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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913913Generated: October 29, 2026

Potassium Carbonate → HCID 16662870, compound

https://huagongshe.com/reaction/1913913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Fluoro-2-methoxyphenylboronic acidHCID 2782673—
Reactant2-Chloro-5-[(2-methyl-4-thiazolyl)ethynyl]pyridineHCID 11564911—
CatalystHCID 178418476HCID 178418476—
ProductHCID 16662870HCID 16662870—

Reaction Conditions

Temperature80 °C

Reaction Steps

2-chloro-5-[(2-methyl-1,3-thiazol-4-yl)ethynyl]pyridine (1.0 mmol, 234 mg), 2-methoxy-5-fluorophenylboronic acid (2.0 mmol, 340 mg), dichlorobis(triphenylphosphine)palladium(II) (0.05 mmol, 35 mg), and potassium carbonate (3.5 mmol, 500 mg) were added to deoxygenated DME:water (1:1, 5 mL) at room temperature. The reaction was heated for 18 h at 80° C., then partitioned in a separatory funnel with EtOAc (100 mL) and water (30 mL). The organic layer was washed with one additional portion of water (20 mL) and the combined aqueous layers back extracted with EtOAc (50 mL). The combined organic layers were dried over MgSO4, filtered, and concentrated in vacuo. The crude residue was chromatographed on SiO2, eluting with a 0% to 60% EtOAc gradient in hexanes, to afford the title compound as a tan solid, which was dissolved in ether and precipitated as the hydrochloride salt with 1M HCl in ether. 1H-NMR (CD3OD, 500 MHz) δ 9.08 (s, 1H), 8.73 (d, 1H), 8.34 (d, 1H), 8.03 (s, 1H), 7.58 (dd, 1H), 7.45 (m, 1H), 7.33 (m, 1H), 3.97 (s, 3H), 2.77 (s, 3H). MS (ESI) 325.4 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609852B2
Source datasetuspto-grants-2013_12
ORD IDord-bb0b3789e6194bdfbc93dbb8f5f65583
Source noteuspto-grants-2013_12