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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 340280생성일: 2026년 10월 25일

Potassium Carbonate → Ethyl 4-((5-amino-8-methylbenzo[f][1,7]naphthyridin-2-yl)ethynyl)benzoate

https://huagongshe.com/reaction/340280

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물tert-Butyl (5-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamateHCID 46737997—
반응물Ethyl 4-((5-chloro-6-cyanopyridin-3-yl)ethynyl)benzoateHCID 66874947—
촉매HCID 178418397HCID 178418397—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
용매Toluene ethanolHCID 21863594—
생성물Ethyl 4-((5-amino-8-methylbenzo[f][1,7]naphthyridin-2-yl)ethynyl)benzoateHCID 66892072—

반응 단계

A solution of ethyl 4-((5-chloro-6-cyanopyridin-3-yl)ethynyl)benzoate (from the previous step) (1.0 eq.), tert-butyl 5-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylcarbamate (from Example 5/Step 2) (2.6 eq.), tetrakis(triphenylphosphine)palladium (10 mol %), and potassium carbonate (5.3 eq.) in toluene/ethanol (2:1, 0.2 M) was stirred at 100° C. overnight. After cooling to ambient temperature, the reaction mixture was diluted with 2% MeOH in DCM. The two phases were separated. The combined organic layers were washed with brine, dried over anhydrous MgSO4, and concentrated en vacuo. The crude material was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-40% ethyl acetate in toluene to give ethyl 4-((5-amino-8-methylbenzo[f][1,7]naphthyridin-2-yl)ethynyl)benzoate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895577B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-930f72a5de8a4b7b94746930ace82af4
출처 메모uspto-grants-2014_11