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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463521Generated: October 25, 2026

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

https://huagongshe.com/reaction/463521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSG 1842HCID 571799—
SolventEthanolHCID 702—
ProductN-[2-(benzylamino)ethyl]pyridine-3-carboxamideHCID 4242394—

Reaction Steps

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 extracted 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04520027
Source datasetuspto-grants-1985_05
ORD IDord-448be9d32d2b459a8a8e1094ca3b22c1
Source noteuspto-grants-1985_05