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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353769Generated: October 30, 2026

4-Iodo-1-tritylimidazole → HCID 178505534, compound

https://huagongshe.com/reaction/353769

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Iodo-1-tritylimidazoleHCID 618252—
Reactant5-Bromo-2-fluoropyridineHCID 2783168—
ReactantHCID 178418443HCID 178418443—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178505534HCID 17850553446%

Reaction Steps

To a solution of 4-Iodo-1-trityl-1H-imidazole (1 eq) in THF at room temperature was added ethylmagnesium bromide (1.2 eq) under dry conditions. After stirring for 90 minutes, zinc chloride (1.2 eq) was added to the reaction mixture. After stirring for another 90 minutes, tetrakis(triphenylphosphine)palladium (10%) and 5-bromo-2-fluoropyridine (1.2 eq) were added to the reaction mixture. Subsequent reaction conditions and work up are as described previously, in Example 73 to afford the solid 2-Fluoro-5-(1H-imidazol-4-yl)-pyridine (46%). MH+(164).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756359B2
Source datasetuspto-grants-2004_06
ORD IDord-b50cd01093f94198a5b30cef4e152629
Source noteuspto-grants-2004_06