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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 273241생성일: 2026년 10월 25일

Lithium Chloride → 3-Bromo-7-[2-ethoxyvinyl]-1,5-naphthyridine

https://huagongshe.com/reaction/273241

반응식

참여 물질

역할이름HCID투입량
반응물Lithium ChlorideHCID 433294—
반응물Potassium FluorideHCID 522689—
반응물3,7-Dibromo-1,5-naphthyridineHCID 1236658—
반응물(Z)-1-Ethoxy-2-(tributylstannyl)etheneHCID 2763294—
촉매HCID 178418476HCID 178418476—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
생성물3-Bromo-7-[2-ethoxyvinyl]-1,5-naphthyridineHCID 6708234355%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456196B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-8d80b49db92246b7aecd4cc2c5ec4b31
출처 메모uspto-grants-2008_11