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HRID 2518作成日:2026年10月24日

Pyridine → 4-Trifluoroacetylamino-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(3-pyridyl)benzamide

https://huagongshe.com/ja/reaction/2518

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Trifluoroacetic acidHCID 6422—
反応物Sodium BicarbonateHCID 516892—
反応物4-amino-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(3-pyridyl)benzamideHCID 19690071—
溶媒DichloromethaneHCID 6344—
生成物4-Trifluoroacetylamino-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(3-pyridyl)benzamideHCID 1968992281.2%

反応手順

4-Amino-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(3-pyridyl)benzamide (229.3 mg, 0.51 mmol) was dissolved in methylene chloride (2.0 ml) to which were subsequently added pyridine (0.05 ml, 0.62 mmol) and anhydrous trifluoroacetic acid (0.09 ml, 0.64 mmol) at 0° C. After 3 hours of stirring at 0° C. to room temperature, the reaction solution was mixed with saturated sodium bicarbonate aqueous solution and extracted with chloroform. The resulting organic layer was washed with saturated sodium chloride aqueous solution and water in that order, and dried on anhydrous sodium sulfate. Thereafter, the solvent was removed by evaporation, and the resulting residue was purified by silica gel column chromatography (chloroform:methanol=20:1) to obtain 224.8 mg (81.2%) of the title compound in a light yellow powder form.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728835
出典データセットuspto-grants-1998_03
ORD IDord-83156c93ebe44f9b836d2b41d4fbb6ea
出典メモuspto-grants-1998_03