돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40543생성일: 2026년 10월 24일

Triethylamine → N-[5-(3-fluoro-phenylethynyl)-pyridin-2-yl]-2-methoxy-2-methyl-propionamide

https://huagongshe.com/ko/reaction/40543

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-Fluoro-3-iodobenzeneHCID 70725—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물2-Methoxy-2-methyl-N-(5-trimethylsilanylethynyl-pyridin-2-yl)-propionamideHCID 86680825—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
용매TetrahydrofuranHCID 8028—
생성물N-[5-(3-fluoro-phenylethynyl)-pyridin-2-yl]-2-methoxy-2-methyl-propionamideHCID 7154834366.1%

반응 조건

온도70 °C

반응 단계

2-Methoxy-2-methyl-N-(5-trimethylsilanylethynyl-pyridin-2-yl)-propionamide (Example 13, step 2) (90 mg, 0.31 mmol) was dissolved in THF (8 ml). 1-Fluoro-3-iodobenzene (83 mg, 0.37 mmol, 1.2 equiv.), Et3N (130 μl, 0.93 mmol, 3 equiv.), bis-(triphenylphosphine)-palladium(II)dichloride (11 mg, 15 μmol, 0.05 equiv.) and copper(I)iodide (1.8 mg, 10 μmol, 0.03 equiv.) were added under nitrogen and the mixture was heated to 70° C. TBAF 1M in THF (370 μl, 0.37 mmol, 1.2 equiv.) was added dropwise at 70° C. The reaction mixture was stirred for 1 hour at 70° C., filtered through celite and the filtrate evaporated to dryness. The crude product was purified by flash chromatography with a silica gel column eluting with heptane:ethyl acetate 100:0->90:10. The desired N-[5-(3-fluoro-phenylethynyl)-pyridin-2-yl]-2-methoxy-2-methyl-propionamide (64 mg, 66% yield) was obtained as a yellow oil, MS: m/e=313.0 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530472B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-3f2aab5138514f34974511fae9fc787b
출처 메모uspto-grants-2013_09