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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 273241Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/273241

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktLithium ChlorideHCID 433294—
EduktPotassium FluorideHCID 522689—
Edukt3,7-Dibromo-1,5-naphthyridineHCID 1236658—
Edukt(Z)-1-Ethoxy-2-(tributylstannyl)etheneHCID 2763294—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelTolueneHCID 1140—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-Bromo-7-[2-ethoxyvinyl]-1,5-naphthyridineHCID 6708234355%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07456196B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-8d80b49db92246b7aecd4cc2c5ec4b31
Quellennotizuspto-grants-2008_11