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HRID 2039826Erstellt: 26. Oktober 2026

Potassium Carbonate → 5-Methoxy-1-phenyl-1H-pyrrolo[2,3-c]pyridine

https://huagongshe.com/reaction/2039826

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktIodobenzeneHCID 11575—
EduktAmmonium ChlorideHCID 25517—
Edukt5-methoxy-1H-pyrrolo[3,2-b]pyridineHCID 5324369—
KatalysatorCopper, bis(2,4-pentanedionato-O,O')-, (SP-4-1)-HCID 5363992—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt5-Methoxy-1-phenyl-1H-pyrrolo[2,3-c]pyridineHCID 6692219092,8%

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

To a mixture of 5-methoxy-1H-pyrrolo[2,3-c]pyridine (6.00 g, 40.5 mmol; cf. D. Mazéas et al., Heterocycles 50 (1999), 1065), copper(II) acetylacetonate (1.06 g, 4.05 mmol) and potassium carbonate (11.2 g, 81.0 mmol) in DMSO (63 ml) was added iodobenzene (4.99 ml, 44.6 mmol). The reaction mixture was stirred at 130° C. for 10 h. The mixture was then cooled to room temperature, and a solution of ammonium chloride (20% in water) was added. The mixture was filtered through celite and the filtrate extracted three times with EA. The organic layers were combined, dried over sodium sulfate, filtered and evaporated under reduced pressure. Column chromatography of the residue on silica gel (EA/HEP) gave 8.43 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08580813B2
Quelldatensatzuspto-grants-2013_11
ORD IDord-e243633102c74b388dd3499f3436c046
Quellennotizuspto-grants-2013_11