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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 79428Erstellt: 23. Oktober 2026

Potassium Carbonate → 3-((3-Cyclopropyl-4-nitro-1H-indazol-1-yl)methyl)-1-methylpyridin-2(1H)-one

https://huagongshe.com/de/reaction/79428

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktCyclopropylboronic acidHCID 2760897—
Edukt3-((3-bromo-4-nitro-1H-indazol-1-yl)methyl)-1-methylpyridin-2(1H)-oneHCID 67261313—
Katalysatorpalladium(II) acetateHCID 167845—
KatalysatorSodium 2'-(dicyclohexylphosphino)-2,6-dimethoxybiphenyl-3-sulfonateHCID 23677046—
Lösungsmittel1,4-Dioxane--water (1/1)HCID 21886435—
Produkt3-((3-Cyclopropyl-4-nitro-1H-indazol-1-yl)methyl)-1-methylpyridin-2(1H)-oneHCID 6726043383,8%

Reaktionsschritte

To a 50 mL pear shaped flask was added 4-dioxane/water (3.2 mL/0.6 mL). The flask was cooled in an ice/water bath before applying vacuum for 20 minutes. 3-((3-Bromo-4-nitro-1H-indazol-1-yl)methyl)-1-methylpyridin-2(1H)-one (0.55 g, 1.52 mmol), cyclopropylboronic acid (0.33 g, 3.79 mmol), sodium 2′-(dicyclohexylphosphino)-2,6-dimethoxybiphenyl-3-sulfonate (0.047 g, 0.091 mmol), palladium acetate (0.01 g, 0.4 mmol), and potassium carbonate (0.84 g, 6.07 mmol) were combined in a 25 mL round bottom flask and placed under vacuum. The degassed solvent mixture was added to the solid reagents and the flask was affixed with a condenser. The apparatus was evacuated and back filled with argon 5 times before heating at reflux under argon for 5 hours. The mixture was cooled to ambient temperature and filtered through a pad of Celite®. The filter cake was washed with ethyl acetate and water. The filtrate phases were separated and the aqueous phase was extracted with ethyl acetate 3 times. The combined organic extracts were washed with saturated sodium bicarbonate 3 times. The organic phase was concentrated under vacuum and dried under high vacuum to give 3-((-cyclopropyl-4-nitro-1H-indazol-1-yl)methyl)-1-methylpyridine-2(1H)-one as a beige solid (413 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841455B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-3e16bca523634c25bb9d39cba49681b2
Quellennotizuspto-grants-2014_09