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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 338444Erstellt: 25. Oktober 2026

Dimethylformamide → 6-chloro-5-(5-phenylpyrazin-2-yl)-1H-indole-3-carbaldehyde

https://huagongshe.com/reaction/338444

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktPotassium CarbonateHCID 11430—
EduktChloro-N,N-dimethylformiminium chlorideHCID 77311—
Edukt2-Chloro-5-phenylpyrazineHCID 1236664—
Edukt6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indoleHCID 86698733—
Produkt6-chloro-5-(5-phenylpyrazin-2-yl)-1H-indole-3-carbaldehydeHCID 86698775—

Reaktionsbedingungen

Temperatur30 °C

Reaktionsschritte

To a 0.4M solution of chlormethylene dimethylammonium chloride in DMF (7.5 mL, 3.8 mmol) was added 6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indole (493 mg, 1.88 mmol). The mixture was stirred at 30° C. for 2 hrs. 0.50 mL of this solution (0.15 mmol) was placed in a vial with a 0.3M solution of 2-chloro-5-phenylpyrazine in DMF (0.50 mL, 0.15 mmol). 2M potassium carbonate (0.30 mL, 0.60 mmol) was then added and the mixture purged with nitrogen. PddppfCl2 (9 mg, 0.01 mmol) was then added and the vial capped and heated to 90° C. for 3 hours. The reaction mixture was concentrated by Speedvac and purified via preparative TLC to give the title compound that was taken forward without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889730B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-90552355b19948d2b1ad3b1965bd6359
Quellennotizuspto-grants-2014_11