戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 68994作成日:2026年10月25日

4-Pyridinecarboxaldehyde → (2-Pyridin-3-ylethyl)pyridin-4-ylmethylamine

https://huagongshe.com/reaction/68994

反応式

関与物質

役割名称HCID仕込み量
反応物4-PyridinecarboxaldehydeHCID 13389—
反応物2-(Pyridin-3-yl)ethan-1-amineHCID 854051—
反応物Sodium borohydrideHCID 4311764—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物(2-Pyridin-3-ylethyl)pyridin-4-ylmethylamineHCID 60761584—

反応手順

4-Pyridine carbaldehyde (5.36 g) and 3-(2-aminoethyl)pyridine (6.5 ml) were added to 100 ml of methanol. The mixture was stirred at room temperature for 7 hours. The mixture was cooled to 0° C., and sodium borohydride (2.8 g) was added thereto. The mixture was further stirred at 0° C. for an hour. Water was added to the reaction mixture and methanol was distilled off under reduced pressure. The residue was subjected to extraction using dichloromethane. The organic layer was washed with saturated saline, dried with anhydrous sodium sulfate, and was condensed under reduced pressure. The residue was purified by basic silica gel column chromatography (ethyl acetate:methanol=95:5→85:5). The purified product was condensed under reduced pressure to give the title compound (10.03 g) as a colorless oily matter.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822453B2
出典データセットuspto-grants-2014_09
ORD IDord-d4f48387114947c59fea3f727a7bc9b3
出典メモuspto-grants-2014_09