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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712929Generated: October 31, 2026

Ethyl 2-bromothiazole-5-carboxylate → Ethyl 2-pyridin-2-yl-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/1712929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-bromothiazole-5-carboxylateHCID 3614103—
ReactantHCID 178419760HCID 178419760—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 2-pyridin-2-yl-1,3-thiazole-5-carboxylateHCID 53403816—

Reaction Steps

A mixture of bromo(pyridine-2-yl)zinc (0.5 M in THF, 1.27 mL), ethyl 2-bromo-1,3-thiazole-5-carboxylate (0.063 mL, 0.42 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.02 g, 0.02 mmol) in 1,4-dioxane (3 mL) and water (0.03 mL) was subjected to MWI at 120° C. for 10 min. The reaction mixture was diluted with water and extracted with EtOAc. The organic solutions were combined, dried over Na2SO4, filtered, and concentrated to give ethyl 2-pyridin-2-yl-1,3-thiazole-5-carboxylate (0.12 g) which was used without further purification. LCMS: (FA) ES+ 235.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795249B2
Source datasetuspto-grants-2010_09
ORD IDord-18b9ee07fd114b68b8cf1707eaaa6374
Source noteuspto-grants-2010_09