反应详情

Bis(tri-t-butylphosphine)palladium(0) (4.38 mg, 0.00857 mmol) and 4-[4-bromo-5-(1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-1,2,4-triazol-3-yl)-2-thienyl]pyridine (0.075 g, 0.17 mmol) were combined in a dry round bottomed flask fitted with a stirbar and sealed with a septum. The flask was evacuated/refilled with nitrogen three times then a solution of 4-chlorobenzylzinc chloride in tetrahydrofuran (0.50M, 0.720 mL, 0.360 mmol) was added dropwise via a syringe. A nitrogen line was attached and the reaction was stirred at rt for 30 minutes, then at 60° C. for ˜2 hours. The reaction was cooled to rt, diluted with EtOAc and saturated ammonium chloride solution, then the mixture was transferred to a separatory funnel. The organic layer was separated and the aqueous layer was extracted twice more with EtOAc. The organics were combined, washed with bicarbonate solution, then brine, then dried over sodium sulfate. The mixture was filtered then evaporated in vacuo and the residue was purified by column chromatography on silica, elution 100% hexane to 100% EtOAc to afford the title compound as a light yellow oil. Yield 63 mg (76% yield). LCMS: (FA) ES+, 483, 485.

1. customfitted with a stirbar
2. customsealed with a septum
3. additionThe flask was evacuated/refilled with nitrogen three times
4. waitat 60° C. for ˜2 hours
5. temperatureThe reaction was cooled to rt
6. customthe mixture was transferred to a separatory funnel
7. customThe organic layer was separated
8. extractionthe aqueous layer was extracted twice more with EtOAc
9. washwashed with bicarbonate solution
10. dry with materialbrine, then dried over sodium sulfate
11. filtrationThe mixture was filtered
12. customthen evaporated in vacuo
13. customthe residue was purified by column chromatography on silica, elution 100% hexane to 100% EtOAc