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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 219289생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/219289

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물2-(Dicyclohexylphosphino)biphenylHCID 2734216—
반응물3-Methyl-5-(tributylstannyl)isoxazoleHCID 2763255—
반응물5-Bromo-2-fluoropyridineHCID 2783168—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
생성물2-Fluoro-5-(3-methylisoxazol-5-yl)pyridineHCID 5801553054.5%

반응 조건

온도90 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198448B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-05945d12f2a2422db148d935ab22bd5d
출처 메모uspto-grants-2012_06