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HRID 340657作成日:2026年10月23日

2-Aminopyrimidine → 2-(4-Hydroxy-3-methoxyphenyl)imidazo[1,2-a]pyrimidine

https://huagongshe.com/ja/reaction/340657

反応式

関与物質

役割名称HCID仕込み量
反応物2-AminopyrimidineHCID 7978—
反応物2-Bromo-1-(4-hydroxy-3-methoxyphenyl)ethan-1-oneHCID 13542258—
溶媒AcetonitrileHCID 6342—
生成物2-(4-Hydroxy-3-methoxyphenyl)imidazo[1,2-a]pyrimidineHCID 6981045662.2%

反応条件

温度65 °C

反応手順

To 30 ml of an acetonitrile solution of 3.9 g (16 mmol) of 4′-hydroxy-3′-methoxy-2-bromoacetophenone was added 3.2 g (34 mmol) of 2-aminopyrimidine, and the mixture was stirred at 65° C. for 2 hours. The precipitated crystals were suction filtered and dissolved in 100 ml of 50% methanol. This solution was mixed with 1.3 g of sodium hydrogencarbonate and stirred at room temperature for 10 minutes. The precipitated crystals were suction filtered, and recrystallized from 50 ml of 50% methanol, thereby giving 2.4 g of 2-(4-hydroxy-3-methoxyphenyl)imidazo[1,2-a]pyrimidine in an yield of 62%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895599B2
出典データセットuspto-grants-2014_11
ORD IDord-59315116c28b4b959b943af348105111
出典メモuspto-grants-2014_11