関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methyl iodide | HCID 6328 | — |
| 反応物 | n-Butyl lithium | HCID 61028 | — |
| 反応物 | Acetone cardice | HCID 18522661 | — |
| 反応物 | (5-Cyclopropyl-isoxazol-3-yl)-carbamic acid phenyl ester | HCID 59394551 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (5-Cyclopropyl-4-methyl-isoxazol-3-yl)-carbamic acid phenyl ester | HCID 59394495 | — |
反応手順
(5-Cyclopropyl-isoxazol-3-yl)-carbamic acid phenyl ester (0.368 g, 1.51 mmol) is dissolved in THF (10 mL) and cooled to −78° C. and flushed with nitrogen. N-butyllithium (2.17 mL, 3.47 mmol) is then added. The mixture is stirred in the dry ice/acetone bath for 30 minutes. Methyl iodide (0.10 mL, 1.66 mmol) is added neat and the reaction is stirred for 2 hours at −78° C. The reaction is quenched (0° C.) with 20 mL of a saturated solution of ammonium chloride, diluted with ethyl acetate and the organic layer is removed, dried (sodium sulfate) and concentrated to an oil that is purified via FCC (0-40% ethyl acetate:heptanes) to give the title compound as an oil. MS (ESI) m/z 259.20 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08541432B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-7f3f3842e56e4a07967d61e5674b95f7 |
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| 出典メモ | uspto-grants-2013_09 |
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