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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 887148Erstellt: 25. Oktober 2026

Benzyl 2-(tributylstannyl)acrylate → Benzyl 2-(3-methyl[1,2,4]triazolo[4,3-a]pyridin-8-yl)acrylate

https://huagongshe.com/reaction/887148

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl 2-(tributylstannyl)acrylateHCID 66838741—
Edukt8-Bromo-3-methyl-[1,2,4]triazolo[4,3-A]pyridineHCID 66924502—
KatalysatorCuprous chlorideHCID 62652—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktBenzyl 2-(3-methyl[1,2,4]triazolo[4,3-a]pyridin-8-yl)acrylateHCID 6692447073%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a solution of 0.13 g (0.61 mmol) of 8-bromo-3-methyl[1,2,4]triazolo[4,3-a]pyridine from Step B above in 4 mL of anhydrous THF was added a solution of 0.36 g (0.80 mmol) of benzyl 2-(tributylstannyl)acrylate (see Intermediate 62, Step B) in 1 mL of anhydrous THF, 0.11 g (0.09 mmol) of tetrakis(triphenylphosphine)palladium(0) and 0.067 g (0.67 mmol) of copper (I) chloride. The reaction mixture was heated to 60° C. for 6 h, cooled and filtered through a pad of Celite®. The pad was washed with 15 mL of a dichloromethane and the combined filtrates were evaporated to dryness. The crude residue was purified by silica gel chromatography eluting with a 0-6% methanol in ethyl acetate gradient to afford the title compound (0.13 g, 73%). LC-MS: m/z (ES) 294 (MH)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08247415B2
Quelldatensatzuspto-grants-2012_08
ORD IDord-1b45fe5e038a4dd0917d21bd16cba2c8
Quellennotizuspto-grants-2012_08