Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzofuran-3-carboxamide | HCID 68239402 | — |
| Reactant | Methyl 6-bromo-3-methoxypyridine-2-carboxylate | HCID 70700803 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| Product | HCID 117771658 | HCID 117771658 | 91.2% |
Reaction Steps
To a stirring mixture of methyl 6-bromo-3-methoxypicolinate (200 mg, 0.81 mmol), 2-(4-fluorophenyl)-N-methyl-6-(N-methylmethylsulfonamido)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzofuran-3-carboxamide (408 mg, 0.81 mmol) and K2CO3 (146 mg, 1.06 mmol) in dioxane/H2O (4 mL/0.2 mL) was added Pd(dppf)Cl2 (20 mg) under N2 protection. The mixture was stirred at 60° C. for 5 h, and after concentrated in vacuo, the residue was extracted with EtOAc. The organic phase was washed with brine, dried over Na2SO4 and evaporated. The residue was purified by column chromatography (PE:EtOAc=2:1, then 1:1) to give the product of methyl 6-(2-(4-fluorophenyl)-3-(methylcarbamoyl)-6-(N-methylmethylsulfonamido)benzofuran-5-yl)-3-methoxypicolinate (400 mg, yield: 90%). 1H-NMR (CDCl3, 400 MHz) δ 7.88˜7.92 (m, 3H), 7.70 (d, J=8.8 Hz, 1H), 7.56 (s, 1H), 7.40 (d, J=8.8 Hz, 1H), 7.14 (t, J=8.8 Hz, 2H), 5.85 (d, J=3.2 Hz, 1H), 3.91 (s, 3H), 3.89 (s, 3H), 3.15 (s, 3H), 2.92 (d, J=4.8 Hz, 3H), 2.72 (s, 3H). MS (M+H)+: 542.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09364482B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-61c259ec66b44a70bd76ba625767a9b8 |
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| Source note | uspto-grants-2016_06 |
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