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HRID 219205Erstellt: 25. Oktober 2026

5-Chloro-2,3-difluoropyridine → 2,3-Difluoro-5-(3-methylisothiazol-5-yl)pyridine

https://huagongshe.com/reaction/219205

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Chloro-2,3-difluoropyridineHCID 2783248—
Edukt3-Methyl-5-(trimethylstannyl)isothiazoleHCID 10038320—
Edukt2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Katalysatorpalladium(II) acetateHCID 167845—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2,3-Difluoro-5-(3-methylisothiazol-5-yl)pyridineHCID 6750285898%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

5-chloro-2,3-difluoropyridine (0.069 ml, 0.67 mmol), X-Phos (0.045 g, 0.094 mmol) and palladium (II) acetate (0.011 g, 0.047 mmol) were combined in 1,4-dioxane (0.2 M, 3.4 mL). To the reaction vessel was added 3-methyl-5-(trimethylstannyl)isothiazole (0.53 g, 2.0 mmol) and, after purging with argon, the reaction was stirred at 100° C. for 2 h and then concentrated in vacuo. The crude material was dissolved in minimal DCM and purified via MPLC (eluting first with 100% EtOAc followed by 20% EtOAc in hexanes -isocratic) to yield 2,3-difluoro-5-(3-methylisothiazol-5-yl)pyridine (0.139 g, 98% yield) as a yellow solid. 2,3-difluoro-5-(3-methylisothiazol-5-yl)pyridine was converted to the title compound using a procedure similar to 1-(4-methyl-6-phenylpyridazin-3-yl)hydrazine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08198448B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-d2d3150d936c4ad4bfd41a0242e1af62
Quellennotizuspto-grants-2012_06