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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710787Generated: November 1, 2026

Potassium Carbonate → Ethyl 2-(6-chloropyridin-3-yl)-4-methyl-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/1710787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-bromo-4-methyl-1,3-thiazole-5-carboxylateHCID 2824057—
Reactant2-Chloropyridine-5-boronic acidHCID 3845034—
CatalystHCID 178418397HCID 178418397—
SolventToluene ethanolHCID 21863594—
ProductEthyl 2-(6-chloropyridin-3-yl)-4-methyl-1,3-thiazole-5-carboxylateHCID 5945750169.1%

Reaction Steps

Ethyl 2-bromo-4-methyl-1,3-thiazole-5-carboxylate (1 g, 1.3 eq, 4 mmol) is added to a mixture of 2-chloro-5-pyridine boronic acid (0.48 g, 1 eq, 3.07 mmol), tetrakis(triphenylphosphine)palladium (0.18 g, 0.05 eq, 0.15 mmol) and an aqueous solution of 2 M potassium carbonate (3 ml, 2 eq, 6.14 mmol) in toluene/ethanol (18 ml, 2:1 v/v). The mixture is refluxed overnight and the solvent is evaporated, then taken up in ethyl acetate, and washed two times with an aqueous solution of sodium hydrogenocarbonate. The organic layer is dried over magnesium sulfate, filtered and concentrated under vacuum. Purification by chromatography over silicagel (eluent: dichloromethane 100%) affords 0.6 g of ethyl 2-(6-chloropyridin-3-yl)-4-methyl-1,3-thiazole-5-carboxylate i97.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790720B2
Source datasetuspto-grants-2010_09
ORD IDord-089c1b3c6cfb495f9c7494c438d9c2fb
Source noteuspto-grants-2010_09