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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37210Generated: November 2, 2026

2-Aminopyridine → 2-Butylimidazo(1,2-a)pyridine

https://huagongshe.com/reaction/37210

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
Reactant1-Bromohexan-2-oneHCID 12431733—
SolventAcetoneHCID 180—
Product2-Butylimidazo(1,2-a)pyridineHCID 1512990753.1%

Reaction Steps

A mixture of 6 g of 2-amino pyridine and 60 ml of anhydrous acetone was added to a mixture of 16 g of the product of Stage B and 20 ml of acetone at ambient temperature. The mixture was refluxed for one hour and the acetone was partially distilled. The mixture was allowed to return to ambient temperature, ice-cooled, separated and washed with ethyl ether. The insoluble part was dissolved in a saturated solution of sodium carbonate and extraction was carried out with ethyl acetate. The extracts were washed with water saturated in sodium chloride, dried and filtered to obtain 5.9 g of the expected product in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420138
Source datasetuspto-grants-1995_05
ORD IDord-0a296b96e6cb4a569488c76c832ec44c
Source noteuspto-grants-1995_05