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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609846Generated: November 1, 2026

Potassium Carbonate → HCID 10425067, compound

https://huagongshe.com/reaction/1609846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22260391HCID 22260391—
Reactant2-(1H-Imidazol-2-yl)-1,3-thiazoleHCID 22260395—
SolventDimethylformamideHCID 6228—
ProductHCID 10425067HCID 1042506780.1%

Reaction Conditions

Temperature45 °C

Reaction Steps

A mixture of 2-chloromethyl-3,5-dimethoxy-pyrazine (140 mg, 0.74 mmol), 2-(1H-imidazol-2-yl)-thiazole (106 mg, 0.70 mmol) and K2CO3 (307 mg, 2.22 mmol) in DMF (10 mL) is stirred at 45° C. for 16 hours. On cooling, the reaction is quenched with saturated NH4Cl (5 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 170 mg of 3,5-dimethoxy-2-(2-thiazol-2-yl-imidazol-1-ylmethyl)-pyrazine as an oil. 1H NMR (CDCl3) 7.80 (d, 1H), 7.68 (s, 1H), 7.32 (d, 1H), 7.09 (s, 1H), 6.98 (s, 1H), 5.97 (s, 2H), 3.92 (s, 3H) 3.87 (s, 3H). E. 3-Chloro-2-[2-(6-fluoro-pyridin-2-yl)-imidazol-1-ylmethyl]-5-methoxy-pyrazine (Compound 6) 1. Preparation of 3-Chloro-5-methoxy-pyrazine-2-carbaldehyde

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982268B2
Source datasetuspto-grants-2006_01
ORD IDord-7e4e8a52306045a1bb986772891e10a3
Source noteuspto-grants-2006_01