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HRID 420463作成日:2026年10月26日

Pyridine → 2-Pyridinecarboxamide

https://huagongshe.com/reaction/420463

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物O-PhenylenediamineHCID 7243—
反応物Picolinoyl Chloride HydrochlorideHCID 135033—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒Ethyl AcetateHCID 8857—
生成物2-PyridinecarboxamideHCID 1507060%

反応手順

Dissolving 5.0 g (17 mmol) of (4-bromo-phenyl)-(2-nitrophenyl)-amine into 50 milliliter of tetrahydrofuran, an aqueous solution prepared by dissolving 15 g (86 mmol) of sodium dithionite into 60 milliliter of water was added. Subsequently, adding 10 milliliter of methanol, the resultant solution was stirred at room temperature for 3 hours. After recognizing that the color (orange) of the resultant solution almost disappeared, water was added, followed by extracting with ethyl acetate. After sufficiently drying an organic layer with sodium sulfate, the solvent was removed by distillation, and as a result, phenylenediamine was obtained. Dissolving the resultant phenylenediamine into 150 milliliter of ethyl acetate, an organic layer was extracted. Further, 5.4 g (68 mmol) of pyridine, 3.6 g (23 mmol) of 2-picolinic acid chloride hydrochloride and catalyst amount of 4-dimethylaminopyridine (DMAP) were added to the organic layer, and the resultant solution was stirred at room temperature for 3 hours, followed by left standing for a night. After completion of the reaction, adding water, separation with filtration was carried out for precipitated solids and then, they were sufficiently washed with water and methanol, thereby obtaining 3.8 g of 2-picolinic acid amide as white solid (yield: 60%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08097349B2
出典データセットuspto-grants-2012_01
ORD IDord-ecbca9b7a3d24e138b1f1cf05f63770c
出典メモuspto-grants-2012_01