Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243717Generated: October 25, 2026

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

https://huagongshe.com/reaction/243717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 2-(tributylstannyl)acrylateHCID 66838741—
Reactant8-Bromo-3-methyl-[1,2,4]triazolo[4,3-A]pyridineHCID 66924502—
CatalystCuprous chlorideHCID 62652—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl 2-(3-methyl[1,2,4]triazolo[4,3-a]pyridin-8-yl)acrylateHCID 6692447073%

Reaction Conditions

Temperature60 °C

Reaction Steps

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)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653260B2
Source datasetuspto-grants-2014_02
ORD IDord-a8df4fb96c7a4c609242c227343165f4
Source noteuspto-grants-2014_02