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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353773Generated: October 30, 2026

3-Bromopyridine → HCID 178432533, compound

https://huagongshe.com/reaction/353773

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromopyridineHCID 12286—
ReactantHCID 23511456HCID 23511456—
ReactantHCID 178418443HCID 178418443—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178432533HCID 17843253388%

Reaction Steps

To a solution of 4-Iodo-3-methyl-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 3-bromopyridine (1.1 eq) were added to the reaction mixture. Subsequent reaction conditions were performed as in Example 91(b) to provide 3-(2-methyl-1H-imidazol-4-yl)-pyridine (88%) MH+(160).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756359B2
Source datasetuspto-grants-2004_06
ORD IDord-e5a14ecb3721444e97d6f9e9b994bb90
Source noteuspto-grants-2004_06