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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432001Generated: October 26, 2026

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

https://huagongshe.com/reaction/432001

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 (1.37g) 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 numberUS06660753B2
Source datasetuspto-grants-2003_12
ORD IDord-00b2cad01a234d5f8a6cedebc4c801b5
Source noteuspto-grants-2003_12