참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Lithium Chloride | HCID 433294 | — |
| 반응물 | Potassium Fluoride | HCID 522689 | — |
| 반응물 | 3,7-Dibromo-1,5-naphthyridine | HCID 1236658 | — |
| 반응물 | (Z)-1-Ethoxy-2-(tributylstannyl)ethene | HCID 2763294 | — |
| 촉매 | HCID 178418476 | HCID 178418476 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 3-Bromo-7-[2-ethoxyvinyl]-1,5-naphthyridine | HCID 67082343 | 55% |
반응 단계
A solution of 3,7-dibromo-1,5-naphthyridine (0.5 g, 1.74 mmol), tributyl-2-ethoxy-vinylstannane (1.91 mmol, 0.69 g), LiCl (8.7 mmol, 0.37 g) and 0.085 g of PdCl2(PPh3)2 in 50 mL of toluene was heated at 95° C. for 16 hr. After cooling off, 20 mL of a 2 M solution of KF was added to the mixture and stirring was continued for 0.5 hr. The mixture was diluted with 100 mL of CH2Cl2 and washed successively with a saturated solution of sodium bicarbonate, brine and water. The organic layer was dried over sodium sulfate, filtered and evaporated under reduced pressure. The residue was chromatographed using 5% MeOH in CH2Cl2 to give the desired material in 55% yield. 1H NMR (CDCl3, 300 MHz) δ 1.40 (m, 3H), 4.05 (m, 2H), 5.85 (s, 1H), 7.25 (s, 1H), 8.15 (m, 1H), 8.55 (m, 1H), 8.85 (m, 2H). MS (ESI) [M+H]+ at 280.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07456196B2 |
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| 출처 데이터셋 | uspto-grants-2008_11 |
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| ORD ID | ord-8d80b49db92246b7aecd4cc2c5ec4b31 |
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| 출처 메모 | uspto-grants-2008_11 |
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