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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566257Generated: November 2, 2026

2-Aminopyridine → HCID 21265805, compound

https://huagongshe.com/reaction/566257

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 21265818HCID 21265818—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 21265805HCID 2126580526.9%

Reaction Steps

4-Nitrobenzyl 4-bromo-3-oxopentanoate (1.02 g) and 2-aminopyridine (436 mg) were dissolved in 1,2-dimethoxyethane (20 ml). The solution was heated for 15 hours under reflux. The reaction mixture was concentrated, to which were added 1N HCl (10 ml) and ethyl acetate (10 ml). The mixture was shaken and left standing to form two layers. To the aqueous layer was added sodium hydrogencarbonate to adjust its pH to 7, followed by extraction with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, which was concentrated under reduced pressure. The concentrate was purified by means of a column chromatography (carrier: silica gel, 30 g, developing: ethyl acetate) to afford the title compound (0.27 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174877B1
Source datasetuspto-grants-2001_01
ORD IDord-850ab57f328641c18d7cc17303b27973
Source noteuspto-grants-2001_01