Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | 3-Iodopyridine-2,6-diamine | HCID 476218 | — |
| Reactant | (5-Fluoro-2-propoxyphenyl)boronic acid | HCID 16217217 | — |
| Catalyst | 1,5-Diphenylpenta-1,4-dien-3-one;palladium | HCID 154270 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | HCID 57582324 | HCID 57582324 | 35.5% |
Reaction Steps
To a suspension of 3-iodopyridine-2,6-diamine (Preparation 44, 1.5 g, 6.38 mmol) in ethanol (5 ml) and water (5 ml) was added 5-fluoro-2-propoxyphenyl boronic acid (1.6 g, 8.10 mmol) and sodium carbonate (744 mg, 7.02 mmol), then the slurry was stirred for 10 minutes at room temperature under nitrogen. Palladium (0) bis(dibenzylideneacetone) (0.088 g, 0.153 mmol) and tri-tert-butyl phosphine (1M solution in toluene, 1.28 ml, 1.28 mmol) were added and the reaction was heated at 80° C. for 6 hours before concentrating in vacuo. The residue was taken up in ethyl acetate (100 ml) and washed with water (3×50 ml) then brine (50 ml) before drying over anhydrous MgSO4, filtering and concentrating in vacuo. The residue was purified by column chromatography eluting with 1:9 to 8:2 ethyl acetate:heptane to afford the title compound as a yellow foam (0.591 g, 35% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08134007B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-b4965e2b23a6489f98ceb7d36e2dc40f |
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| Source note | uspto-grants-2012_03 |
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