Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-6-iodopyridin-3-ol | HCID 10979479 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Bromo-6-iodo-3-methoxypyridine | HCID 11099040 | — |
Reaction Steps
To a solution of 2-bromo-3-hydroxy-6-iodopyridine (5-2, 40 g, 133 mmol) in DMF (80 ml) was added K2CO3 (16.77 g, 121 mmol) and methyl iodide (66.3 g, 467 mmol). The system was stirred for 45 minutes at 100° C., cooled to room temperature and then treated with water (650 mL) and stirred for 0.5 h. The resulting solids that precipitated from solution were isolated by filtration and dried to give the title compound (5-3) as a pale brown solid. ESI+MS C6H5BrINO: 313.8 found, 313.9 required.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08349872B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-049a14be832744d5b9956e4880309ab5 |
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| Source note | uspto-grants-2013_01 |
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