関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Sodium Tartrate | HCID 9357 | — |
| 反応物 | N,O-Dimethylhydroxylamine | HCID 14232 | — |
| 反応物 | Trimethylaluminum | HCID 16682925 | — |
| 反応物 | 5-(3-Fluorophenylethynyl)-nicotinic acid ethyl ester | HCID 67047762 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | HCID 86622467 | HCID 86622467 | 33.2% |
反応手順
Sequentially add a 2 M solution of trimethylaluminum in toluene (0.64 g, 8.91 mmol) and 5-(3-fluorophenylethynyl)-nicotinic acid ethyl ester (0.24 g, 0.89 mmol), (prepared essentially as described in PREPARATION 17), to a solution of N,O-dimethylhydroxylamine (0.435 g, 4.46 mmol) in anhydrous toluene (4.0 mL) at 0° C. After 30 min, warm to room temperature and stir overnight. Dilute the reaction with ethyl acetate and an aqueous saturated solution of Rochelle salt (potassium sodium tartrate) and stir vigorously for 1 h. Separate the organic layer; dry (magnesium sulfate), filter and concentrate. Purify the resulting residue by silica gel chromatography, eluting with a linear gradient of 100:0 to 60:40 tetrahydrofuran:hexanes, to give the title compound as a pale yellow oil (0.084 g, 33%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07915424B2 |
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| 出典データセット | uspto-grants-2011_03 |
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| ORD ID | ord-587fed56830847d1b4748c7a75299f09 |
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| 出典メモ | uspto-grants-2011_03 |
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