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HRID 395790作成日:2026年10月26日

Pyridine → N-(4-methoxyphenyl)-2-[[1-(4-pyridyl)piperidin-4-ylcarbonyl]amino]benzamide

https://huagongshe.com/reaction/395790

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Thionyl ChlorideHCID 24386—
反応物2-amino-N-(4-methoxyphenyl)benzamideHCID 478820—
反応物1-(Pyridin-4-yl)piperidine-4-carboxylic acidHCID 1268289—
溶媒DichloromethaneHCID 6344—
生成物N-(4-methoxyphenyl)-2-[[1-(4-pyridyl)piperidin-4-ylcarbonyl]amino]benzamideHCID 1817454530.2%

反応手順

To a stirred suspension of N-(4-pyridyl)isonipecotic acid (0.2 g, 1 mmol) in dichloromethane (70 mL) was added thionyl chloride (0.11 mL, 1.5 mmol). After stirring overnight, the solvent was removed in vacuo and the residue was dissolved in dichloromethane (10 mL) and added to a stirred solution of 2-amino-N-(4-methoxyphenyl)benzamide (0.186 g, 0.77 mmol) and pyridine (0.19 g, 0.85 mmol) in dichloromethane (25 mL). After stirring for 72 h, the solution was transferred to a separatory funnel and washed with water, saturated aqueous sodium bicarbonate solution, and saturated aqueous sodium chloride solution. The organic phase was dried (magnesium sulfate), filtered, and concentrated in vacuo. The residue was suspended in a mixture of diethyl ether and hexanes, sonicated, and filtered. The resulting solid was washed with diethyl ether and dried in vacuo to give 0.10 g (30%) of the title compound as a pale tan solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06605626B2
出典データセットuspto-grants-2003_08
ORD IDord-7ac8badbfd9c4996afebd2dc23dd7fda
出典メモuspto-grants-2003_08