Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 423582생성일: 2026년 10월 25일
Potassium Carbonate → 1-Methylethyl 4-{[(6-bromo-2-fluoro-3-pyridinyl)oxy]methyl}-1-piperidinecarboxylate
https://huagongshe.com/reaction/423582
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 6-Bromo-2-fluoropyridin-3-ol | HCID 29919875 | — |
| 반응물 | Isopropyl 4-((methylsulfonyloxy)methyl)piperidine-1-carboxylate | HCID 57930057 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-Methylethyl 4-{[(6-bromo-2-fluoro-3-pyridinyl)oxy]methyl}-1-piperidinecarboxylate | HCID 86638741 | 68% |
반응 단계
1-Methylethyl 4-{[(6-bromo-2-fluoro-3-pyridinyl)oxy]methyl}-1-piperidinecarboxylate (0.238 g, 68%) was prepared as a white solid from 6-bromo-2-fluoro-3-pyridinol (0.18 g, 0.94 mmol), 1-methylethyl 4-{[(methylsulfonyl)oxy]methyl}-1-piperidinecarboxylate (prepared as in Example 131, Step 4, 0.38 g, 1.22 mmol) and K2CO3 (0.26 g, 1.88 mmol) in DMF (10 mL) in a manner similar to Example 131, Step 5. The crude product was purified by flash chromatography on an ISCO silica gel column using 0 to 35% EtOAc/hexanes. 1H NMR (400 MHz, CDCl3): δ 7.27 (d, 1H, J=8.3 Hz), 7.20-7.10 (m, 1H), 4.91 (septet, 1H, J=6.2 Hz), 4.30-4.10 (m, 2H), 3.85 (d, 2H, J=6.3 Hz), 2.85-2.70 (m, 2H), 2.10-1.95 (m, 1H), 1.90-1.75 (m, 2H), 1.45-1.20 (m, 8H); LRMS (ESI), m/z 375/377 (M+H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08101634B2 |
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| 출처 데이터셋 | uspto-grants-2012_01 |
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| ORD ID | ord-05612b188c454794affce493d80fe047 |
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| 출처 메모 | uspto-grants-2012_01 |
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