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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275780Generated: October 30, 2026

Ethyl 2-chloroacetoacetate → Ethyl 8-(benzyloxy)-2-methylimidazo[1,2-A]pyridine-3-carboxylate

https://huagongshe.com/reaction/2275780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-chloroacetoacetateHCID 11858—
Reactant2-Amino-3-benzyloxypyridineHCID 90334—
SolventEthanolHCID 702—
ProductEthyl 8-(benzyloxy)-2-methylimidazo[1,2-A]pyridine-3-carboxylateHCID 44382335—

Reaction Conditions

Temperature100 °C

Reaction Steps

25 g of 2-amino-3-benzyloxypyridine (124.8 mmol, 1 equivalent) were dissolved in 781 ml of ethanol, and 102.7 g of ethyl 2-chloroacetoacetate (624.2 mmol, 5 equivalents) and 15 g of 4 Å molecular sieve were added. The mixture was heated at reflux for 2 d (bath temperature 100° C.). The mixture was then concentrated and excess ethyl 2-chloroacetoacetate was distilled off on a rotary evaporator with dry ice-cooling. The residue was purified by silica gel chromatography (mobile phase cyclohexane:ethyl acetate 9:1, 4:1). This gave 20.81 g of the title compound (54% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126998B2
Source datasetuspto-grants-2015_09
ORD IDord-3201e1dab2c7448dae1b0112daf3a1b6
Source noteuspto-grants-2015_09