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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1061819생성일: 2026년 10월 25일

5-chloro-2-(trifluoromethyl)-1,8-Naphthyridine → 6,2'-Difluoro-5'-(7-trifluoromethyl[1,8]naphthyridin-4-yl)biphenyl-3-carbonitrile

https://huagongshe.com/reaction/1061819

반응식

참여 물질

역할이름HCID투입량
반응물5-chloro-2-(trifluoromethyl)-1,8-NaphthyridineHCID 22285276—
반응물6,2'-Difluoro-5'-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)biphenyl-3-carbonitrileHCID 22285301—
생성물6,2'-Difluoro-5'-(7-trifluoromethyl[1,8]naphthyridin-4-yl)biphenyl-3-carbonitrileHCID 1015852527%

반응 단계

5-Chloro-2-trifluoromethyl[1,8]naphthyridine (50 mg, 0.22 mmol) was coupled to 6,2′-difluoro-5′-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)biphenyl-3-carbonitrile (96 mg, 0.28 mmol) as described in Example 7 part g), affording 6,2′-difluoro-5′-(7-trifluoromethyl[1,8]naphthyridin-4-yl)biphenyl-3-carbonitrile (24 mg, 27%). δH (400 MHz, CDCl3) 7.35 (1H, t, J 9.0), 7.45 (1H, t, J 9.0), 7.52-7.61 (3H, m), 7.74-7.78 (1H, m), 7.83 (1H, dd, J 1.4 and 6.5), 7.87 (1H, d, J 8.6), 8.54 (1H, d, J 8.2), 9.30 (1H, d, J 4.3). m/z (ES) 412 [MH]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06960598B2
출처 데이터셋uspto-grants-2005_11
ORD IDord-ea288886359e43ebb790636e458a1ef5
출처 메모uspto-grants-2005_11