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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | SG 1842 | HCID 571799 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[2-(benzylamino)ethyl]pyridine-3-carboxamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04520027 |
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| Source dataset | uspto-grants-1985_05 |
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| ORD ID | ord-448be9d32d2b459a8a8e1094ca3b22c1 |
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| Source note | uspto-grants-1985_05 |
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