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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Benzeneethanamine, alpha-methyl-, phosphate (1:1) | HCID 62885 | — |
| 반응물 | Potassium Acetate | HCID 517044 | — |
| 반응물 | 2-Fluoropyridine-3-boronic acid | HCID 2783270 | — |
| 반응물 | 7-bromo-2-fluoro-3-(tributylstannyl)-5H-chromeno[2,3-b]pyridin-5-one | HCID 67383320 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 2-fluoro-7-(2-fluoropyridin-3-yl)-3-(tributylstannyl)-5H-chromeno[2,3-b]pyridin-5-one | HCID 67382795 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08883782B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-7adc4084163f4c1cadac176ab53a7001 |
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| 출처 메모 | uspto-grants-2014_11 |
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