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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006694Generated: October 27, 2026

2,3-Diaminopyridine → 8-Amino-3-acetyl-2-methylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1006694

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DiaminopyridineHCID 9956—
Reactant1-Chloro-2,4-pentanedioneHCID 14496856—
SolventEthanolHCID 702—
Product8-Amino-3-acetyl-2-methylimidazo[1,2-a]pyridineHCID 2267264915.7%

Reaction Steps

A mixture of 2,3-diaminopyridine (7 g, 64.1 mmol), 3-chloroacetylacetone (8.6 g, 64.1 mmol) in ethyl alcohol (80 ml) was refluxed for 9 hours. The solvent was removed under reduced pressure and the residue dissolved in methylene chloride. A sodium bicarbonate solution was added and the organic layer was separated. The aqueous layer was extracted twice with methylene chloride. The combined organic layer was dried and evaporated under reduced pressure. Chromatography of the residue on silica gel (methylene chloride:methanol, 100:5) gave a product which after recrystallisation from ethyl acetate gave 1.9 g (15%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06790960B2
Source datasetuspto-grants-2004_09
ORD IDord-38a461c60e1d4357bd3b2c6fa6275990
Source noteuspto-grants-2004_09