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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Cyanophenylboronic acid | HCID 2734610 | — |
| Reactant | 2-Chloro-5-[(2-methyl-4-thiazolyl)ethynyl]pyridine | HCID 11564911 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Product | 2-{5-[(2-Methyl-1,3-thiazol-4-yl)ethynyl]pyridin-2-yl}benzonitrile | HCID 16662868 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08242143B2 |
|---|
| Source dataset | uspto-grants-2012_08 |
|---|
| ORD ID | ord-d77f33e9e84a471a8b60662de6eb024f |
|---|
| Source note | uspto-grants-2012_08 |
|---|