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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885030Generated: October 31, 2026

Potassium Carbonate → 2-{5-[(2-Methyl-1,3-thiazol-4-yl)ethynyl]pyridin-2-yl}benzonitrile

https://huagongshe.com/reaction/885030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Cyanophenylboronic acidHCID 2734610—
Reactant2-Chloro-5-[(2-methyl-4-thiazolyl)ethynyl]pyridineHCID 11564911—
CatalystHCID 178418476HCID 178418476—
Product2-{5-[(2-Methyl-1,3-thiazol-4-yl)ethynyl]pyridin-2-yl}benzonitrileHCID 16662868—

Reaction Conditions

Temperature150 °C

Reaction Steps

2-chloro-5-[(2-methyl-1,3-thiazol-4-yl)ethynyl]pyridine (1.0 mmol, 234 mg), 2-cyanophenylboronic acid (1.2 mmol, 176 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 5 min at 150° C. via microwave irradiation, 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 white solid, which was dissolved in ether and precipitated as the hydrochloride salt with 1M HCl in ether. MS (ESI) 301.4 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242143B2
Source datasetuspto-grants-2012_08
ORD IDord-d77f33e9e84a471a8b60662de6eb024f
Source noteuspto-grants-2012_08