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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 340282생성일: 2026년 10월 25일

Sodium Carbonate → 8-Methyl-2-(p-tolylethynyl)benzo[f][1,7]naphthyridin-5-amine

https://huagongshe.com/reaction/340282

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물tert-Butyl (5-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamateHCID 46737997—
반응물3-Chloro-5-(p-tolylethynyl)picolinonitrileHCID 66875734—
촉매HCID 178418397HCID 178418397—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
용매Toluene ethanolHCID 21863594—
생성물8-Methyl-2-(p-tolylethynyl)benzo[f][1,7]naphthyridin-5-amineHCID 66875016—

반응 단계

A solution of 3-chloro-5-(p-tolylethynyl)picolinonitrile (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) (1.2 eq.), tetrakis(triphenylphosphine)palladium (10 mol %), and 2N sodium carbonate aqueous solution (4.0 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, and the aqueous layer was extracted with 2% MeOH in DCM twice. 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 8-methyl-2-(p-tolylethynyl)benzo[f][1,7]naphthyridin-5-amine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895577B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-f641a89745d4449ba5ee82e6f08021af
출처 메모uspto-grants-2014_11