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HRID 2088674作成日:2026年10月25日

Phosphorus oxychloride → 5-Chloro-7-(2,4-dichlorophenyl)-2-[1-(propan-2-yl)piperidin-4-yl][1,2,4]triazolo[1,5-c]pyrimidine

https://huagongshe.com/reaction/2088674

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphorus oxychlorideHCID 24813—
反応物Sodium BicarbonateHCID 516892—
反応物7-(2,4-Dichlorophenyl)-2-[1-(1-methylethyl)piperidin-4-yl][1,2,4]triazolo[1,5-c]pyrimidin-5(6H)-oneHCID 136104184—
触媒Benzyl triethylammonium chlorideHCID 66133—
生成物5-Chloro-7-(2,4-dichlorophenyl)-2-[1-(propan-2-yl)piperidin-4-yl][1,2,4]triazolo[1,5-c]pyrimidineHCID 58305977—

反応条件

温度120 °C

反応手順

530 mg (1.30 mmol) of 7-(2,4-dichlorophenyl)-2-[1-(1-methylethyl)piperidin-4-yl][1,2,4]-triazolo[1,5-c]pyrimidin-5(6H)-one were initially charged in phosphorus oxychloride (16 ml), and 1.19 g (5.22 mmol) of benzyltriethylammonium chloride were added. The mixture was then stirred at 120° C. for 2.5 h. The reaction mixture was poured onto saturated aqueous sodium bicarbonate solution (150 ml), and solid sodium bicarbonate was added until a pH of 7 had been reached. The mixture was extracted with dichloromethane (3×50 ml), and the combined organic phases were washed with water (50 ml), dried over magnesium sulfate and concentrated. This gave 502 mg (89% of theory) of the product as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08436003B2
出典データセットuspto-grants-2013_05
ORD IDord-5e3c396978ab475f8103556eab6cfa93
出典メモuspto-grants-2013_05