関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| 反応物 | Potassium Fluoride | HCID 522689 | — |
| 反応物 | Methyl 2-bromothiazole-4-carboxylate | HCID 2763213 | — |
| 反応物 | 2,6-Difluoro-4-methoxybenzeneboronic acid | HCID 16217424 | — |
| 触媒 | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Methyl 2-(2,6-difluoro-4-methoxy-phenyl)thiazole-4-carboxylate | HCID 86713850 | 74% |
反応手順
To a solution of methyl 2-bromothiazole-4-carboxylate (3.27 mmol, 741 mg) in tetrahydrofuran (15 mL) and water (1.5 mL) was added 2,6-difluoro-4-methoxyphenylboronic acid (1.8 equiv., 5.88 mmol, 1160 mg) and potassium fluoride (3.3 equiv., 10.8 mmol, 627 mg). The mixture was degassed with nitrogen, then tris(dibenzylideneacetone)dipalladium(0) (0.2 equiv., 0.654 mmol, 617 mg) and tri-tert-butylphosphine (1.0 M in toluene; 0.4 equiv., 1.31 mmol, 1.3 mL) were added and the reaction mixture was heated under microwave at 100° C. for 30 minutes. The reaction mixture was concentrated and the residue was purified on silica eluted with 0 to 50% EtOAc in heptane to afford methyl 2-(2,6-difluoro-4-methoxy-phenyl)thiazole-4-carboxylate (2.40 mmol, 685 mg, 74% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09328106B2 |
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| 出典データセット | uspto-grants-2016_05 |
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| ORD ID | ord-0c202543724941d6853a27b6150abbbb |
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| 出典メモ | uspto-grants-2016_05 |
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