関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | 4-Chloro-6-fluoroquinoline | HCID 2736586 | — |
| 反応物 | n-(1-Ethyl-1h-pyrazol-4-yl)-2-(4-hydroxy-2-methoxyphenyl)acetamide | HCID 67305890 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | N-(1-ethylpyrazol-4-yl)-2-[4-(6-fluoroquinolin-4-yloxy)-2-methoxyphenyl]acetamide | HCID 24758982 | 61.6% |
反応手順
A mixture of 4-chloro-6-fluoroquinoline (0.11 g), N-(1-ethylpyrazol-4-yl)-2-(4-hydroxy-2-methoxyphenyl)acetamide (0.168 g), caesium carbonate (0.433 g) and DMF (3 ml) was stirred and heated to 120° C. for 2.5 hours. The solvent was evaporated and the residue was purified by column chromatography on silica using a solvent gradient of 100:0 to 93:7 of ethyl acetate and methanol as eluent. There was thus obtained the title compound (0.157 g); 1H NMR: (DMSOd6) 1.33 (t, 3H), 3.6 (s, 2H), 3.77 (s, 3H), 4.07 (q, 2H), 6.71 (d, 1H), 6.83 (m, 1H), 6.99 (d, 1H), 7.35 (d, 1H), 7.42 (s, 1H), 7.75 (m, 1H), 7.88 (s, 1H), 7.98 (m, 1H), 8.12 (m, 1H), 8.7 (d, 1H), 10.04 (s, 1H); Mass Spectrum: M+H+ 421.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07973164B2 |
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| 出典データセット | uspto-grants-2011_07 |
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| ORD ID | ord-72dafd750e2f4f008a7fd1778f1db86b |
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| 出典メモ | uspto-grants-2011_07 |
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