Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642318Generated: October 30, 2026

Ethyl 2-chloroacetoacetate → Ethyl 4-methyl-2-(pyridin-3-yl)-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/642318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-chloroacetoacetateHCID 11858—
ReactantThionicotinamideHCID 737155—
SolventEthanolHCID 702—
ProductEthyl 4-methyl-2-(pyridin-3-yl)-1,3-thiazole-5-carboxylateHCID 61908870.2%

Reaction Steps

A mixture of thionicotinamide (10 g, 0.07 mol) and 2-chloro-3-oxo-butyric acid ethyl ester (10 mL, 0.07 mol) in ethanol (100 mL) was heated at refluxed for 20 h before it was cooled to room temperature and concentrated in vacuo. It was partitioned between ethyl acetate and saturated sodium bicarbonate, the organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with a gradient of ethyl acetate and hexanes to give the title compound as a yellow oil (12.2 g): MS: (+) m/z 249.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696223B2
Source datasetuspto-grants-2010_04
ORD IDord-2d61ae193ea34b16a3c6ac78bb520765
Source noteuspto-grants-2010_04