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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Lithium Hydroxide | HCID 3939 | — |
| 반응물 | [3-(2-Benzenesulfonylpyridin-3-ylmethyl)-5-fluoro-2-methylindol-1-yl]acetic acid methyl ester | HCID 67044945 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | [3-(2-Benzenesulfonylpyridin-3-ylmethyl)-5-fluoro-2-methylindol-1-yl]acetic acid | HCID 59380586 | 70.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08394836B2 |
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| 출처 데이터셋 | uspto-grants-2013_03 |
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| ORD ID | ord-34eaa9904c9c424c84bb5be4faa2ef1c |
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| 출처 메모 | uspto-grants-2013_03 |
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