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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2356802생성일: 2026년 10월 26일

Methanol → 3'-Fluoro-4'-[(6-fluoro-1,3-benzothiazol-2-yl)amino]-3-methylbiphenyl-4-carboxylic acid

https://huagongshe.com/reaction/2356802

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참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물WaterHCID 962—
반응물Sodium HydroxideHCID 14798—
반응물Methyl 3'-fluoro-4'-[(6-fluoro-1,3-benzothiazol-2-yl)amino]-3-methylbiphenyl-4-carboxylateHCID 59385264—
용매TetrahydrofuranHCID 8028—
생성물3'-Fluoro-4'-[(6-fluoro-1,3-benzothiazol-2-yl)amino]-3-methylbiphenyl-4-carboxylic acidHCID 59385254—

반응 조건

온도50 °C

반응 단계

As shown in Reaction Scheme 6, methyl 3′-fluoro-4′-[(6-fluoro-1,3-benzothiazol-2-yl)amino]-3-methylbiphenyl-4-carboxylate (0.38 g, 0.67 mmol) was suspended in THF (5 mL), MeOH (5 mL), and water (2.5 mL), and NaOH (0.27 g, 6.7 mmol) was added. The reaction mixture was heated at 50° C. for 3 h. Upon cooling to rt, the reaction mixture was concentrated in vacuo, acidified with 2N HCl, and the resulting solid was collected by filtration. This yielded 0.33 g (quantitative) of the title compound. 1H NMR (400 MHz, DMSO-d6) 2.62 (s, 3H), 7.10 (t, 1H), 7.49-7.58 (m, 5H), 7.65-7.75 (m, 1H), 8.10 (d, 1H), 8.58 (t, 1H), 10.85 (br, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07759376B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-d9ffd75ffa6a43cba58c75578b9e98da
출처 메모uspto-grants-2010_07