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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1061820생성일: 2026년 10월 27일

5-chloro-2-(trifluoromethyl)-1,8-Naphthyridine → 5-(4-Fluoro-3-methoxyphenyl)-2-trifluoromethyl[1,8]naphthyridine

https://huagongshe.com/reaction/1061820

반응식

참여 물질

역할이름HCID투입량
반응물5-chloro-2-(trifluoromethyl)-1,8-NaphthyridineHCID 22285276—
반응물2-(4-Fluoro-3-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 22285305—
생성물5-(4-Fluoro-3-methoxyphenyl)-2-trifluoromethyl[1,8]naphthyridineHCID 994500883%

반응 단계

5-Chloro-2-trifluoromethyl[1,8]naphthyridine (923 mg, 4.0 mmol) was coupled to 2-(4-fluoro-3-methoxyphenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (1.30 g, 5.2 mmol) as described in Example 3 part g), affording 5-(4-fluoro-3-methoxyphenyl)-2-trifluoromethyl[1,8]naphthyridine (1.06 g, 83%). δH (360 MHz, CDCl3) 3.95 (3H, s), 6.99-7.04 (1H, m), 7.06 (1H, dd, J 7.7 and 2.1), 7.30 (1H, dd, J 2.5 and 8.4), 7.56 (1H, d, J 4.2), 7.82 (1H, d, J 8.4), 8.52 (1H, d, J 8.4), 9.27 (1H, d, J 4.2). m/z (ES+) 323 [MH]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06960598B2
출처 데이터셋uspto-grants-2005_11
ORD IDord-1a882e93ca4545bc900ff85dfc2f0027
출처 메모uspto-grants-2005_11