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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1479504생성일: 2026년 10월 25일

Potassium Carbonate → 2-(Trifluoromethyl)benzo[f][1,7]naphthyridin-5-amine

https://huagongshe.com/reaction/1479504

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물3-Chloro-5-(trifluoromethyl)pyridine-2-carbonitrileHCID 1473374—
반응물(2-BOC-aminophenyl)boronic acidHCID 2773226—
용매MethanolHCID 887—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
생성물2-(Trifluoromethyl)benzo[f][1,7]naphthyridin-5-amineHCID 58213640—

반응 조건

온도100 °C

반응 단계

A solution of 2-(tert-butoxycarbonylamino)phenylboronic acid (1.0 eq.) and 3-chloro-5-(trifluoromethyl)picolinonitrile (from step 2) (1.0 eq.) in toluene (0.44 M) was mixed with tetrakis(triphenyl-phosphine)palladium (5 mol %) and 2N aqueous potassium carbonate solution (2.0 eq.). The reaction was heated to 100° C. and stirred overnight. After cooling to ambient temperature, the reaction content was diluted with 2% methanol in dichloromethane and water. The two phases were separated, and the aqueous layer was extracted twice with 2% methanol in dichloromethane. The combined organic layers were washed with brine, dried over anhydrous MgSO4, and concentrated en vacuo. The crude product was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-50% ethyl acetate in hexane to give 2-(trifluoromethyl)benzo[f][1,7]naphthyridin-5-amine. 1H NMR (acetone d-6): δ 9.44 (s, 1H), 9.20 (s, 1H), 8.65-8.63 (d, 1H), 7.70-7.61 (m, 2H), 7.44-7.36 (m, 1H), 6.84 (br, 2H). LRMS [M+H]=264.2

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09408907B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-92a6c5878e064c9f89d138e382a3a77e
출처 메모uspto-grants-2016_08