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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1929373생성일: 2026년 10월 27일

2-fluoro-N-methoxy-N,5-dimethylnicotinamide → Tert-butyl 4-(6-(2-fluoro-5-methylnicotinoyl)pyridin-2-yl)-1,4-diazepane-1-carboxylate

https://huagongshe.com/reaction/1929373

반응식

참여 물질

역할이름HCID투입량
반응물2-fluoro-N-methoxy-N,5-dimethylnicotinamideHCID 57690476—
반응물tert-Butyl 4-(6-bromopyridin-2-yl)-1,4-diazepane-1-carboxylateHCID 70700340—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 4-(6-(2-fluoro-5-methylnicotinoyl)pyridin-2-yl)-1,4-diazepane-1-carboxylateHCID 5769050187%

반응 조건

온도-78 °C

반응 단계

To a solution of tert-butyl 4-(6-bromopyridin-2-yl)-1,4-diazepane-1-carboxylate (898 mg, 2.52 mmol) in tetrahydrofuran (10 ml) at −78° C. was added a 2.5M solution of nbutyllithium in hexanes (1.01 ml, 2.52 mmol) dropwise maintaining the temperature at −78° C. After complete addition, the solution was stirred at −78° C. for a further 20 minutes. A solution of 2-fluoro-N-methoxy-N,5-dimethylnicotinamide (500 mg, 2.52 mmol) in tetrahydrofuran (5 ml) was added dropwise at −78° C. and the reaction mixture was stirred at −78° C. for 1 hour. The reaction was quenched with a saturated solution of ammonium chloride. The mixture was stirred at room temperature for 20 minutes and extracted into ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified on silica gel by flash column chromatography (ISCO Companion□, 40 g column, 0-20% EtOAc/Petrol) to afford the title compound as a sticky green oil (906 mg, 87% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08188071B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-5cfdfa8bc479410ba24d98435c04a36b
출처 메모uspto-grants-2012_05