Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1625019생성일: 2026년 10월 26일
Potassium Hydroxide → (2R)-4-(5-Fluoro-4-iodo-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanoic acid
https://huagongshe.com/reaction/1625019
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | Ethyl (2R)-4-(5-fluoro-4-iodo-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanoate | HCID 67249679 | — |
| 용매 | Sodium Hydroxide | HCID 14798 | — |
| 용매 | Water methyl tetrahydrofuran | HCID 67831299 | — |
| 생성물 | (2R)-4-(5-Fluoro-4-iodo-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanoic acid | HCID 70664587 | 44.8% |
반응 단계
Potassium hydroxide (669 mg, 7.7 mmol) was added to a solution of ethyl (2R)-4-(5-fluoro-4-iodo-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanoate (691 mg, 1.55 mmol) in 2-methyltetrahydrofuran:water (2:1 22.5 mL) and the solution was stirred at 70° C. for 2 h. The reaction was diluted with 1 N aq NaOH (50 mL). The organics were separated and the aqueous layer was washed with EtOAc (2×50 mL), and acidified to a pH of 3 using 3 M aqueous HCl. The aqueous layer was extracted with EtOAc (3×60 mL), dried (MgSO4), filtered and concentrated to afford a yellow-white solid (290 mg, 44.8%). MS (LCMS) m/z 418.0. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.53 (s, 3 H) 2.08-2.20 (m, 1 H) 2.36-2.48 (m, 1 H) 3.13 (s, 3 H) 3.79-4.02 (m, 2 H) 7.03 (d, J=6.05 Hz, 1 H) 7.96 (d, J=4.29 Hz, 1 H) 13.82 (br. s., 1 H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08779148B2 |
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| 출처 데이터셋 | uspto-grants-2014_07 |
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| ORD ID | ord-159ec43bf4bf412b82910179d31b543a |
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| 출처 메모 | uspto-grants-2014_07 |
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