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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216891Generated: October 26, 2026

2-Bromopyridine → 2-(1-trityl-1H-imidazol-4-yl)pyridine

https://huagongshe.com/reaction/2216891

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
Reactant4-(Tributylstannyl)-1-tritylimidazoleHCID 11828117—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product2-(1-trityl-1H-imidazol-4-yl)pyridineHCID 2194268877.9%

Reaction Steps

The crude 4-tributylstannyl-1-trityl-1H-imidazole (1.37 g) in toluene (10 mL) was treated sequentially with 2-bromopyridine (0.33 mL, 3.43 mmol) and Pd(PPh3)4 (0.26 g, 0.23 mmol). The reaction mixture was heated at reflux under an argon atmosphere for 4 hours. After cooling, the reaction mixture was concentrated in vacuo. The residue was dissolved in chloroform (50 mL) and sequentially washed with aqueous saturated potassium fluoride (75 mL), water (75 mL) and brine (100 mL). The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated in-vacuo to afford 0.69 g of crude 4-(2-pyridyl)-1-trityl-1H-imidazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112595B2
Source datasetuspto-grants-2006_09
ORD IDord-5450ae1afaa74ac694af3e35d28c3907
Source noteuspto-grants-2006_09