotizuspto-grants-2004_05