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HRID 219289作成日:2026年10月27日

Dimethylformamide → 2-Fluoro-5-(3-methylisoxazol-5-yl)pyridine

https://huagongshe.com/reaction/219289

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物2-(Dicyclohexylphosphino)biphenylHCID 2734216—
反応物3-Methyl-5-(tributylstannyl)isoxazoleHCID 2763255—
反応物5-Bromo-2-fluoropyridineHCID 2783168—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
生成物2-Fluoro-5-(3-methylisoxazol-5-yl)pyridineHCID 5801553054.5%

反応条件

温度90 °C

反応手順

A 48 mL tube was charged with 5-bromo-2-fluoropyridine (1.17 ml, 11.4 mmol), 3-methyl-5-(tributylstannyl)isoxazole (5.29 g, 14.2 mmol), cyclohexyl JohnPhos (0.398 g, 1.14 mmol), Pd2dba3 (0.312 g, 0.341 mmol), and DMF (12.4 ml, 159 mmol), flushed with argon, sealed, then heated at 90° C. for 16 hours. Additional 3-methyl-5-(tributylstannyl)isoxazole (5.29 g, 14.2 mmol) (2 g), Pd2 dba3 (0.312 g, 0.341 mmol), and cyclohexyl JohnPhos (0.398 g, 1.14 mmol) were added and the mixture was stirred at 90° C. for 10 more hours. This was concentrated and the brown residue was purified by MPLC, eluting with 15% ethyl acetate in hexanes isocratic. 2-fluoro-5-(3-methylisoxazol-5-yl)pyridine (1.1029 g, 54.5% yield) isolated as a light yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198448B2
出典データセットuspto-grants-2012_06
ORD IDord-05945d12f2a2422db148d935ab22bd5d
出典メモuspto-grants-2012_06