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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334730Generated: October 30, 2026

2-Bromo-6-(fluoromethyl)pyridine → HCID 66597939, compound

https://huagongshe.com/reaction/334730

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-6-(fluoromethyl)pyridineHCID 10241610—
ReactantHCID 86086898HCID 86086898—
ProductHCID 66597939HCID 66597939—

Reaction Steps

The title compound was prepared in accordance with the general method of Example 190(F), from 2-bromo-6-(fluoromethyl)pyridine (109 mg, 0.57 mol) and 2-(but-3-ynyl)-4,6-difluoro-1-methyl-1H-benzo[d]imidazole (126 mg, 0.57 mmol). The crude residue was purified over silicagel chromatography (prepacked 25 g silicagel column, DCM/MeOH: from 100/0 to 99/1 as eluent) to afford 43 mg of a light brown solid. The resulting solid was dissolved in Dioxane and 0.5N HCl in dioxan was added (0.14 mL, 0.07 mmol). A green solid was formed and it was collected by filtration and washed with AcOEt. The chlorhydrate salt was dissolved in MeOH, neutralized by saturated NaHCO3. The aqueous layer was extracted twice with AcOEt. The organic layer was dried over MgSO4 and the solvent removed under reduced pressure to afford 9 mg of 4,6-difluoro-2-(4-(6-(fluoromethyl)pyridin-2-yl)but-3-ynyl)-1-methyl-1H-benzo[d]imidazole (Yield: 5%) as purple oily solid (Mp=103° C.-104° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-aa3826729357403db577a6283c1ef09f
Source noteuspto-grants-2014_11