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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25516Erstellt: 24. Oktober 2026

Methyl iodide → [5-(1H-Indol-2-yl)-2-methoxy-phenyl]-methyl-amine

https://huagongshe.com/de/reaction/25516

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktPotassium CarbonateHCID 11430—
Edukt5-(1H-indol-2-yl)-2-methoxy-phenylamineHCID 9900204—
LösungsmittelAcetoneHCID 180—
Produkt[5-(1H-Indol-2-yl)-2-methoxy-phenyl]-methyl-amineHCID 992128827%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

In acetone (50 mL) was placed 5-(1H-indol-2-yl)-2-methoxy-phenylamine (2.38 g, 10 mmol). To this was added potassium carbonate (5.53 g, 40 mmol), and to the vigorously stirred mixture was added methyl iodide (1.55 g, 11 mmol). The mixture warmed to 40° C. and stirred for 48 hours. The mixture cooled to room temperature and was filtered free of inorganics. The resulting solution was evaporated in vacuo to give a solid which was partitioned between ethyl acetate (50 mL) and water (50 mL). The organic phase was separated, dried over magnesium sulfate, and evaporated in vacuo to give a tan solid. This solid was purified by flash chromatography over silica gel (5% ethyl acetate/methylene chloride). Evaporation of the appropriate fractions gave 0.68 g of pure compound. MS: M+1=253.1. 1H NMR (DMSO-d6) δ 2.79 (d, J=5.3 Hz, 3H), 3.80 (s, 3H), 5.08-5.12 (m, 1H), 6.69 (s, 1H), 6.83-7.05 (m, 5H), 7.33 (d, J=7.9 Hz, 1H), 7.44 (d, J=8.0 Hz, 1H), 11.28 (s, 1H) ppm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858739B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-5c508525b84f40e6abab25c56de6090c
Quellennotizuspto-grants-2005_02