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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1616072생성일: 2026년 10월 26일

(S)-tert-butyl 3-oxo-4-(pyridin-2-yl)butan-2-ylcarbamate → Tert-butyl 1-(6-fluoro-4-(3-methylpyridin-2-yl)-3-(pyridin-2-yl)quinolin-2-yl)ethylcarbamate

https://huagongshe.com/reaction/1616072

반응식

참여 물질

역할이름HCID투입량
반응물(S)-tert-butyl 3-oxo-4-(pyridin-2-yl)butan-2-ylcarbamateHCID 58318617—
반응물(2-Amino-5-fluorophenyl)(3-methylpyridin-2-yl)methanoneHCID 69673444—
촉매Sodium tetrachloroaurate dihydrateHCID 18949434—
용매IsopropanolHCID 3776—
생성물Tert-butyl 1-(6-fluoro-4-(3-methylpyridin-2-yl)-3-(pyridin-2-yl)quinolin-2-yl)ethylcarbamateHCID 67599683—

반응 단계

A solution of (2-amino-5-fluorophenyl)(3-methylpyridin-2-yl)methanone (0.29 g, 1.26 mmol), (S)-tert-butyl 3-oxo-4-(pyridin-2-yl)butan-2-ylcarbamate (0.366 g, 1.386 mmol), and sodium tetrachloroaurate(iii) dihydrate (0.025 g, 0.063 mmol) in 2-propanol (5.0 mL) was stirred at 80° C. for 24 h under an argon atmosphere, then at room temperature for an additional 48 h. The solution was purified by silica gel column chromatography eluting with a gradient of 10-40% EtOAc in hexane to afford tert-butyl 1-(6-fluoro-4-(3-methylpyridin-2-yl)-3-(pyridin-2-yl)quinolin-2-yl)ethylcarbamate as a dark solid: LC-MS (ESI) m/z 459.2 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08765768B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-1f1e2d5cffe2438a81af4ee358475eae
출처 메모uspto-grants-2014_07