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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597558Generated: November 3, 2026

Chloride → HCID 22316663, compound

https://huagongshe.com/reaction/1597558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
Reactant4-(Tri-n-butylstannyl)thiazoleHCID 2763258—
ReactantHCID 22316646HCID 22316646—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 22316663HCID 2231666387.6%

Reaction Steps

To a stirred solution of 2-(4-bromophenyl)-1-[3-fluoro-4-(methylsulfonyl)phenyl]-4-trifluoromethyl-1H-imidazole (0.361 g, 0.78 mmol) in 1,4-dioxane (12 mL) was added 4-(tributylstannyl)thiazole (0.35 g, 0.94 mmol), lithiun chloride (0.083 g, 1.95 mmol), and tetrakis(triphenylphosphine)palladium(0) (0.090 g, 0.078 mmol) at room temperature under nitrogen. The mixture was heated at reflux temperature for 3 hours. After cooling, volatiles were removed by evaporation. The residue was redissolved in ethyl acetate (30 mL) and the whole washed with water and brine. After dried over MgSO4 and concentration in vacuo. The crude mixture was purified by flash chromatography eluting with hexane/ethyl acetate (3/1). The resulting solid was recrystallized from ethyl acetate-hexane to give the title compound (0.319 g, 87.6% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06294558B1
Source datasetuspto-grants-2001_09
ORD IDord-61f573b6fa1b4b28bdda5e9177009f36
Source noteuspto-grants-2001_09