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Acetone, oxime → 3-(3-Methoxy-phenyl)-isoxazolo[5,4-b]pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetone, oxime | HCID 67180 | — |
| 反応物 | (2-Chloro-pyridin-3-yl)-(3-methoxy-phenyl)-methanone | HCID 10243711 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 3-(3-Methoxy-phenyl)-isoxazolo[5,4-b]pyridine | HCID 58928285 | 68% |
反応手順
Combine acetone oxime (3.1 g, 42.4 mmol) in dimethylformamide (15 mL) and add potassium t-butoxide (4.76 g, 42.4 mmol) and stir for 1 hour. Add (2-chloro-pyridin-3-yl)-(3-methoxy-phenyl)-methanone (8.40 g, 34 mmol) dissolved in dimethylformamide (10 mL) and stir at room temperature, overnight. Separate the product between water and ether and evaporate. Purify by column (silica) chromatography (10% ethyl acetate/dichloromethane) and then reflux in a mixture of 1:1 ethanol:5% aqueous hydrochloric acid. Work-up with 5% aqueous sodium hydroxide and ether and purify by flash chromatography (5% ethyl acetate in dichloromethane) to give the title compound (5.21 g, 68% Yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07253165B2 |
| 出典データセット | uspto-grants-2007_08 |
| ORD ID | ord-56ca29a7da0b451cac9253a580723fd2 |
| 出典メモ | uspto-grants-2007_08 |