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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 335906생성일: 2026년 10월 24일

Benzeneethanamine, alpha-methyl-, phosphate (1:1) → 2-fluoro-7-(2-fluoropyridin-3-yl)-3-(tributylstannyl)-5H-chromeno[2,3-b]pyridin-5-one

https://huagongshe.com/ko/reaction/335906

반응식

참여 물질

역할이름HCID투입량
반응물Benzeneethanamine, alpha-methyl-, phosphate (1:1)HCID 62885—
반응물Potassium AcetateHCID 517044—
반응물2-Fluoropyridine-3-boronic acidHCID 2783270—
반응물7-bromo-2-fluoro-3-(tributylstannyl)-5H-chromeno[2,3-b]pyridin-5-oneHCID 67383320—
용매EthanolHCID 702—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물2-fluoro-7-(2-fluoropyridin-3-yl)-3-(tributylstannyl)-5H-chromeno[2,3-b]pyridin-5-oneHCID 67382795—

반응 조건

온도85 °C

반응 단계

7-Bromo-2-fluoro-3-(tributylstannyl)-5H-chromeno[2,3-b]pyridin-5-one (0.240 g, 0.412 mmol), AmPhos (0.015 g, 0.021 mmol), potassium acetate (0.077 mL, 1.235 mmol), and 2-fluoro-3-pyridineboronic acid (0.070 g, 0.494 mmol) were suspended in a mixture of EtOH (20 mL) and water (2 mL) and heated to 85° C. After 30 minutes water (250 mL) and ethyl acetate (200 mL) were added and the phases mixed and separated. The organic was washed with 10% saturated sodium bicarbonate (100 mL) then dried with magnesium sulfate and evaporated to dryness under reduced pressure. The crude was purified using silica chromatography (hexane to ethyl acetate gradient) to give 2-fluoro-7-(2-fluoropyridin-3-yl)-3-(tributylstannyl)-5H-chromeno[2,3-b]pyridin-5-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883782B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-7adc4084163f4c1cadac176ab53a7001
출처 메모uspto-grants-2014_11