HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609846Generated: November 1, 2026
Potassium Carbonate → HCID 10425067, compound
https://huagongshe.com/reaction/1609846
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 22260391 | HCID 22260391 | — |
| Reactant | 2-(1H-Imidazol-2-yl)-1,3-thiazole | HCID 22260395 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10425067 | HCID 10425067 | 80.1% |
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
| 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-7e4e8a52306045a1bb986772891e10a3 |
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| Source note | uspto-grants-2006_01 |
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