Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1260621Erstellt: 23. Oktober 2026

Methyl iodide → 2-Ethyl-1H-pyrrolo(2,3-b)pyridine

https://huagongshe.com/de/reaction/1260621

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
Edukt2-Methyl-7-azaindoleHCID 583066—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
Produkt2-Ethyl-1H-pyrrolo(2,3-b)pyridineHCID 589377—

Reaktionsschritte

To a solution of 2-methyl-7-azaindole (1.32 g, 10 mmol) in dry diethyl ether (60 ml) at room temperature under an inert atmosphere is added n-BuLi (18.8 ml of a 1.6 M solution in hexanes, 30 mmol) followed by f-BuOK (2.24 g, 20 mmol). The reaction mixture is stirred at room temperature for 40 minutes and then cooled to −70° C. whereupon methyl iodide (1.25 ml, 20 mmol) is added dropwise. Stirring continues for a further 2 hours after which time, the reaction mixture is quenched with water (2 ml) and is allowed to slowly warm to room temperature. The cooled solution is poured onto water (200 ml), neutralized with 1N HCl and then extracted with diethyl ether (80 ml). The organic portion is washed with water (2×60 ml), dried (Na2SO4) and concentrated in vacuo to yield the titled compound as orange crystals. [MH+CH3CN]+=188)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08470848B2
Quelldatensatzuspto-grants-2013_06
ORD IDord-070eb6e881b445dea67fb75ec5436e14
Quellennotizuspto-grants-2013_06