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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1944401생성일: 2026년 10월 26일

Lithium Hydroxide → [3-(2-Benzenesulfonylpyridin-3-ylmethyl)-5-fluoro-2-methylindol-1-yl]acetic acid

https://huagongshe.com/reaction/1944401

반응식

참여 물질

역할이름HCID투입량
반응물Lithium HydroxideHCID 3939—
반응물[3-(2-Benzenesulfonylpyridin-3-ylmethyl)-5-fluoro-2-methylindol-1-yl]acetic acid methyl esterHCID 67044945—
용매TetrahydrofuranHCID 8028—
생성물[3-(2-Benzenesulfonylpyridin-3-ylmethyl)-5-fluoro-2-methylindol-1-yl]acetic acidHCID 5938058670.9%

반응 단계

A mixture of [3-(2-benzenesulfonylpyridin-3-ylmethyl)-5-fluoro-2-methylindol-1-yl]acetic acid methyl ester (0.16 g) and tetrahydrofuran (5.0 mL) was treated with 1.0 M aqueous lithium hydroxide solution (0.5 mL), and the resulting mixture was stirred at room temperature for 30 minutes. The mixture was concentrated under reduced pressure, pH adjusted to 4 by the addition of 0.1 M aqueous hydrochloric acid solution and extracted with ethyl acetate. The combined organic extract was washed with saturated aqueous sodium chloride solution, dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by preparative reverse-phase HPLC, eluting with a mixture of acetonitrile and water (5:95 to 98:2 by volume) to afford the title compound as a white solid (0.11 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08394836B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-34eaa9904c9c424c84bb5be4faa2ef1c
출처 메모uspto-grants-2013_03