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HRID 33883作成日:2026年10月24日

Hydrazinecarboxaldehyde → 4-(4-Pyridin-4-yl-4H-[1,2,4]triazol-3-yl)-phenol

https://huagongshe.com/ja/reaction/33883

反応式

関与物質

役割名称HCID仕込み量
反応物HydrazinecarboxaldehydeHCID 12229—
反応物Phosphorus pentachlorideHCID 24819—
反応物4-methoxy-N-(pyridin-4-yl)benzamideHCID 667611—
溶媒Phosphorus oxychlorideHCID 24813—
生成物4-(4-Pyridin-4-yl-4H-[1,2,4]triazol-3-yl)-phenolHCID 13637582455%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429665B2
出典データセットuspto-grants-2008_09
ORD IDord-7099241919154d8197daed4588a5ac33
出典メモuspto-grants-2008_09