関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrazinecarboxaldehyde | HCID 12229 | — |
| 反応物 | Phosphorus pentachloride | HCID 24819 | — |
| 反応物 | 4-methoxy-N-(pyridin-4-yl)benzamide | HCID 667611 | — |
| 溶媒 | Phosphorus oxychloride | HCID 24813 | — |
| 生成物 | 4-(4-Pyridin-4-yl-4H-[1,2,4]triazol-3-yl)-phenol | HCID 136375824 | 55% |
反応手順
To a solution of 4-Methoxy-N-pyridin-4-yl-benzamide (75 mg) in POCl3 (3 ml) was added PCl5 (68 mg) and the reaction mixture heated at reflux for 5 h. The reaction mixture was concentrated and dissolved in dimethyl formamide (2 ml) and Formic acid hydrazide (5 eq, 100 mg) was added and stirred for 2 h. The reaction mixture was concentrated and diluted with isopropanol (3 mL) and 0.25 ml of conc. HCl was added. The reaction mixture stirred for 18 h, quenched with 1 NaOH, extracted with dichloromethane, dried magenesium sulfate and concentrated. The crude product dissolved in methylene chloride (2 mL) and boron tribromide (0.63 mL 1.0M hexanes) was added at 0° C. The reaction mixture was warmed to ambient temperature and stirred for 18 h. The reaction mixture was quenched with 1 N NaOH and pH adjusted to 9, extracted with dichloromethane, dried magnesium sulfate, filtered and concentrated. Purification via Biotage MPLC chromatography eluting with 0-20% methanol/methylene chlroride provided the title compound (32 mg, 55%). MS: (M+H m/z=239.2).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07429665B2 |
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| 出典データセット | uspto-grants-2008_09 |
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| ORD ID | ord-7099241919154d8197daed4588a5ac33 |
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| 出典メモ | uspto-grants-2008_09 |
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