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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609850Generated: October 25, 2026

Potassium Carbonate → HCID 10245416, compound

https://huagongshe.com/reaction/1609850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-6-(1h-imidazol-2-yl)pyridineHCID 21919286—
Reactant3-Chloro-2-chloromethyl-5-methoxy-pyrazineHCID 22260377—
SolventDimethylformamideHCID 6228—
ProductHCID 10245416HCID 1024541671%

Reaction Conditions

Temperature45 °C

Reaction Steps

A mixture of 3-chloro-2-chloromethyl-5-methoxy-pyrazine (350 mg, 1.81 mmol), 2-fluoro-6-(1H-imidazol-2-yl)-pyridine (266 mg, 1.63 mmol) and K2CO3 (750 mg, 5.43 mmol) in DMF (10 mL) is stirred at 45° C. for 16 hours. On cooling, the reaction is quenched with saturated NH4Cl (3 mL) and extracted with DCM (3×20 mL). The combined organic layers are dried and solvent removed. PTLC (silica gel) separation (10% MeOH in DCM) gives 370 mg of 3-chloro-2-[2-(6-fluoro-pyridin-2-yl)-imidazol-1-ylmethyl]-5-methoxy-pyrazine as an oil. 1H NMR (CDCl3) 8.08–8.14 (m, 1H), 7.98(s, 1H), 7.81 (dd, 1H), 7.20 (s, 1H), 7.07 (s, 1H), 6.80 (dd, 1H), 6.02 (s, 2H), 3.98 (s, 3H) F. Synthesis of 2-[2-(6-Fluoro-pyridin-2-yl)-imidazol-1-ylmethyl]-5-methoxy-3-pyridin-2-yl-pyrazine (Compound 7)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982268B2
Source datasetuspto-grants-2006_01
ORD IDord-2580b6d8a71b4b11bdc6defea9541f1e
Source noteuspto-grants-2006_01