HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609850Generated: October 25, 2026
Potassium Carbonate → HCID 10245416, compound
https://huagongshe.com/reaction/1609850
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Fluoro-6-(1h-imidazol-2-yl)pyridine | HCID 21919286 | — |
| Reactant | 3-Chloro-2-chloromethyl-5-methoxy-pyrazine | HCID 22260377 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10245416 | HCID 10245416 | 71% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06982268B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-2580b6d8a71b4b11bdc6defea9541f1e |
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| Source note | uspto-grants-2006_01 |
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