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HRID 74159作成日:2026年10月24日

Acetyl chloride → 2-methyl-1-(tetrahydropyran-4-yl)benzimidazole-5-carboxylic acid HCl salt

https://huagongshe.com/ja/reaction/74159

反応式

関与物質

役割名称HCID仕込み量
反応物Acetyl chlorideHCID 6367—
反応物1,4-Dioxane hydrochlorideHCID 20443148—
反応物3-Amino-4-((tetrahydropyran-4-yl)amino)benzoic acidHCID 54888048—
溶媒1,4-DioxaneHCID 31275—
生成物2-methyl-1-(tetrahydropyran-4-yl)benzimidazole-5-carboxylic acid HCl saltHCID 6749844593.1%

反応条件

温度10 °C

反応手順

3-Amino-4-((tetrahydropyran-4-yl)amino)benzoic acid (see Working Example 4-2) (90 g, 0.38 mol) was dissolved in dioxane (900 mL), and after cooling to 10° C., a solution of acetyl chloride (35.0 g, 0.45 mol) in dioxane (900 mL) was added dropwise over the course of 35 minutes. After heating to reflux with stirring for 2.5 h, another solution of acetyl chloride (15.8 g, 0.20 mol) in dioxane (200 mL) was added to the reaction solution, and this was further heated to reflux with stirring for 3 hours. Next, a 4N HCl dioxane solution (100 mL) was added, and after heating to reflux with stirring for 8 h, this was allowed to cool to room temperature, the solid obtained was filtered off and washed with hexane to yield the title compound (105 g, quant.) as a light purple solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829035B2
出典データセットuspto-grants-2014_09
ORD IDord-c529147e2378423195e9ae0159b4dc6e
出典メモuspto-grants-2014_09