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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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물6-Bromo-2-fluoropyridin-3-olHCID 29919875—
반응물Isopropyl 4-((methylsulfonyloxy)methyl)piperidine-1-carboxylateHCID 57930057—
용매DimethylformamideHCID 6228—
생성물1-Methylethyl 4-{[(6-bromo-2-fluoro-3-pyridinyl)oxy]methyl}-1-piperidinecarboxylateHCID 8663874168%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101634B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-05612b188c454794affce493d80fe047
출처 메모uspto-grants-2012_01