関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | Potassium cyclopropyltrifluoroborate | HCID 23697338 | — |
| 反応物 | Methyl 5-bromo-6-chloropicolinate | HCID 46311197 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 触媒 | Butyl-1-adamantylphosphine | HCID 68995490 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 6-Chloro-5-cyclopropyl-pyridine-2-carboxylic acid methyl ester | HCID 86674735 | 59% |
反応手順
To a mixture of palladium(II)acetate (17.9 mg, 79.8 μmol), butyl-1-adamantylphosphine (42.9 mg, 120 μmol), potassium cyclopropyltrifluoroborate (597 mg, 4.03 mmol) and cesium carbonate (3.9 g, 12.0 mmol) under an argon atmosphere was added a solution of 5-bromo-6-chloro-pyridine-2-carboxylic acid methyl ester (CAN 1214353-79-3, 1 g, 3.99 mmol) in toluene (25.2 ml) and water (2.8 mL) under an argon atmosphere. The reaction mixture was heated to 100° C. for 20 h, diluted with water (17.5 ml), poured onto 100 ml ice/brine and extracted with i-PrOAc (2×100 mL). The combined extracts were dried over sodium sulfate and concentrated in vacuo to give a yellow liquid. This crude material was purified by column chromatography (70 g SiO2, n-heptane/i-PrOAc 0-10% over 120 min) to give the title compound (497 mg, 59%) as yellow solid, MS (EI): m/e=212.0 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09290451B2 |
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| 出典データセット | uspto-grants-2016_03 |
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| ORD ID | ord-a7c2082eeffe4f3b81d5aaff5077f1d8 |
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| 出典メモ | uspto-grants-2016_03 |
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