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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609845Generated: October 31, 2026

Potassium Carbonate → 2-[2-(6-Fluoro-pyridin-2-yl)-imidazol-1-ylmethyl]-3,5-dimethoxy-pyrazine

https://huagongshe.com/reaction/1609845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-6-(1h-imidazol-2-yl)pyridineHCID 21919286—
ReactantHCID 22260391HCID 22260391—
SolventDimethylformamideHCID 6228—
Product2-[2-(6-Fluoro-pyridin-2-yl)-imidazol-1-ylmethyl]-3,5-dimethoxy-pyrazineHCID 1042582265%

Reaction Conditions

Temperature45 °C

Reaction Steps

A mixture of 2-chloromethyl-3,5-dimethoxy-pyrazine (115 mg, 0.61 mmol), 2-fluoro-6-(1H-imidazol-2-yl)-pyridine (98 mg, 0.60 mmol) and K2CO3 (250 mg, 1.81 mmol) in DMF (7 mL) is stirred at 45° C. for 16 hours. On cooling, the reaction is quenched with saturated NH4Cl (3 mL) and extracted with DCM (3×15 mL). The combined organic layers are dried and solvent removed. PTLC (silica gel) separation (10% MeOH in DCM) gives 123 mg of 2-[2-(6-fluoro-pyridin-2-yl)-imidazol-1-ylmethyl]-3,5-dimethoxy-pyrazine as an oil. LRMS calcd 315.30, found 316.20 (MH+). D. 3,5-Dimethoxy-2-(2-thiazol-2-yl-imidazol-1-ylmethyl)-pyrazinel (Compound 5)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982268B2
Source datasetuspto-grants-2006_01
ORD IDord-7b53c740dee24e158d2d6935faf4945a
Source noteuspto-grants-2006_01