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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 69227Erstellt: 23. Oktober 2026

3-Bromo-6-chloroimidazo(1,2-b)pyridazine → (6-Chloroimidazo[1,2-b]pyridazin-3-yl)(5,7-difluoroquinolin-6-yl)methanol

https://huagongshe.com/de/reaction/69227

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Bromo-6-chloroimidazo(1,2-b)pyridazineHCID 12872323—
Edukt5,7-Difluoroquinoline-6-carbaldehydeHCID 57917282—
EduktHCID 178418443HCID 178418443—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(6-Chloroimidazo[1,2-b]pyridazin-3-yl)(5,7-difluoroquinolin-6-yl)methanolHCID 58147519—

Reaktionsschritte

3-Bromo-6-chloro-imidazo[1,2-b]pyridazine (4.40 g, 18.95 mmol) was dissolved THF (189 mL) and under nitrogen conditions, ethylmagnesium bromide solution (3 M, 6.32 mL) was added slowly. The RM was stirred at rt for 15 min then a solution of 5,7-difluoro-quinoline-6-carbaldehyde (Intermediate F, 3.66 g, 18.95 mmol) in THF was added. It was stirred at rt for 30 min. The reaction was quenched with 10% NH4Cl. The precipitate was filtered off and a first part of the title compound was obtained as a white solid. The filtrate was concentrated and was taken up with 10% NH4Cl. The precipitate was filtered off and was washed with EtOAc. A second part of the title compound was obtained as a brown solid (tR 0.8 min (conditions 2), MH+=347).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822468B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-5fab9e5c4ddf43969e95217a7e0db204
Quellennotizuspto-grants-2014_09