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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77699생성일: 2026년 10월 24일

Sodium Hydroxide → 4-methyl-3-(9H-pyrimido[4,5-b]indol-7-yl)aniline

https://huagongshe.com/ko/reaction/77699

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물1,4-DioxaneHCID 31275—
반응물N-[4-methyl-3-(9H-pyrimido[4,5-b]indol-7-yl)phenyl]-3-(trifluoromethyl)benzamideHCID 25152248—
용매WaterHCID 962—
생성물4-methyl-3-(9H-pyrimido[4,5-b]indol-7-yl)anilineHCID 6904649976.2%

반응 조건

온도100 °C

반응 단계

To N-[4-methyl-3-(9H-pyrimido[4,5-b]indol-7-yl)phenyl]-3-(trifluoromethyl)benzamide (442 mg, 0.990 mmol) was added 1,4-dioxane (2.0 mL) and water (2.0 mL) and sodium hydroxide (790 mg, 19.8 mmol). The resulting mixture was heated to 100° C. until LCMS indicated complete hydrolysis, typically 14-16 hours. The reaction was cooled to ambient temperature and the solvents were removed by evaporation. The residue was washed with water and the remaining solid was recovered by filtration, washed with additional water, and dried under reduced pressure to give the product (207 mg, 76%). 1H NMR (300 MHz, DMSO): δ 9.42 (s, 1H), 8.90 (s, 1H), 8.22 (d, 1H), 7.39 (s, 1H), 7.23 (d, 1H), 6.94 (d, 1H), 6.52 (m, 2H), 4.95 (s, 2H), 2.08 (s, 3H). MS (EI) m/z=275 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841318B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-deefaab6b7e44388a2959ca7d84573f4
출처 메모uspto-grants-2014_09