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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352807Generated: October 29, 2026

3-Bromopyridine → HCID 22709894, compound

https://huagongshe.com/reaction/352807

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromopyridineHCID 12286—
Reactant5-(Trimethylstannyl)-1,3-thiazoleHCID 13662071—
CatalystHCID 178418397HCID 178418397—
SolventBenzeneHCID 241—
ProductHCID 22709894HCID 22709894—

Reaction Steps

At room temperature, tetrakis(triphenylphosphine)palladium (470 mg) was added to 3-bromopyridine (805 μl) and a solution of (5-thiazolyl)trimethyltin (2.07 g) in benzene (80 ml), followed by heating under reflux overnight. After the reaction mixture was allowed to cool down to room temperature, it was washed with a saturated aqueous solution (100 ml) of sodium bicarbonate. The water layer was extracted with ethyl acetate (3×20 ml). The organic layers were combine, dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column (hexane:ethyl acetate=2:1), whereby the title compound (1.68 g, purity: 85%) was obtained as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747023B1
Source datasetuspto-grants-2004_06
ORD IDord-ef91ef521d194eb6a9078ac078248d3e
Source noteuspto-grants-2004_06