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HRID 1589201作成日:2026年10月27日

Benzaldehyde → N-[2-(benzylamino)ethyl]pyridine-3-carboxamide

https://huagongshe.com/reaction/1589201

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物SG 1842HCID 571799—
溶媒EthanolHCID 702—
生成物N-[2-(benzylamino)ethyl]pyridine-3-carboxamideHCID 4242394—

反応手順

A solution of N-(2-aminoethyl)pyridine-3-carboxamide (26.5 g.) and benzaldehyde (16.35 ml.) in ethanol (220 ml.) was kept for 48 hours. A small quantity of solid was removed by filtration. Sodium borohydride (6.1 g.) was then added to the filtrate which was stirred for 1 hour. Glacial acetic acid was then added cautiously until the solution was neutral. The solution was diluted with water (100 ml.) and basified with 2M sodium hydroxide. The mixture was extracted with ethyl acetate (3×200 ml.) and the extracts washed with saturated brine, dried (Na2SO4) and evaporated. The residue was purified by chromatography on a column of Florisil (200 g.), eluting with ethyl acetate, to yield N-[2-(benzylamino)ethyl]pyridine-3-carboxamide (29.5 g.) as a pale brown oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04568691
出典データセットuspto-grants-1986_02
ORD IDord-7a9c8347d88d4f9090754c71dd962048
出典メモuspto-grants-1986_02